Cochrane Database Syst Rev. 2018; 2018(3): CD001120. Monitoring Editor: Bob Woods, Bangor University, Dementia Services Development Centre Wales, Ardudwy, Holyhead Road, BangorGwyneddUK, LL57 2PZ University College London, Research Department of Clinical, Educational and Health Psychology, Gower Street, LondonUK, WC1E 6BT University of Nottingham, Institute of Mental Health, Triumph Road, NottinghamNottinghamshireUK AbstractBackgroundThis updated Cochrane Review of reminiscence therapy (RT) for dementia was first published in 1998, and last updated in 2005. RT involves the discussion of memories and past experiences with other people using tangible prompts such as photographs or music to evoke memories and stimulate conversation. RT is implemented widely in a range of settings using a variety of formats. ObjectivesTo assess the effects of RT on people living with dementia and their carers, taking into account differences in its implementation, including setting (care home, community) and modality (group, individual). Search methodsWe searched ALOIS (the Cochrane Dementia and Cognitive Improvement Group's Specialized Register) on 6 April 2017 using the search term 'reminiscence.' Selection criteriaWe included all randomised controlled trials of RT for dementia in which the duration of the intervention was at least four weeks (or six sessions) and that had a 'no treatment' or passive control group. Outcomes of interest were quality of life (QoL), cognition, communication, behaviour, mood and carer outcomes. Data collection and analysisTwo authors (LOP and EF) independently extracted data and assessed risk of bias. Where necessary, we contacted study authors for additional information. We pooled data from all sufficiently similar studies reporting on each outcome. We undertook subgroup analysis by setting (community versus care home) and by modality (individual versus group). We used GRADE methods to assess the overall quality of evidence for each outcome. Main resultsWe included 22 studies involving 1972 people with dementia. Meta‐analyses included data from 16 studies (1749 participants). Apart from six studies with risk of selection bias, the overall risk of bias in the studies was low. Overall, moderate quality evidence indicated RT did not have an important effect on QoL immediately after the intervention period compared with no treatment (standardised mean difference (SMD) 0.11, 95% confidence interval (CI) ‐0.12 to 0.33; I2 = 59%; 8 studies; 1060 participants). Inconsistency between studies mainly related to the study setting. There was probably a slight benefit in favour of RT in care homes post‐treatment (SMD 0.46, 95% CI 0.18 to 0.75; 3 studies; 193 participants), but little or no difference in QoL in community settings (867 participants from five studies). For cognitive measures, there was high quality evidence for a very small benefit, of doubtful clinical importance, associated with reminiscence at the end of treatment (SMD 0.11, 95% CI 0.00 to 0.23; 14 studies; 1219 participants), but little or no difference at longer‐term follow‐up. There was a probable slight improvement for individual reminiscence and for care homes when analysed separately, but little or no difference for community settings or for group studies. Nine studies included the widely used Mini‐Mental State Examination (MMSE) as a cognitive measure, and, on this scale, there was high quality evidence for an improvement at the end of treatment (mean difference (MD) 1.87 points, 95% CI 0.54 to 3.20; 437 participants). There was a similar effect at longer‐term follow‐up, but the quality of evidence for this analysis was low (1.8 points, 95% CI ‐0.06 to 3.65). For communication measures, there may have been a benefit of RT at the end of treatment (SMD ‐0.51 points, 95% CI ‐0.97 to ‐0.05; I2 = 62%; negative scores indicated improvement; 6 studies; 249 participants), but there was inconsistency between studies, related to the RT modality. At follow‐up, there was probably a slight benefit of RT (SMD ‐0.49 points, 95% CI ‐0.77 to ‐0.21; 4 studies; 204 participants). Effects were uncertain for individual RT, with very low quality evidence available. For reminiscence groups, evidence of moderate quality indicated a probable slight benefit immediately (SMD ‐0.39, 95% CI ‐0.71 to ‐0.06; 4 studies; 153 participants), and at later follow‐up. Community participants probably benefited at end of treatment and follow‐up. For care home participants, the results were inconsistent between studies and, while there may be an improvement at follow‐up, at the end of treatment the evidence quality was very low and effects were uncertain. Other outcome domains examined for people with dementia included mood, functioning in daily activities, agitation/irritability and relationship quality. There were no clear effects in these domains. Individual reminiscence was probably associated with a slight benefit on depression scales, although its clinical importance was uncertain (SMD ‐0.41, 95% CI ‐0.76 to ‐0.06; 4 studies; 131 participants). We found no evidence of any harmful effects on people with dementia. We also looked at outcomes for carers, including stress, mood and quality of relationship with the person with dementia (from the carer's perspective). We found no evidence of effects on carers other than a potential adverse outcome related to carer anxiety at longer‐term follow‐up, based on two studies that had involved the carer jointly in reminiscence groups with people with dementia. The control group carers were probably slightly less anxious (MD 0.56 points, 95% CI ‐0.17 to 1.30; 464 participants), but this result is of uncertain clinical importance, and is also consistent with little or no effect. Authors' conclusionsThe effects of reminiscence interventions are inconsistent, often small in size and can differ considerably across settings and modalities. RT has some positive effects on people with dementia in the domains of QoL, cognition, communication and mood. Care home studies show the widest range of benefits, including QoL, cognition and communication (at follow‐up). Individual RT is associated with probable benefits for cognition and mood. Group RT and a community setting are associated with probable improvements in communication. The wide range of RT interventions across studies makes comparisons and evaluation of relative benefits difficult. Treatment protocols are not described in sufficient detail in many publications. There have been welcome improvements in the quality of research on RT since the previous version of this review, although there still remains a need for more randomised controlled trials following clear, detailed treatment protocols, especially allowing the effects of simple and integrative RT to be compared. Plain language summaryReminiscence therapy for dementia Review question We wanted to find out what effect reminiscence therapy (RT) has on people with dementia. In particular, we were interested in effects on quality of life, communication, cognition (the general ability to think and remember), mood, daily activities and relationships. We were also interested in any effects on carers. Background RT involves discussing events and experiences from the past. It aims to evoke memories, stimulate mental activity and improve well‐being. Reminiscence is often assisted by props such as videos, pictures and objects. It can take place in a group or be done with a person on their own, when it often results in some form of life‐story book being created. RT helps older people with depression. It may be suitable for people with dementia both because depression is common in dementia and because people with dementia typically have a better memory for the distant past than for recent events. Methods We searched for randomised, controlled trials in which RT was compared with no treatment or with a non‐specific activity, such as time spent in general conversation. Our search covered all trials available up to April 2017. Results We found 22 trials with 1972 participants to include in the review. All the participants had dementia, mostly of mild or moderate severity. Some of the participants were living at home and some were in care homes. The length of the trials varied from four weeks to two years, and the overall amount of time spent on therapy varied from three to 39 hours. Overall, we thought most of the trials were well conducted. Looking at all the trials together, there did not seem to be an effect of RT on the quality of life reported by the participants. However, there was probably a slight benefit of treatment in the trials done in care homes, which was not seen in the trials done in the community. People having RT scored slightly better than the control group on tests of cognition immediately after the course of treatment, but not weeks to months later. It was not clear that the effect was large enough to be important. The effect was most evident in care home studies, which used individual RT, but not in community studies, which used group RT. We found that group RT and RT in community settings may have a positive effect on the communication and interaction of the person with dementia immediately after the end of treatment, and probably also weeks to months later, although the effect was small. Apart from a probable slight benefit of individual RT on scales measuring depressed mood, we found no evidence for effects of RT on other outcomes, such as agitation, ability to carry out daily activities or relationships with other people. We found no evidence of harmful effects of RT for the people with dementia themselves. We found no effect of RT on family carers other than a suggestion that it made carers slightly more anxious in two large studies of joint reminiscence work. In this type of RT, the carers and the people with dementia were both directly involved in the reminiscence sessions. Conclusions We were encouraged to find that the amount and quality of research on RT for dementia has increased considerably since the last version of this review. We concluded that the effects of RT vary, depending on the way it is given and whether it takes place in care homes or the community. However, there is some evidence that RT can improve quality of life, cognition, communication and possibly mood in people with dementia in some circumstances, although all the benefits were small. More research is needed to understand these differences and to find out who is likely to benefit most from what type of RT. Summary of findingsBackgroundReminiscence therapy (RT) was introduced to dementia care in the late 1970s (Kiernat 1979; Norris 1986), and has taken a variety of forms. At its most basic, it involves the discussion of past activities, events and experiences, usually with the aid of tangible prompts (e.g. photographs, household and other familiar items from the past, music and archive sound recordings). More recently, digital storage and presentation of photographs, music and video clips have become widely used (Subramaniam 2010). The development of reminiscence work is usually traced to Butler 1963's early work on "Life Review." Butler described Life Review as a naturally occurring process where the person looks back on his/her life and reflects on past experiences, including unresolved difficulties and conflicts. This concept was incorporated in psychotherapy for older people, which emphasises that life review can be helpful in promoting a sense of integrity and adjustment. Butler's seminal work contributed to the change in professional perspectives on reminiscence. Rather than being viewed as a problem, with the older person 'living in the past,' reminiscence was sees as a dynamic process of adjustment. This fitted well with Erikson 1950's late‐life stage of development, where the person is seen as reflecting on life, seeking to make sense and find meaning in a life lived. Around the same time, increasing interest in oral history meant that the reminiscences of older people were valued more greatly. In the UK, the development of the 'Recall' tape‐slide package (Help the Aged 1981) meant that reminiscence triggers were widely available in day care centres, care homes and hospitals, leading many staff to establish some form of reminiscence work, of variable quality. There was also interest in using reminiscence to guide environmental design on the basis that, for example, a lounge of a care home which resembled a living room from earlier in the person's life would seem more familiar and might lead to better maintenance of independence. It is evident that reminiscence work may take a number of different forms, from psychotherapy through to environmental redesign. There is an extensive literature on the various functions of reminiscence, with numerous classification systems proposed (e.g. Romaniuk 1981). Differences have emerged between reminiscence functions in their association with mental health, with seeking identity having a positive association and a focus on bitterness, boredom reduction and loss being associated with worse mental health (Ros 2016). In one general systematic review of reminiscence work, across a variety of populations, drawing from over 100 studies, Pinquart 2012 categorised the type of 'therapeutic work' undertaken into three broad categories: 'simple reminiscence,' involving the recall and sharing of selected personal and shared memories and stories; 'life review,' seen as a structured, evaluative process, usually conducted individually, covering the whole life story chronologically, seeking to integrate negative and positive memories; and 'life review therapy,' typically aimed at people with depression or other mental health difficulties where the aim is to re‐evaluate negative memories, promoting a more positive view of life. 'Life story work' is becoming increasingly used to describe aspects of reminiscence work, such as life review, where the emphasis is on developing a narrative biography, drawing together past, present and future. Life story books are common tangible outcomes from such work, but other media have also been used, such as a display box, portraying key elements of the person's life. Life story work has been employed with children and young people, people with learning disabilities and people with depression (Woods 2016). The type of reminiscence work undertaken has important implications for the training, supervision and support needed by those acting as facilitators or therapists. Reminiscence work, including life review, has consistently been helpful for older people with depressed mood (Bohlmeijer 2003; Pinquart 2007). The effects are comparable to both medication and other psychosocial approaches. Life review may also be helpful in preventing depression in older adults (Pot 2010), and in improving life satisfaction and quality of life (QoL) in older adults in general (Bohlmeijer 2007). The effects are also seen in older people with depressed mood living in long‐term care environments (Zhang 2015). Given that depressed mood is more common in people with dementia, reminiscence work may be helpful in dementia in relation to improving mood. In the context of dementia, reminiscence work can also be seen to have a cognitive rationale. People with dementia often appear able to recall events from their childhood, but not from more recent times, even earlier the same day. Drawing on the apparently preserved store of remote memories appears a sensible strategy, when dementia is typically accompanied by great difficulty in new learning. By linking with the person's cognitive strengths in this way, communication might be enhanced, allowing the person to talk confidently of their earlier life and experiences. In fact, studies of remote memory suggest that recall for specific events is not relatively preserved; performance across the lifespan is impaired but people with dementia, like all older people, have an 'autobiographical memory bump,' recalling more memories from youth and adolescence (Morris 1994). Some of the memories represent well‐rehearsed, much practised items or anecdotes. The almost complete absence of autobiographical memories from the person's middle years could lead to a disconnection of past and present, which could contribute to the person's difficulty in retaining a clear sense of personal identity. From a cognitive standpoint, autobiographical memory and level of communication appear key outcomes. Since the first study on reminiscence work that was conducted with a group of older people with dementia was reported by Kiernat 1979, the approach has continued to be implemented widely, in a variety of forms. However, the research literature has developed more slowly. The 2005 version of this review included only four studies, and several of them were of low quality. In a more recent review, Cotelli 2012 also highlighted the absence of high quality studies. Subramaniam 2012 focused on individual reminiscence work in their systematic review, identifying five randomised controlled trials (RCT), mainly with small sample sizes. The distinction between 'simple' reminiscence and 'life review,' often leading to the production of a life story book, appeared salient in these reviews. Simple reminiscence may be on an individual or a group basis, whereas life review is typically conducted individually. The involvement of family carers in reminiscence groups jointly with people with dementia is a further development, using simple reminiscence but potentially having an effect on pre‐existing relationships (Bruce 1998; Thorgrimsen 2002). The implications of this background for the current review are as follows.
ObjectivesTo assess the effects of RT on people living with dementia and their carers, taking into account differences in its implementation, including setting (care home, community) and modality (group, individual). MethodsCriteria for considering studies for this reviewTypes of studiesStudies had to meet the following criteria.
Trials that did not publish (or later supply) adequate information about study design and results were included in the review but not in the meta‐analysis. Details are noted in Characteristics of included studies. Types of participantsWe included:
We excluded:
Types of interventions
Types of outcome measures
Outcomes for the person with dementiaPrimary outcome
Secondary outcomes
Outcomes of interest for the person with dementia were measured using standardised instruments to determine if changes in these outcomes were observed following the intervention. This included self‐reported ratings, clinical ratings or carer ratings of the outcome. Outcomes for the carer'Carer' in these contexts refers to family carers and professional carers, although they were considered separately in the review.
Adverse outcomesThere is a potential risk that the process of recalling memories from the past may bring about difficult or emotional (or both) memories, which should be anticipated and managed sensitively by facilitators. The potential for adverse outcomes was monitored by observing negative responses on the outcome measures. Family carers or care staff hold their own perceptions of the intervention and its effect on the participant, as well as on themselves, which will be reflected in their carer‐rated outcome measures. Search methods for identification of studiesElectronic searchesWe searched ALOIS (www.medicine.ox.ac.uk/alois), the Cochrane Dementia and Cognitive Improvement Group's Specialized Register on 6 April 2017. The search term used was 'reminiscence.' ALOIS was created in part thanks to a grant from the American Alzheimer's Association and is maintained by the Information Specialists of the Cochrane Dementia and Cognitive Improvement Group. It contains studies in the areas of dementia prevention, dementia treatment and cognitive enhancement in healthy older populations. The studies are identified from:
To view a list of all sources searched for ALOIS see About ALOIS on the ALOIS website. Details of the search strategies used for the retrieval of reports of trials from the healthcare databases, CENTRAL and conference proceedings can be viewed in the 'methods used in reviews' section within the editorial information about the Dementia and Cognitive Improvement Group. Additional searches (6 April 2017) were performed in many of the sources listed above to cover the timeframe from the last searches performed for ALOIS to ensure that the search for the review was as up‐to‐date and comprehensive as possible. See Appendix 1 for search strategies. Searching other resources
Additionally, we searched the reference lists of all papers for further references, and review authors searched personal holdings of references to reports and trials. We sent letters/e‐mails to all authors of included RCTs asking for essential information, where this was not available in the publication (e.g. statistics or details of randomisation, or both). Data collection and analysisSelection of studiesFollowing deduplication, two review authors (LOP and EF) independently reviewed the abstracts and, if necessary, the manuscripts of potential studies identified by the search. These review authors were not involved in any of the studies produced by the searches. We excluded obviously irrelevant studies. We obtained the full text of remaining studies and excluded studies that did not meet the inclusion criteria with reasons outlined in the Characteristics of excluded studies table. If authors disagreed about the inclusion of a particular study, this was referred to another review author (BW or AS) for clarification. We collated multiple reports of the same study, so that each study, rather than each report, was the unit of interest in the review. We recorded the selection process in sufficient detail to complete a PRISMA flow diagram (Figure 1). Data extraction and managementTwo review authors (EF and LOP) independently extracted descriptive characteristics, study methodology data and study results from the included studies, recorded them on a data collection form and entered them into Review Manager 5 (RevMan 2014). The form was piloted on ten studies. We compared the data to ensure accuracy. Where data did not match, one review author (LOP) checked the data of both authors and made changes if necessary with the agreement of another review author (EF). For each outcome measure, the authors sought to obtain data on every participant randomised irrespective of whether the participant was excluded or dropped out of the intervention or research (i.e. data from an intention to treat (ITT) analysis). If these data were not available in the published studies, the review authors sought the data of those who completed the trials. Where necessary, we sent emails to trial authors requesting additional information. If this was unsuccessful, we contacted authors through ResearchGate. Assessment of risk of bias in included studiesTwo review authors (LOP and EF) independently assessed the risk of bias of each trial using the Cochrane 'Risk of bias' tool (Higgins 2011). We attempted to obtain additional information from study authors when we required further information. Based on the methods detailed in the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011), we classified each category of bias as 'low risk of bias,' 'high risk of bias' or 'unclear risk of bias.' An outline of this can be seen in Table 1 below. The meta‐analysis included only trials with a low or unclear risk of bias, except in the case of random sequence generation where only trials with a low risk of bias were included. Any disagreements regarding risk of bias ratings were referred to an independent review author (AS) for clarification. Overall ratings were assigned with respect to each study's methodological quality and are described in the 'Risk of bias' table, Figure 2; and Figure 3. Risk of bias summary: review authors' judgements about each risk of bias item for each included study. Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
RT: reminiscence therapy. Measures of treatment effectData from all included studies were continuous. This type of data required the mean change scores from baseline, the standard deviation of the mean change and the number of participants for each treatment group at each assessment. The majority of study authors did not report change scores from baseline. The baseline assessment was defined as the latest available assessment prior to randomisation, but no longer than two months prior. Where change scores were not reported, the review authors extracted the mean, standard deviation and number of participants for each treatment group at each time point and calculated the required summary statistics manually. In this case, a zero correlation between the measurements at baseline and assessment time was assumed. This method overestimates the standard deviation of the change from baseline, but this conservative approach is considered to be preferable in a meta‐analysis. The meta‐analyses included the combination of data from trials that may not have used the same rating scale to measure a particular outcome. For example, cognition may have been measured by the MMSE in one study and the Autobiographical Memory Interview (AMI) in another. In this situation, the standardised mean difference (SMD; the absolute mean difference (MD) divided by the standard deviation) was used to measure the treatment difference. Where pooled trials used the same rating scale or test to measure an outcome, the MD was used. To allow comparisons with other scales assessing similar outcomes, it was necessary to reverse the change scores on certain scales. For example, on measures of depression where a low score was indicative of a positive outcome on one scale and a high score was indicative of a positive outcome on another. Unit of analysis issuesIn studies using a cross‐over design, only data from the first treatment phase after randomisation were eligible for inclusion. Where studies used cluster randomisation and were large, one review author (LOP) extracted the mean size of each cluster, the mean and standard deviation summary statistics, and the estimated intraclass correlation coefficient (ICC) in order to reduce the size of the trial to its effective sample size. This was carried out following Cochrane guidelines set out in the Cochrane Handbook for Systematic Reviews of Interventions. Where studies were not large enough, this could not be carried out. Cluster trials were also assessed for additional biases associated with clustering, including recruitment bias; baseline imbalance; loss of clusters and comparability with individually randomised trials. Dealing with missing dataWhere possible, review authors extracted data on all participants randomised. Data from ITT analyses were preferred to per protocol or compliance analyses. Assessment of heterogeneityAssessments of heterogeneity were performed using both the Chi2 and I2 statistic. Review authors followed guidance in the Cochrane Handbook for Systematic Reviews of Interventions to interpret heterogeneity percentages (i.e. 0% to 40% might not be important; 30% to 60% may represent moderate heterogeneity, 50% to 90% may represent substantial heterogeneity; and 75% to 100% is considerable heterogeneity). Assessment of reporting biasesIf there were enough studies available, authors created a funnel plot to assess the risk of publication bias. Data synthesisThe meta‐analyses presented overall estimates of the treatment difference using a fixed‐effect model. Where there was evidence of high heterogeneity of the treatment effect between trials, we used a random‐effects model (which results in broader CIs than a fixed‐effect model). Subgroup analysis and investigation of heterogeneitySubgroup analyses were performed where possible to assess for any important differences related to environmental context or the type/modality of the reminiscence intervention. Assessments of heterogeneity were performed using both the Chi2 test and I2 statistic. Where heterogeneity was high, we used a random‐effects model (rather than a fixed‐effect model). Sensitivity analysisWhere necessary, sensitivity analyses were carried out. For example, when meta‐analysing carer scores on the Zarit Burden Interview (ZBI), a sensitivity analysis was carried out depending on the level of carer involvement in the intervention. Presentation of results and 'Summary of findings' tablesWe used GRADE methods to rate the quality of evidence (high, moderate, low or very low) behind each effect estimate in the review (Guyatt 2011). This rating referred to our level of confidence that the estimate reflected the true effect, taking account of the risk of bias in the included studies, inconsistency between studies, imprecision in the effect estimate, indirectness in addressing our review question and the risk of publication bias. We produced 'Summary of findings' tables for RT compared to no treatment to show the effect estimate and the quantity and quality of the supporting evidence for the following outcomes:
We produced additional tables to summarise the effects on QoL, communication and interaction, and cognition for the two different settings for reminiscence work included in this review (community and care home settings) and for the two major modality types (individual reminiscence work and reminiscence groups). We prepared the 'Summary of findings' tables using the GRADEpro GDT 2015 (gradepro.org). ResultsDescription of studiesSee: Characteristics of included studies; Characteristics of excluded studies; and Characteristics of ongoing studies tables. Results of the searchSystematic searches conducted since the previous review up to October 2014 identified 102 potentially eligible trials, of which 11 were included. A further search conducted in April 2015 identified 21 potential trials. One of these met the inclusion criteria, but was only available as a conference paper (Dwolatzky 2014). Later, in April 2016 another search returned 25 records, with three eligible for inclusion. A final search in April 2017 yielded 37 results, of which two were eligible for inclusion. This gave a total of 21 trials that met the inclusion criteria. Two trials by the same authors were identified (Tadaka 2004; Tadaka 2007), and further examination showed that the same data set and outcome measures were used in both papers. As the data from the earlier paper were not in usable form, the more recent paper, which presented the results as a comparison of AD and VD was included (Tadaka 2007), and the earlier paper (Tadaka 2004) was excluded. Because Tadaka 2007 analysed the two participant groups separately, with a different control group for each disease type, we entered this study into the meta‐analysis as two separate RCTs (Tadaka 2007 (AD); Tadaka 2007 (VD)), bringing the number of included studies to 22. More information can be found in the study flow diagram (Figure 1). Included studiesThe review included 22 studies, with 1972 participants: 1001 participants were randomised to treatment conditions and 971 participants to control conditions. In addition to the five studies in our previous 2005 review (Baines 1987; Goldwasser 1987; Lai 2004; Morgan 2012; Thorgrimsen 2002) (of which the Morgan 2012 study is now a published article rather than a doctoral thesis), 17 new studies met the inclusion criteria (Akanuma 2011; Amieva 2016; Azcurra 2012; Charlesworth 2016; Gonzalez 2015; Haight 2006; Hsieh 2010; Ito 2007; Melendez 2015; O'Shea 2014; Särkämö 2013; Subramaniam 2013; Tadaka 2007 (AD); Tadaka 2007 (VD); Woods 2012a; Yamagami 2012; Van Bogaert 2016). We excluded six of the included studies from the meta‐analyses (Akanuma 2011; Baines 1987; Goldwasser 1987; Gonzalez 2015; Hsieh 2010; Yamagami 2012). All six studies were at unclear risk of selection bias due to inadequate information about random sequence generation and allocation concealment. This was the main reason they were excluded, although all six were also rated at unclear risk of bias in at least one other domain. The risk of bias details for each study are summarised in the Risk of bias in included studies tables while Figure 2 depicts the risk of bias summary. Considering that the Baines 1987 and Goldwasser 1987 studies dated from the 1980s, we did not attempt to contact the study authors. Furthermore, in the previous versions of this review, we were unable to get in touch with the authors of the Goldwasser 1987 study. We attempted to contact the authors of the Akanuma 2011; Gonzalez 2015; Hsieh 2010; and Yamagami 2012 studies for more information, but there was no response. Full details of included studies are presented in the Characteristics of included studies table and reasons for exclusion of studies in the Characteristics of excluded studies table. DesignAll studies were described by their authors as RCTs, although, as noted above, six studies did not provide enough information on the randomisation methods for us to be sure that the risk of selection bias was low. One study was a cross‐over trial (Baines 1987). There were three cluster randomised trials (Gonzalez 2015; Melendez 2015; O'Shea 2014). Dementia typeSix studies recruited participants with a specific type of dementia diagnosis. Four studies only recruited participants with a diagnosis of AD (Amieva 2016; Azcurra 2012; Gonzalez 2015; Melendez 2015), although Melendez 2015 also recruited a separate group of participants with amnesic MCI, and two studies sought only participants with a diagnosis of VD (Akanuma 2011; Ito 2007). Tadaka 2007 recruited both participants with AD and VD, but analysed the two groups separately, with a different control group for each disease type. Dementia severityThe majority of included studies sought to recruit participants in the mild to moderate stages of dementia. However, Gonzalez 2015 and Melendez 2015 only included people with mild AD as measured by a score of 3 or 4 on the Geriatric Depression Scale (GDS; i.e. mild dementia was the maximum level). Five studies did not specify a particular level of severity in their inclusion/exclusion criteria (Goldwasser 1987; Haight 2006; Lai 2004; Thorgrimsen 2002; Yamagami 2012). Six studies used the CDR as a screening measure to assess if participants met the inclusion criteria. Five studies required a score of between 1 and 2 (mild to moderate dementia) to participate (Morgan 2012; Subramaniam 2013; Tadaka 2007 (AD); Tadaka 2007 (VD); Woods 2012a), while potential participants in one study needed to score between 0.5 and 2 (questionable to moderate dementia) (Särkämö 2013). Nine studies reported baseline CDR scores. Azcurra 2012 reported a mean score of 1 and Särkämö 2013 reported a mean score of 1.35, indicating that participants had mild‐to‐moderate dementia. Seven studies reported (or sent the review authors) the number of participants who achieved each score. Across five studies, approximately 65% of participants obtained a score of 1 on the CDR indicating that they had mild dementia, while 35% scored 2 indicating moderate dementia (Hsieh 2010; Morgan 2012; Subramaniam 2013; Tadaka 2007 (AD); Tadaka 2007 (VD)). One study used the CDR sum of boxes as an outcome measure and baseline CDR scores indicated that nine participants had 'questionable dementia', 24 had mild dementia, 17 had moderate dementia and four had severe dementia (Yamagami 2012). Woods 2012a indicated that 6.2% of his participants scored 0.5, 67.4% scored 1 and 26.5% scored 2. Sixteen studies reported MMSE scores at baseline. This included one study that used the Hasegawa Dementia Scale‐Revised (the authors reported this was similar to the MMSE) (Yamagami 2012). One study used the Cantonese version of the MMSE (Lai 2004), while two studies used the Spanish version (Gonzalez 2015; Melendez 2015). Although published cut‐off points on the MMSE should be interpreted cautiously, a widely cited study classified an MMSE score of less than 10 as severe impairment, 10 to 20 as moderate impairment and 20 to 25 as mild impairment (Folstein 1975). In 13 studies, the mean MMSE score fell within the moderate range (Azcurra 2012; Charlesworth 2016; Goldwasser 1987; Gonzalez 2015; Haight 2006; Ito 2007; Melendez 2015; O'Shea 2014; Särkämö 2013; Tadaka 2007 (AD); Tadaka 2007 (VD); Thorgrimsen 2002; Van Bogaert 2016; Yamagami 2012), and in one study the mean MMSE score fell within the severe range (Lai 2004). Recruitment settingIncluded studies recruited participants from a range of settings including residential care facilities, local hospitals, day hospital facilities and outpatient clinics. Fourteen studies recruited participants from residential/hospital care settings, while eight recruited community‐dwelling participants (Amieva 2016; Charlesworth 2016; Melendez 2015; Särkämö 2013; Tadaka 2007 (AD); Tadaka 2007 (VD); Thorgrimsen 2002; Woods 2012a). The interventions took place in the care homes where participants resided or community locations such as day centres. Participant ageThe mean age of participants was over 80 years, with the exception of participants in three studies where reported mean ages were 78 years (Akanuma 2011), 77 years (Särkämö 2013), and 78 years (Woods 2012a). One study reported age range of 60 to 99 years (Haight 2006), and one study reported the median participant age and interquartile range (IQR) as 84 years (78 to 90 years) (Van Bogaert 2016). Length and duration of interventionsThe length of reminiscence interventions ranged from four weeks (the minimum number for inclusion in the review) to 24 months. For studies that reported a range of time for each session (e.g. 60 to 90 minutes), we took the median time to calculate exposure time and session length. The intervention delivered at the highest frequency each week was 30 minutes a day, five days a week, for four weeks (Baines 1987). Six other studies reported session frequencies of more than once a week (Azcurra 2012; Goldwasser 1987; Melendez 2015; O'Shea 2014; Van Bogaert 2016; Yamagami 2012). The greatest possible reminiscence exposure time was 39 hours (Amieva 2016). Participants received 90 minutes of reminiscence a week for 12 weeks, followed by six‐weekly maintenance sessions for the next 21 months. Two studies had a possible exposure time of 38 hours (Charlesworth 2016; Woods 2012a). In both studies, participants received weekly two‐hour reminiscence sessions for 12 weeks, followed by monthly reminiscence maintenance sessions for seven months, giving a total of 38 potential hours of RT. In the Charlesworth 2016 study, the family carers met separately from the main group for 45 minutes for four sessions, with the aim of developing listening and communication skills, and considering how the activities and strategies in the sessions could continue at home. The least intensive intervention was weekly 30‐minute sessions for six weeks, totalling three hours of possible exposure to reminiscence (Lai 2004). All other studies delivered the intervention once a week for varying lengths of time. For two studies, the length of reminiscence sessions, and, therefore, potential reminiscence exposure time was unclear (O'Shea 2014; Thorgrimsen 2002). Across the remaining included studies, the median intervention exposure time was 11.5 hours. The median individual session length was approximately 53 minutes with a range of 30 minutes to two hours per session. Control group activitiesParticipants in control conditions were either assigned to a 'treatment as usual' condition or a social contact group involving general unstructured conversion. Some trials included additional conditions as well as a no‐treatment control condition. However, we used only the no‐treatment control in our analyses. For example, one study had an additional 'music singing group' (Särkämö 2013), while another study had included a counselling condition (Azcurra 2012). One study used a factorial design with four conditions, but we included only data from the RT only and treatment as usual groups (Charlesworth 2016). Similarly, another study had four conditions, but we extracted data only from the reminiscence and control conditions (Amieva 2016). One study had a 'gift' condition whereby a family member of participants in the control group made a life story book for them without their knowledge. We included data from the first follow‐up time point (i.e. before the life story books were given to participants) in the review, as the 'gift' condition was effectively a no treatment control condition until the participants received their life story books (Subramaniam 2013). Excluded studiesIn preparing this up‐dated review, we excluded 63 studies that did not meet all necessary inclusion criteria (see Characteristics of excluded studies table). Reasons for the exclusion of studies varied. The most common reasons were no or inadequate randomisation (meaning the study was not an RCT), intervention was not reminiscence or studies did not specifically recruit participants with a diagnosis of dementia. Risk of bias in included studiesSpecific details of the risk of bias for each study are outlined in the 'Risk of bias' table and are summarised in Figure 2 and Figure 3. Allocation13 studies were at low risk of selection bias, while nine were rated as unclear. Most studies reported randomisation methods although allocation concealment was rarely reported in detail. Where necessary, we contacted authors for clarification. Replies generally stated that adequate concealment of treatment allocation had been applied, without detailing the method. In these cases, good practice has been assumed, though it was regrettable that further details were not available. Three studies used an accredited trials unit to randomise and allocate participants to their respective conditions (Charlesworth 2016; Subramaniam 2013; Woods 2012a). Three studies used cluster randomisation. One large scale study used cluster randomisation stratified by public or private residential units (O'Shea 2014). Two studies recruited participants in two nursing homes and then randomly allocated the nursing homes to the treatment and control conditions (Gonzalez 2015; Melendez 2015). BlindingPerformance biasParticipants cannot be blinded to the experience of taking part in an intervention and likewise, control participants will be aware that they have entered a research trial, but are not receiving any treatment. The person's expectations of potential benefits, or otherwise, may well influence outcome measures, which is difficult to control for. Detection biasEight studies were at unclear risk of detection bias (Goldwasser 1987; Gonzalez 2015; Haight 2006; Hsieh 2010; Morgan 2012; Tadaka 2007 (AD); Tadaka 2007 (VD); Yamagami 2012). However, fourteen studies took adequate measures to blind outcome assessors and were at low risk of detection bias. Two studies asked assessors to record their prediction of which arm of the trial each participant belonged to, and their confidence in that prediction (Charlesworth 2016; Woods 2012a). In the Woods 2012a study, in 44% of cases, interviewers felt participants could equally have been assigned to control or treatment group, with 23% making a correct definite judgement. The proportion of correct definite judgements remained low at follow‐up, at about 25%, which reflected the considerable degree of uncertainty around treatment allocation. Charlesworth 2016 reported a similar prediction pattern. Measures of behaviour, functioning and carer‐rated outcomes of mood and QoL were typically completed by a person who knew the participant and could reliably comment. Incomplete outcome dataEighteen studies were at low risk of attrition bias, while four were at an unclear risk. Data extracted from several studies were from ITT analyses (Amieva 2016; Azcurra 2012; Charlesworth 2016; Lai 2004; Melendez 2015; O'Shea 2014; Woods 2012a). Eight studies used a per protocol analysis where the analysis was completed without data from participants who dropped out (Hsieh 2010; Ito 2007; Särkämö 2013; Subramaniam 2013; Tadaka 2007 (AD); Tadaka 2007 (VD); Van Bogaert 2016; Yamagami 2012). In the Ito 2007 study, both a per protocol and ITT analysis were completed, but we could only extract data from the per protocol analysis. Four studies reported zero withdrawals (Baines 1987; Haight 2006; Morgan 2012; Thorgrimsen 2002). In one study, one participant dropped out, so the authors randomly excluded one participant from each of the two other groups (Goldwasser 1987). All trials, apart from Gonzalez 2015, reported attrition rates. The largest care home study, which was based in residential care homes across Ireland, reported 25/153 withdrawals (16%) in the intervention group and 27/151 (18%) in the control group, with withdrawals predominantly due to hospitalisation, transfer to a different residential home or the death of the participant (O'Shea 2014). The largest community‐based study reported a slightly higher attrition rate with 137 total withdrawals from the trial (23% from the treatment group and 34% from the control group) (Woods 2012a). Reasons cited were wide ranging and included death or illness of participant or carer, not enough time, or no explanation given. A total of 79/291 participants (27%) were lost over the duration of the Charlesworth 2016 study, for varying reasons including carer in poor health and loss to contact. Selective reportingThere was no evidence of selective outcome reporting for any study. All studies reported the same outcome measures in the methods and results sections of papers. Four studies had a protocol and the outcome measures detailed in the protocol were reported in the completed papers (Charlesworth 2016; O'Shea 2014; Van Bogaert 2016; Woods 2012a). Other potential sources of biasTreatment protocolThe previous version of this review recommended that future trials should follow a clear treatment protocol, so that it is possible to define precisely the key elements of the different approaches to reminiscence work. The presence of a treatment protocol, or at least evidence of a session plan, is imperative to ensure that the intervention is delivered correctly, and to prevent intervention 'drift' (where the theme of the session may drift off‐topic), or introduce unintentional bias. Seventeen studies were at a low risk of bias relating to the presence of a treatment protocol, while five were at an unclear risk. Seven studies used a standardised reminiscence format. Three of these used the Haight 1992 Life Review Model and Life Review Experience Form, which provides a structured format for obtaining relevant information from participants (Haight 2006; Morgan 2012; Subramaniam 2013). The Woods 2012a, Charlesworth 2016 and Thorgrimsen 2002 studies followed 'Remembering Yesterday, Caring Today' (RYCT; Schweitzer 2008), which is a large group‐based approach, bringing people with dementia and family carers together with a focus on active reminiscence.The Van Bogaert 2016 study based their reminiscence intervention on the SolCos model (Soltys 1994). Facilitator training and supervisionWe considered the knowledge of staff delivering the interventions, total training hours and availability of supervision. All studies were at a low risk of bias in relation to facilitator training and supervision. Eleven studies did not specify training (Akanuma 2011; Goldwasser 1987; Gonzalez 2015; Hsieh 2010; Ito 2007; Melendez 2015; Morgan 2012; Särkämö 2013; Subramaniam 2013; Tadaka 2007 (AD); Tadaka 2007 (VD)), but all were reported to have been delivered by appropriate facilitators such as psychologists or gerontologists. Further details are available in the 'Risk of bias' table. The other studies provided four hours (Yamagami 2012), six hours (Baines 1987), 10 hours Haight 2006, 19.3 hours (Lai 2004), 22 hours (Thorgrimsen 2002), 30.4 hours (Azcurra 2012), one day (Charlesworth 2016), two and a half days (Woods 2012a), and three days (Amieva 2016; O'Shea 2014) of training. Facilitators in the Van Bogaert 2016 study received a training programme though the total number of hours was not specified. ContaminationThe main risk of contamination arose from trials located in care homes, in which control and intervention participants resided and socialised together. Two studies that included residential care participants seemed to use at least one member of staff or research team to carry out the intervention whilst also working in the home, potentially meaning that themes of reminiscence could be carried over into daily care and contaminate any control conditions (Goldwasser 1987; Haight 2006). However, correct adherence to the trial protocol would have minimised this risk. Outcome measuresWhere more than one measure of a single outcome domain was used in a study, data from the most common or the most extensive measure were included in the meta‐analysis. This was to avoid including data from the same participants more than once in each outcome analysis. Most studies collected outcomes up to two weeks after the final session, but for some larger studies this may have been up to four weeks (Charlesworth 2016; Woods 2012a). For purposes of this review, the primary end points of the Amieva 2016; Charlesworth 2016; and Woods 2012a studies were after the 12 weeks of weekly reminiscence sessions (three months post‐baseline) while the later follow‐up time point was following completion of the monthly maintenance sessions. Quality of life Ten studies measured self‐reported QoL at the end of treatment time point, while six measured it at follow‐up. Two were excluded from the meta‐analysis for risk of selection bias (Baines 1987; Gonzalez 2015), while the Subramaniam 2013 follow‐up data were also not included because the control group condition had changed by then (participants had been given a life story book as a gift). In the meta‐analysis, all studies used the Quality of Life in Alzheimer's Disease (QoL‐AD), except for the Azcurra 2012 study, which used the Self‐Report Quality of Life (SR‐QoL) scale. Seven studies measured proxy‐rated QoL. The Baines 1987 and Goldwasser 1987 studies were excluded from the meta‐analysis for risk of selection bias. All used the proxy scale on the QoL‐AD. Three studies went on to measure it at follow‐up. Two studies measured observed QoL using the Well‐being/Ill‐being (WIB) scale at both end of treatment and follow‐up (Azcurra 2012; Lai 2004). Cognition Nineteen studies measured cognition at end of treatment. Five studies at unclear risk of selection bias (Akanuma 2011; Baines 1987; Goldwasser 1987; Gonzalez 2015; Yamagami 2012), and follow‐up data from Subramaniam 2013 were excluded. Eight studies were included in the meta‐analysis at follow‐up. The most commonly used measures in the meta‐analysis were the MMSE (nine studies) and the Autobiographical Memory Interview Extended Version (AMI‐E) (four studies). Communication and Interaction Eight studies measured communication and interaction at end of treatment with four assessing it at a later follow‐up time point. Two studies were excluded from the meta‐analysis for risk of selection bias (Baines 1987; Yamagami 2012). The meta‐analysis included data from four outcome measures; the Holden Communication Scale (Thorgrimsen 2002), Social Engagement Scale (SES) (Azcurra 2012; Lai 2004), Multidimensional Observation Scale for Elderly Subjects (MOSES) withdrawal subscale (Tadaka 2007 (AD); Tadaka 2007 (VD)), and the Communication Observation Scale for Cognitive Impaired (Haight 2006). The follow‐up meta‐analysis was comprised of data from the SES (Azcurra 2012; Lai 2004) and MOSES (Tadaka 2007 (AD); Tadaka 2007 (VD)) Quality of caring relationshipThree studies evaluated the quality of the relationship between the carer and the person with dementia (as rated by the person with dementia) at the end of treatment (Charlesworth 2016; Subramaniam 2013; Woods 2012a). All three used the Quality of Carer and Patient Relationship (QCPR), which has two subscales: warmth and absence of conflict. The Charlesworth 2016 and Woods 2012a studies measured this again at a follow‐up time point. Behaviour We divided measures of behaviour into measures of function (i.e. daily living skills) and measures of agitation/irritability. Four studies used scales which assess both of these domains (MBS, CAPE, Behavior Rating Scale for the Elderly (BRSE)) (Akanuma 2011; Baines 1987; Haight 2006; Thorgrimsen 2002). As the authors were unable to extract scores for each, data from these two outcome measures were not included in the meta‐analysis. Behaviour: agitation/irritabilityFour studies measured agitation/irritability (O'Shea 2014; Tadaka 2007 (AD); Tadaka 2007 (VD); Yamagami 2012), though one was excluded from the meta‐analysis as there was a high risk of selection bias (Yamagami 2012). The Tadaka 2007 (AD) and Tadaka 2007 (VD) studies used the irritability subscale of the MOSES at end of treatment and follow‐up, while the O'Shea 2014 study used the Cohen Mansfield Agitation Inventory (CMAI) at end of treatment only. The Ito 2007 study also measured agitation/irritability using the MOSES but did not report the scores obtained on each subscale. Therefore, the MOSES data from this study could not be included in this meta‐analysis. Mood‐related outcomes (person with dementia) AnxietyTwo studies measured anxiety at end of treatment and follow‐up using the Hospital Anxiety and Depression Scale (HADS) ‐ Anxiety subscale (Charlesworth 2016) and Rating Anxiety In Dementia (RAID) scale (Woods 2012a). ApathyTwo studies measured apathy at end of treatment; Amieva 2016 used a carer rated Apathy Index and Hsieh 2010 used the Apathy Evaluation Scale, but the latter study was excluded from the meta‐analysis for risk of selection bias. Carer outcomes Carer outcomes were divided into outcomes measuring stress related to caring, carer anxiety and depression, carer QoL, and the quality of the caring relationship. Carer depression and anxietyTwo studies measured carer depression and anxiety at end of treatment and follow‐up (Charlesworth 2016; Woods 2012a). Both studies used the HADS. These subscales were analysed separately. Carer well‐being and quality of lifeFour studies measured carer well‐being and QoL at end of treatment (Charlesworth 2016; Särkämö 2013; Thorgrimsen 2002; Woods 2012a). Only the Thorgrimsen 2002 study did not include a follow‐up measure. The meta‐analysis comprised of data from the 12‐item General Health Questionnaire (GHQ‐12), 28‐item General Health Questionnaire (GHQ‐28) and the 12‐item Short Form (SF‐12) Mental component. Quality of caring relationshipThree studies evaluated the quality of the relationship between the carer and the person with dementia (as rated by the carer) at the end of treatment (Charlesworth 2016; Subramaniam 2013; Woods 2012a). All three used the Quality of Carer and Patient Relationship (QCPR), which has two subscales: warmth and absence of conflict. The Charlesworth 2016 and Woods 2012a studies measured this again at a follow‐up time point. Effects of interventionsSee: Table 1; Table 2; Table 3 Summary of findings for the main comparisonReminiscence Therapy compared to no treatment for people living with dementia
Summary of findings 2Reminiscence therapy compared to no treatment for people living with dementia (modality)
Summary of findings 3Reminiscence therapy compared to no treatment for people living with dementia (setting)
Effect sizesEvaluating the clinical meaningfulness of changes on the outcome measures used in studies of reminiscence interventions is challenging, as there are no internationally agreed standards to apply in this context. For SMDs, we have adopted the rule that an SMD of 0.5 or greater reflects an important difference, with SMDs less than 0.10 being negligible. For analyses using the MMSE, we judged a difference of 1.5 points or more as clinically important. The rate of decline on this measure has been estimated, in mild to moderate dementia, to be between 2 and 4 points per annum (Mohs 2000), and so 1.5 points is broadly equivalent to preventing six months of decline in cognition. For other measures, we did not have parallel criteria, so have applied the 0.5 of a standard deviation rule, taking the standard deviation from the baseline evaluations. Thus, for the QoL‐AD, we have taken a difference of 3 points or more to be clinically meaningful, reflecting approximately half the typical standard deviation in samples of people with mild to moderate dementia (e.g. Woods 2012a). For the SR‐QoL, this translates to 2.2 points or more (Azcurra 2012); for the WIB, 0.3 points or more (Azcurra 2012; Lai 2004); for the MOSES Withdrawal Scale, 3.1 points or more (Tadaka 2007); for the SES, 0.75 points or more (Azcurra 2012); for the QCPR warmth and absence of conflict scales, rated by the person with dementia, 1.8 points; for the MOSES Irritability Scale, 2.2 points or more (Tadaka 2007); for the ZBI 3 points or more (Azcurra 2012); for HADS ‐ Anxiety, 2.2 points or more; for HADS ‐ Depression, 1.8 points or more (Woods 2012a); for the QCPR rated by the carer: warmth 2.7 points or more, absence of conflict 2.2 points or more. Outcomes for the person with dementiaQuality of life(See Figure 4.) Forest plot of comparison: 1 Reminiscence therapy versus no treatment, outcome: 1.1 Self‐reported quality of life post‐treatment. For the overall evaluation of the effects of reminiscence on QoL at the end of treatment, eight studies reporting a self‐report QoL measure were included in the meta‐analysis (Amieva 2016; Azcurra 2012; Charlesworth 2016; O'Shea 2014; Särkämö 2013; Subramaniam 2013; Thorgrimsen 2002; Woods 2012a). This included 1060 participants living with dementia; 595 received a reminiscence intervention and 465 received no treatment. Where studies used more than one measure of QoL, the analysis was conducted on the most common or extensive self‐report assessment; seven studies used the QoL‐AD (self‐report) and one study used the SR‐QoL. A random‐effects analysis resulted in a small overall effect size (SMD 0.11, 95% CI ‐0.12 to 0.33; I2 = 59%; moderate quality evidence; Analysis 1.1). This indicated that, across the eight included studies, reminiscence did not have an important effect on self‐reported QoL. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 1 Self‐reported quality of life post‐treatment. Five studies (all involving reminiscence groups) went on to measure the effects of reminiscence on QoL at later follow‐up of six to 21 months (Amieva 2016; Azcurra 2012; Charlesworth 2016; Särkämö 2013; Woods 2012a). This analysis involved 499 participants who received a reminiscence intervention and 375 who received a control intervention. We could not determine whether reminiscence was associated with any effect on self‐reported QoL at follow‐up. The results were inconsistent between studies and the result of the meta‐analysis was imprecise and compatible with either an improvement or a small detrimental effect (random‐effects analysis; SMD 0.35, 95% CI ‐0.11 to 0.80; I2 = 89%; moderate quality evidence; Analysis 1.17). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 17 Self‐reported quality of life at follow‐up. At both end of treatment and follow‐up there was substantial heterogeneity, which appeared to relate to different modalities and (particularly) contexts of reminiscence work being analysed together. Analyses were accordingly undertaken for different modalities and contexts separately. ModalityOne small study reported self‐report QoL outcomes for individual reminiscence interventions at end of treatment (Subramaniam 2013). This involved 23 participants, and indicated life story work may have improved self‐reported QoL‐AD (mean difference (MD) 7.00 points, 95% CI ‐0.14 to 14.14; low quality evidence). Of the seven studies that implemented group reminiscence interventions, including 1037 participants, six used the self‐report QoL‐AD. There was little or no difference between the reminiscence and control groups (random‐effects analysis; SMD 0.06, 95% CI ‐0.15 to 0.28; I2 = 56%; high quality evidence). The different settings (community versus care home) appeared to be responsible for the substantial level of inconsistency identified in this analysis. The findings for reminiscence groups at longer‐term follow‐up were detailed in the previous section. SettingThree studies including 193 participants living in care home settings were included in the meta‐analysis of self‐report QoL indices (Azcurra 2012; O'Shea 2014; Subramaniam 2013). The analysis suggested that there was probably an improvement in self‐reported QoL following a reminiscence intervention in care homes, but we could not be sure that this was large enough to be clinically important (fixed‐effect analysis; SMD 0.46, 95% CI 0.18 to 0.75; I2 = 0%; moderate quality evidence). The single care‐home study that reported longer‐term (six months) follow‐up, with 88 participants, also showed a probable improvement on the SR‐QoL (9.8 points, 95% CI 7.05 to 12.55; moderate quality evidence) (Azcurra 2012). Five studies with 867 participants included only community‐resident people with dementia (Amieva 2016; Charlesworth 2016; Särkämö 2013; Thorgrimsen 2002; Woods 2012a). All used the self‐report QoL‐AD. There was little or no difference between the reminiscence and control groups (fixed‐effect analysis; MD ‐0.57 points, 95% CI ‐1.37 to 0.22; I2 = 0%; high quality evidence). Four of these studies measured the effects of reminiscence on QoL of 786 participants living in the community at follow‐up time points of six to 21 months (Amieva 2016; Charlesworth 2016; Särkämö 2013; Woods 2012a). There was little or no difference between the reminiscence and control groups (QoL‐AD) (fixed‐effect analysis; MD 0.17 points, 95% CI ‐0.79 to 1.13; I2 = 0%; high quality evidence). Proxy ratingsThe above findings on QoL were based on self‐report measures. Five studies of reminiscence groups with 763 participants used proxy measures, where a family carer or member of care staff rated the person's QoL (Charlesworth 2016; O'Shea 2014; Särkämö 2013; Thorgrimsen 2002; Woods 2012a). All used the QoL‐AD proxy version. There was little or no difference in outcomes at the end of treatment (random‐effects analysis; MD 0.35 points, 95% CI ‐1.23 to 1.94; I2 = 45%; moderate quality evidence; Analysis 1.2). At longer‐term follow‐up of six to seven months postintervention, three studies with 505 participants, all community based and involving reminiscence groups, reported findings on the QoL‐AD proxy version (Charlesworth 2016; Särkämö 2013; Woods 2012a). There was little or no difference between the reminiscence and control groups (MD ‐0.15 points, 95% CI ‐1.14 to 0.83; I2 = 25%; high quality evidence; Analysis 1.18). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 2 Proxy rated quality of life post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 18 Proxy rated quality of life at follow‐up. Observed quality of lifeTwo studies used the WIB, an observational measure of QoL, which was completed during a minimum of six hours' observation of the person undertaking their usual activities (Azcurra 2012; Lai 2004). The studies included 154 care home participants, and there was probably little or no difference on WIB scores at end of treatment (MD 0.00 points, 95% CI ‐0.17 to 0.18; I2 = 0%; moderate quality evidence). At longer‐term follow‐up of six to 24 weeks' postintervention, due to the imprecision of the results and the development of inconsistency between the studies, we were unable to determine whether there was any effect of reminiscence on observed QoL (random‐effects analysis; MD ‐0.40 points, 95% CI ‐1.34 to 0.54; I2 = 93%; very low quality evidence; Analysis 1.19). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 19 Observed quality of life at follow‐up. Cognition(See Figure 5.) Forest plot of comparison: 1 Reminiscence therapy versus no treatment, outcome: 1.5 Cognition (overall) post‐treatment. For cognition, we analysed data from 14 studies involving 1219 people living with dementia, in which 679 received some form of reminiscence and 540 were assigned to control groups. Where studies used more than one measure of cognition, we used the most common or extensive assessment (for the AMI and AMI‐E this was the Personal Semantic Memory Sub‐scale (PSS)). There was a slight improvement in cognition immediately following a reminiscence intervention, but the effect was small and of uncertain clinical importance (change scores between reminiscence and control conditions: SMD 0.11, 95% CI 0.00 to 0.23; I2 = 9%; high quality evidence; Analysis 1.5). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 5 Cognition (overall) post‐treatment. The MMSE was the most widely used cognitive measure, used in nine studies involving 437 participants. A fixed‐effect analysis found an improvement following reminiscence compared to the control group (MD 1.87 points, 95% CI 0.54 to 3.20; I2 = 0%; high quality evidence). Nine studies measured the difference in cognition scores between reminiscence and control groups over a longer follow‐up period of six to 84 weeks postintervention. This involved 983 participants with 561 in the intervention groups and 422 in the control groups. There was little or no difference in outcome between groups (SMD 0.04, 95% CI ‐0.09 to 0.17; I2 = 3%; high quality evidence; Analysis 1.21). For the five studies reporting MMSE, there may have been an improvement at follow‐up of six to 36 weeks (MD 1.8 points, 95% CI ‐0.06 to 3.65; I2 = 0%; 282 participants; low quality evidence), with the quality rating reduced due to the relatively low sample size and imprecision. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 21 Cognition (overall) at follow‐up. ModalityThere was a probable slight improvement with individual reminiscence compared with the control group in five studies with 196 participants, but we could not be sure that this was large enough to be clinically important (SMD 0.32, 95% CI 0.04 to 0.61; I2 = 6%; moderate quality evidence). For individual reminiscence, two studies (both in care homes) with 83 participants reported results at six weeks' follow‐up. There may have been some benefit, but the results were so imprecise that we could not be certain of this, or whether any effect was large enough to be clinically important (SMD 0.35, 95% CI ‐0.08 to 0.79; I2 = 0%; low quality evidence). For the nine studies with 1023 participants of group reminiscence, there was little or no difference in cognition at the end of treatment between reminiscence and control groups (SMD 0.07, 95% CI ‐0.05 to 0.20; I2 = 0%; high quality evidence). For the six group reminiscence studies with 281 participants using the MMSE, there was a probable improvement in favour of reminiscence (MD 1.81 points, 95% CI 0.17 to 3.46; I2 = 0%; moderate quality evidence). For group reminiscence (all community‐based studies), there was little or no difference in cognition at longer‐term follow‐up of six to 84 weeks (SMD 0.01, 95% CI ‐0.12 to 0.14; I2 = 0%; 7 studies; 900 participants; high quality evidence). SettingSix studies in care homes, involving 230 participants, reported cognitive outcomes at end of treatment (Haight 2006; Ito 2007; Lai 2004; Morgan 2012; Subramaniam 2013; Van Bogaert 2016). There was a probable slight improvement in favour of the reminiscence intervention, but we could not be sure that this was large enough to be clinically important (SMD 0.29, 95% CI 0.03 to 0.56; I2 = 0%; moderate quality evidence). Eight studies with 989 participants were carried out in community settings. There was little or no difference in cognition apparent at the end of treatment between reminiscence and control groups (SMD 0.07, 95% CI ‐0.05 to 0.20; I2 = 8%; high quality evidence). All the community studies with long‐term follow‐up involved a group intervention and all those in care homes involved an individual intervention, and so these results have been detailed under 'Modality' above, with little or no difference for community/group studies, and uncertainty about possible benefit in care home/individual studies. Communication and interaction(See Figure 6.) Forest plot of comparison: 1 Reminiscence therapy versus no treatment, outcome: 1.7 Communication and interaction post‐treatment. Six studies with 249 participants, using a variety of different indicators of communication and interaction, were included in the end of treatment analysis (Azcurra 2012; Haight 2006; Lai 2004; Tadaka 2007 (AD); Tadaka 2007 (VD); Thorgrimsen 2002). (Note: in this analysis, negative scores indicated improved communication.) There may have been an improvement in communication and interaction following a reminiscence intervention, but, due to inconsistency between studies, we could not rule out a small or negligible effect (random‐effects analysis; SMD ‐0.51 points, 95% CI ‐0.97 to ‐0.05; I2 = 62%; low quality evidence; Analysis 1.7). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 7 Communication and interaction post‐treatment. Four of the six studies, with 204 participants, also reported data at six to 24 weeks' follow‐up (Azcurra 2012; Lai 2004; Tadaka 2007 (AD); Tadaka 2007 (VD)). There was probably an improvement in communication and interaction at longer‐term follow‐up after a reminiscence intervention, but we could not be sure that this was large enough to be clinically important (SMD ‐0.49 points, 95% CI ‐0.77 to ‐0.21; I2 = 0%; moderate quality evidence; Analysis 1.22). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 22 Communication and interaction at follow‐up. ModalityTwo studies using individual reminiscence reported end of treatment measures of communication and interaction (Haight 2006; Lai 2004). We could not be certain whether there was an improvement as the quality of the evidence was very low, due to imprecision and serious inconsistency (random‐effects analysis; SMD ‐0.74, 95% CI ‐2.38 to 0.89; I2 = 91%; very low quality evidence). Longer‐term follow‐up data were only available in one study of individual reminiscence (Lai 2004), with effects uncertain due to imprecision. Analysis of the four trials of group reminiscence, including 153 participants, indicated a probable slight improvement for participants receiving reminiscence compared with the control group at end of treatment, although we could not be certain of its clinical importance (SMD ‐0.39, 95% CI ‐0.71 to ‐0.06; I2 = 0%; moderate quality evidence) (Azcurra 2012; Tadaka 2007 (AD); Tadaka 2007 (VD); Thorgrimsen 2002). For group reminiscence, three studies with 138 participants reported data at six months' follow‐up (Azcurra 2012; Tadaka 2007 (AD); Tadaka 2007 (VD)). There was a probable improvement after this longer‐term follow‐up (SMD ‐0.63, 95% CI ‐0.97 to ‐0.29; I2 = 0%; moderate quality evidence). SettingThree studies, with 65 participants, were based in the community. There was a probable improvement on communication and interaction in favour of RT although we could not be certain it was clinically important (SMD ‐0.57, 95% CI ‐1.08 to ‐0.06; I2 = 0%; moderate quality evidence). At longer‐term follow‐up, only two studies, with 50 participants, took place in the community (Tadaka 2007 (AD); Tadaka 2007 (VD). There was a probable improvement in favour of RT, although we could not be certain it was clinically important (MOSES withdrawal subscale: MD ‐3.64 points, 95% CI ‐7.21 to ‐0.06; I2 = 0%; moderate quality evidence). Three studies with 184 participants took place in care homes. Here, we could not ascertain from our results whether there was an important effect on communication and interaction due to imprecision and unexplained variation in results between studies (random‐effects analysis; SMD ‐0.52, 95% CI ‐1.29 to 0.24; I2 = 83%; very low quality evidence). The two care home studies, with 154 participants, with longer‐term follow‐up of six to 24 weeks used the SES (Azcurra 2012; Lai 2004). There may have been an improvement; however, imprecision and inconsistency between the studies means we could not be certain of a clinically important effect (random‐effects analysis; MD ‐0.93 points, 95% CI ‐1.77 to ‐0.09; I2 = 41%; low quality evidence). Quality of relationshipThree studies, with 528 participants, included ratings by the person with dementia of his/her relationship with his/her family carer (Charlesworth 2016; Subramaniam 2013; Woods 2012a). All used the QCPR and reported results separately for its two subscales: warmth and absence of conflict. On both subscales, there was little or no difference between RT and control groups at the end of treatment (warmth: MD 0.16 points, 95% CI ‐0.53 to 0.84; I2 = 0%; high quality evidence; absence of conflict: MD ‐0.40 points, 95% CI ‐1.09 to 0.29; I2 = 15%; high quality evidence). Two of the studies, involving 415 participants, both community‐based and using reminiscence groups, reported seven months' follow‐up post‐intervention. Due to the imprecision of the results and inconsistency between the two studies, we were unable to determine whether there was any effect of reminiscence on warmth at follow‐up (random‐effects analysis; MD ‐0.09 points, 95% CI ‐1.82 to 1.63; I2 = 62%; low quality evidence). There was little or no difference in absence of conflict (MD ‐0.38 points, 95% CI ‐1.28 to 0.51; I2 = 11%; high quality evidence). Behaviour: functionSix studies, involving 1030 participants, assessed changes in the functional level of the person with dementia at the end of treatment (Amieva 2016; Azcurra 2012; Charlesworth 2016; Haight 2006; Lai 2004; Woods 2012a). In this analysis, a lower score indicated a more positive outcome. Due to imprecision and inconsistency between studies, we were uncertain whether RT improved function at the end of treatment (random‐effects analysis; SMD ‐0.24, 95% CI ‐0.69 to 0.21; I2 = 90%; very low quality evidence; Analysis 1.8). This uncertainty was present at longer‐term follow‐up (six to 84 weeks) in an analysis that involved five studies and 941 participants (random‐effects analysis; SMD ‐0.31, 95% CI ‐0.66 to 0.03; I2 = 83%; very low quality evidence; Analysis 1.24). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 8 Behaviour (function) post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 24 Behaviour (functional) at follow‐up. ModalityTwo studies, involving 96 participants, examined the effects of individual reminiscence on level of function (Haight 2006; Lai 2004). There was probably little or no difference in function between RT and control groups at the end of treatment (SMD ‐0.07, 95% CI ‐0.33 to 0.47; I2 = 0%; moderate quality evidence). Only the Lai 2004 study went on to assess participants at later follow‐up time points, with no effect evident at six weeks' post‐intervention. Four studies implementing a group reminiscence intervention reproted a relevant outcome at end of treatment in 934 participants and at follow‐up in 875 participants (Amieva 2016; Azcurra 2012; Charlesworth 2016; Woods 2012a). From baseline to end of treatment, the difference in change scores between the RT and control groups showed a probable slight benefit of RT (random‐effects analysis; SMD ‐0.40, 95% CI ‐0.99 to 0.20; I2 = 94%; moderate quality evidence). There was a similar slight improvement at longer‐term follow‐up of six to 21 months (random‐effects analysis; SMD ‐0.38, 95% CI ‐0.78 to 0.03; I2 = 87%; moderate quality evidence). In both cases, we could not be sure that the improvement noted was large enough to be clinically important; the high inconsistency in each analysis was clearly attributable to the inclusion of the Azcurra 2012 study, the only one of the four to be located in a care home setting, and which reported more positive results in this domain than the community‐based group studies. SettingThree large group studies, including 846 participants, provided data on the effects of RT on functioning of community residents (Amieva 2016; Charlesworth 2016; Woods 2012a). There was little or no difference in function at the end of treatment between groups (SMD 0.05, 95% CI ‐0.09 to 0.18; I2 = 0%; high quality evidence), with a slight improvement in favour of RT, of uncertain clinical importance, at longer‐term follow‐up (SMD ‐0.12, 95% CI ‐0.27 to 0.02; I2 = 0%; high quality evidence). Due to imprecision and inconsistency, we could not be certain of the effect of RT in care home settings (three studies with 184 participants; Azcurra 2012; Haight 2006; Lai 2004). This was true at the end of treatment (random‐effects analysis; SMD ‐0.53, 95% CI ‐1.87 to 0.80; I2 = 94%; very low quality evidence) and at longer‐term follow‐up (two studies with 154 participants; Azcurra 2012; Lai 2004) (random‐effects analysis; SMD ‐0.67, 95% CI ‐1.89 to 0.55; I2 = 92%; very low quality evidence). The inconsistency in results within these analyses was attributable to the more positive results reported by the one care home study using a group intervention (Azcurra 2012). Behaviour: agitation/irritabilityThree studies measured irritability and agitation using the MOSES irritability subscale (O'Shea 2014) and CMAI (Tadaka 2007 (AD); Tadaka 2007 (VD)). A lower score was indicative of improved agitation/irritability. The three studies included 359 participants, with 181 receiving an RT and 178 receiving control conditions, and all implemented a group reminiscence intervention. There was probably little or no difference in outcome between groups at the end of treatment (SMD 0.03, 95% CI ‐0.17 to 0.24; I2 = 0%; moderate quality evidence; Analysis 1.9). Two studies measured changes in behaviour scores again six months' post‐intervention (Tadaka 2007 (AD); Tadaka 2007 (VD)). There may have been a slight improvement, although we could not be certain of this, or of its clinical importance, due to imprecision (MD ‐1.52 points, 95% CI ‐4.07 to 1.03; I2 = 0%; low quality evidence; Analysis 1.25). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 9 Behaviour (agitation/irritability) post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 25 Behaviour (agitation/irritability) at follow‐up. All the studies were group studies, and in the absence of heterogeneity between studies, analyses by setting were not undertaken. Mood(See Figure 7.) Forest plot of comparison: 1 Reminiscence therapy versus no treatment, outcome: 1.10 Mood‐related outcomes (depression) post‐treatment. Ten studies included a mood scale administered at the end of treatment (Amieva 2016; Charlesworth 2016; Haight 2006; Morgan 2012; O'Shea 2014; Subramaniam 2013; Tadaka 2007 (AD); Tadaka 2007 (VD); Van Bogaert 2016; Woods 2012a). These included self‐report measures such as the HADS and the GDS, but four studies using the CSDD, where the researcher integrated reports from the carer and the person with dementia. In these analyses, negative scores indicated improved mood. For depression, the 10 studies included 973 participants. There was little or no difference in depression between groups evident at the end of treatment (SMD ‐0.03, 95% CI ‐0.15 to 0.10; I2 = 32%; high quality evidence; Analysis 1.10). At longer‐term follow‐up (six to 84 weeks), six studies, including 747 participants, reported measures of depressed mood. We could not be certain of the effects of RT at follow‐up, as the results were consistent with improvement or with little or no effect, and there was inconsistency between studies attributable to the reminiscence modality (random‐effects analysis; SMD ‐0.16, 95% CI ‐0.43 to 0.11; I2 = 55%; moderate quality evidence; Analysis 1.26). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 10 Mood‐related outcomes (depression) post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 26 Mood‐related outcomes (depression) at follow‐up. Two large community‐based studies of group reminiscence, including 436 participants, analysed anxiety (Charlesworth 2016; Woods 2012a). There was little or no difference in anxiety between groups at the end of treatment (SMD ‐0.03, 95% CI ‐0.22 to 0.16; I2 = 0%; high quality evidence; Analysis 1.11), and there was probably little or no difference in anxiety at seven months' follow‐up (SMD 0.01, 95% CI ‐0.20 to 0.21; I2 = 0%; moderate quality evidence; 391 participants; Analysis 1.27). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 11 Mood‐related outcomes (anxiety) post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 27 Mood‐related outcomes (anxiety) at follow‐up. One study with 326 participants evaluated apathy, using a carer‐rated Apathy Index (Amieva 2016). There was probably little or no difference in apathy between groups at the end of treatment assessment or at 21 months' follow‐up. ModalityThe four studies using an individual reminiscence approach included 131 participants. There was probably a slight effect on depressed mood in favour of individual RT, although we could not be sure of its clinical importance (SMD ‐0.41, 95% CI ‐0.76 to ‐0.06; I2 = 0%; moderate quality evidence). The single study with an individual approach that included a longer‐term follow‐up (six weeks) showed a probable benefit, but the sample size (17 participants) was very small (Morgan 2012). Six studies with 842 participants used a group approach. There was little or no difference between group RT and controls (SMD 0.03, 95% CI ‐0.10 to 0.17; I2 = 27%; high quality evidence). At longer‐term follow‐up of six to 21 months, five studies of group RT reported measures of depressed mood, but all were community based, so the results were confounded with the setting. There was little or no difference related to the RT (SMD ‐0.04, 95% CI ‐0.19 to 0.11; I2 = 0%; high quality evidence; 730 participants). SettingFive studies with 187 participants were based in care homes. There was probably a small benefit of RT, but we could not rule out little or no effect and could not be sure of the clinical importance of any effect (SMD ‐0.19, 95% CI ‐0.48 to 0.10; I2 = 30%; moderate quality evidence). The five community‐based studies, all involving group interventions, included 786 participants and showed little or no effect of RT (SMD 0.01, 95% CI ‐0.13 to 0.16; I2 = 31%; high quality evidence). The results for longer‐term follow‐up were discussed in the 'Modality' section above, with all the community studies being group studies, and the single care home study followed up involving individual reminiscence. Outcomes for the carerFor all carer outcomes, lower scores indicated a more positive outcome. Stress related to caringSeven studies used measures such as the Relative Stress Scale (RSS) and ZBI that evaluated the carer's stress directly related to aspects of caring (Amieva 2016; Azcurra 2012; Charlesworth 2016; O'Shea 2014; Särkämö 2013; Thorgrimsen 2002; Woods 2012a). In six of the studies, the carer was a family member or friend, but in the O'Shea 2014 study, the carer was a healthcare assistant or nurse. At end of treatment, these studies involved 1155 participants. Overall, there was probably little or no difference in carer stress related to the reminiscence intervention (random‐effects analysis; SMD ‐0.03, 95% CI ‐0.21 to 0.14; I2 = 43%; moderate quality evidence; Analysis 1.12). There appeared to be some inconsistency between studies, related to the different settings. Excluding the O'Shea 2014 study, so that the 965 participants were all family or friend carers made little difference to the overall results (random‐effects analysis; SMD ‐0.08, 95% CI ‐0.32 to 0.16; I2 = 59%; high quality evidence). The inclusion of a single care home study, which reported much more positive findings, was responsible for the observed inconsistency (Azcurra 2012). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 12 Carer outcomes (stress related to caring) post‐treatment. Five studies, involving 895 participants, went on to measure carer stress at follow‐up of six to 21 months (Amieva 2016; Azcurra 2012; Charlesworth 2016; Särkämö 2013; Woods 2012a). The results were again inconsistent between studies (due to the inclusion of the single care home study) and the result of the meta‐analysis was imprecise being compatible with either improvement or a small or no effect (random‐effects analysis; SMD ‐0.19, 95% CI ‐0.54 to 0.16; I2 = 82%; moderate quality evidence; Analysis 1.28). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 28 Carer outcomes (stress related to caring) at follow‐up. ModalityAll the seven studies that measured stress related to caring involved group reminiscence (Amieva 2016; Azcurra 2012; Charlesworth 2016; O'Shea 2014; Särkämö 2013; Thorgrimsen 2002; Woods 2012a). However, an additional aspect of modality that should be considered in relation to carer outcomes relates to whether the family carer was actively involved in the reminiscence group. This joint reminiscence was a key feature of the Charlesworth 2016; Särkämö 2013; Thorgrimsen 2002 and Woods 2012a studies, which included 551 participants. There was little or no difference in carer stress between the reminiscence intervention and control conditions at end of treatment in these studies (SMD 0.04, 95% CI ‐0.13 to 0.21; I2 = 16%; high quality evidence) or at longer‐term follow‐up of six to seven months (SMD ‐0.04, 95% CI ‐0.22 to 0.15; I2 = 0%; high quality evidence; 3 studies; 481 participants). In contrast, only one study including 88 participants evaluated family carer stress when family carers were not extensively involved in the RT (Azcurra 2012). The study used the ZBI and found that there was probably a benefit to carers at the end of treatment (MD ‐4.90 points, 95% CI ‐8.20 to ‐1.60; moderate quality evidence) and at six months' follow‐up (MD ‐7.90 points, 95% CI ‐10.97 to ‐4.83; moderate quality evidence). SettingFive studies, including 877 participants, were community‐based (Amieva 2016; Charlesworth 2016; Särkämö 2013; Thorgrimsen 2002; Woods 2012a). There was little or no difference in carer stress between groups at end of treatment (SMD 0.05, 95% CI ‐0.08 to 0.19; I2 = 0%; high quality evidence) or at longer‐term follow‐up of six to 21 months (SMD 0.02, 95% CI ‐0.12 to 0.16; I2 = 0%; high quality evidence; 4 studies; 807 participants). There were two care home studies, both using the ZBI (Azcurra 2012; O'Shea 2014). The Azcurra 2012 study, which involved family carers, reported probable benefit at both end of treatment and longer‐term follow‐up, but, when combined with the O'Shea 2014 study, end of treatment data on staff carers, we could not be certain of any benefits due to inconsistency between the studies and imprecision (random‐effects analysis; MD ‐1.48 points, 95% CI ‐5.43 to 2.47; I2 = 70%; very low quality evidence; 278 participants). Mood: depression and anxietyTwo large community‐based joint reminiscence group studies with 517 participants used the HADS to evaluate changes in anxiety and depressed mood following carers' participation in joint reminiscence groups with people with dementia (Charlesworth 2016; Woods 2012a). There was little or no difference between groups on the HADS Anxiety subscale at the end of treatment (MD 0.06 points, 95% CI ‐0.54 to 0.66; I2 = 0%; high quality evidence; Analysis 1.14). At seven months' follow‐up, there was probably a slight advantage for the control participants, but we could not be certain of the clinical implications of this result, which was also consistent with little or no difference (MD 0.56 points, 95% CI ‐0.17 to 1.30; I2 = 0%; moderate quality evidence; 464 participants; Analysis 1.30). There was little or no difference between reminiscence and control conditions for the HADS Depression subscale at the end of treatment (MD ‐0.08 points, 95% CI ‐0.59 to 0.44; I2 = 0%; high quality evidence; Analysis 1.13) and at seven months' follow‐up (MD ‐0.05 points, 95% CI ‐0.71 to 0.60; I2 = 0%; high quality evidence; Analysis 1.29). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 13 Carer outcomes (depression) post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 14 Carer outcomes (anxiety) post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 29 Carer outcomes (depression) at follow‐up. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 30 Carer outcomes (anxiety) at follow‐up. Well‐being and quality of lifeFour community‐based joint reminiscence group studies, including 530 participants, evaluated aspects of carer psychological well‐being (Charlesworth 2016; Särkämö 2013; Thorgrimsen 2002; Woods 2012a). Outcome scales included the GHQ‐12, GHQ‐28 and SF‐12 Mental component. There was little or no difference in carer well‐being between groups at end of treatment (SMD ‐0.04, 95% CI ‐0.22 to 0.13; I2 = 1%; high quality evidence; Analysis 1.15). Three studies provided longer‐term follow‐up data after six to seven months, and there was little or no difference in carer well‐being (SMD 0.01, 95% CI ‐0.18 to 0.19; I2 = 0%; high quality evidence; 467 participants; Analysis 1.31) (Charlesworth 2016; Särkämö 2013; Woods 2012a). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 15 Carer outcomes (quality of life) post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 31 Carer outcomes (quality of life) at follow‐up. Quality of caring relationshipThree studies, including up to 528 participants, evaluated the quality of the relationship between the carer and the person with dementia (as rated by the carer), all using the QCPR with two subscales: warmth and absence of conflict (Charlesworth 2016; Subramaniam 2013; Woods 2012a). There was little or no difference related to RT on the warmth subscale at the end of treatment (MD ‐0.01 points, 95% CI ‐0.77 to 0.76; I2 = 0%; high quality evidence) or (for the Charlesworth 2016 and Woods 2012a studies) after seven months' follow‐up (MD ‐0.66 points, 95% CI ‐1.59 to 0.27; I2 = 0%; high quality evidence). Similarly, there was little or no difference on the absence of conflict subscale at end of treatment (MD ‐0.26 points, 95% CI ‐1.01 to 0.48; I2 = 0%; high quality evidence) or after longer‐term follow‐up (MD ‐0.37 points, 95% CI ‐1.23 to 0.50; I2 = 0%; high quality evidence). Adverse outcomesThe only outcome identified that probably favoured control participants was carer anxiety at seven months' follow‐up, from an analysis involving two large community studies that involved family carers along with people with dementia in reminiscence groups. The estimated MD was small enough to be of uncertain clinical importance and the evidence was of moderate quality, downgraded due to imprecision. These two studies also reported a few incidences of specific adverse outcomes. The Charlesworth 2016 study recorded 159 'serious adverse events' during the trial, with three of these attributable to the RYCT intervention. Specific details were not given, though it reported that none of these three events led to withdrawal. The Woods 2012a study recorded one adverse event linked to participation in the trial. One participant became upset in one of the intervention sessions relating to marriage. There was a detailed protocol for dealing with distressing events that was implemented. While adverse events are regrettable, it is important to view them in context of the total number of participants and intervention sessions. DiscussionSummary of main resultsThere has been a welcome increase in the volume of research on reminiscence in dementia care (and an improvement in its quality) since this review was last updated. It has now been possible to include large‐scale multicentre RCTs, using clearly defined interventions and protocols. It has also been possible to exclude studies where the risk of bias was rated as too high, without detracting greatly from the volume of research considered. For several outcomes, meta‐analyses included 800 or more participants. For the first time, it was possible to undertake analyses taking into account different modalities of reminiscence work and different contexts. Individual and group reminiscence work can now be considered separately for several outcomes, and community studies distinguished from those carried out in care homes. The primary finding of the review was that reminiscence work was not associated consistently with improved well‐being and QoL for people with dementia assigned to receive it in research studies. Although its clinical importance was uncertain, in care homes, but not in community settings, there was a probable benefit on QoL measures immediately following the reminiscence intervention. This finding arose from a meta‐analysis of three studies, from different countries, involving 193 people with dementia. Notably, in four of the five community studies in this analysis (and none of the care home studies), the intervention involved joint group sessions, where people with dementia and their family carers participated together. The extent to which reminiscence work would be predicted to improve cognitive functioning is debatable, but this review provides evidence (across 14 studies involving 1219 people with dementia) of a small benefit on cognitive tests evident immediately following the reminiscence work, but not sustained after a longer follow‐up period. The analyses separating individual and group reminiscence work indicated probable slight benefits in cognition related to individual work. There was a probable slight benefit to cognition in care homes but not the community. The overall effect size for cognition at the end of treatment (SMD) was 0.11 (95% CI 0.00 to 0.23); the comparable SMD from the Cochrane Review of cognitive stimulation (Woods 2012b) was 0.41 (95% CI 0.25 to 0.57). However, a direct comparison of the subset of studies using the MMSE in the two reviews indicated an MD of 1.74 points (95% CI 1.13 to 2.36), from 10 studies of cognitive stimulation involving 600 participants, compared with an MD of 1.87 points (95% CI 0.54 to 3.20) for nine studies of RT involving 437 participants. This suggests the effects may be comparable on the MMSE between the two types of interventions, but with a wider CI for the reminiscence result. The quality of evidence relating to the communication and interaction outcome was lower, but there was probably a benefit of RT at longer‐term follow‐up, albeit of uncertain clinical importance. The number of studies including a relevant outcome measure was smaller (six at end of treatment, four at follow‐up, with 200 or more participants in each case), and the large studies of joint (with carer) reminiscence work were among those without a relevant outcome measure in this domain. Here, a probable effect was evident for community‐based studies at end of treatment and follow‐up, but was even less certain in the care home context. Group reminiscence was associated with a probable slight benefit in communication immediately and a benefit within the clinically important range at follow‐up, whereas (in smaller studies) there was considerable uncertainty in the results for individual reminiscence work. Despite a body of evidence for the effects of reminiscence on depressed mood in older people without dementia (e.g. Bohlmeijer 2003; Pinquart 2007), only individual reminiscence work was associated with a probable improvement in mood for people with dementia in this review, and the size of the effect (SMD ‐0.41) was relatively small and of uncertain clinical importance. There were no indications of benefits associated with reminiscence work in relation to the other outcomes examined for the person with dementia. These included the person's level of function, extent of irritability and agitation, and their own rating of the quality of relationship with their family carer. Despite the inclusion of several large studies of joint reminiscence work, where family carers were fully involved in the reminiscence sessions, we identified no benefits for family carers in relation to reduced stress related to caring, well‐being and QoL, carer mood or the carer's rating of the quality of their relationship with the person with dementia. The only exception to this was a single care home study, with 88 participants, in which family carers probably experienced less stress after their relative had been involved in reminiscence groups, both immediately after treatment and at six months' follow‐up. Interestingly, this was the only study to examine family carer outcomes that did not have a focus on joint reminiscence work. There were some suggestions from the REMCARE (REMiniscence groups for people with dementia and their family CAREgivers) trial (Woods 2012a) of negative effects on carer anxiety, and this was evident to an extent in the analyses combining data from several studies of joint reminiscence work, where there was slightly higher carer anxiety (a difference of uncertain clinical importance) at the seven months' follow‐up assessment. One qualitative study explored potential factors in increased anxiety among carers taking part in joint reminiscence groups (Melunsky 2015). It identified issues such as the carer feeling disappointed when improvements in the group setting were not evident at home; the carer seeing people with more advanced dementia, resulting in increased fears for what the future might hold; and increased guilt from not being able to put into practice skills learned in the groups. These negative aspects were in the context of many positive experiences that carers reported from participation in the groups for themselves and the person with dementia. Overall completeness and applicability of evidenceAlthough there is now a sufficient body of evidence to enable us to draw conclusions regarding reminiscence work in general, it remains difficult to consider fully different types of reminiscence work. For example, studies of individual reminiscence work have tended to be small‐scale and carried out in care homes, so we could not be certain of any difference in outcomes between individual and group approaches. Related to this, we were unable to draw a distinction in our analyses between simple and integrative reminiscence work. Although some studies have followed a very clear, published treatment protocol, reporting of details of interventions in other studies has been less complete, with even the distinction between individual and group reminiscence not always immediately apparent. Little evidence has emerged regarding the characteristics of people with dementia that might be associated with better outcomes, with the exception of the suggestion that reminiscence has a stronger effect on QoL in a care home context, as opposed to community settings. There clearly are differences between studies in the extent (and direction of changes) demonstrated by the high levels of heterogeneity evident in several analyses. However, many of these differences are yet to be explained. Some studies included only people with AD; others only recruited people with VD; others included any form of dementia. No clear differences in outcomes related to dementia type emerged from the analyses undertaken, and similarly there were few indications of the effects of dementia severity. It is unlikely that there is a simple 'dose' related effect, in that the studies offering the greatest exposure to reminiscence activities were among those with the least positive findings (Amieva 2016; Charlesworth 2016; Woods 2012a). However, within studies a 'dose' effect may have operated. It is clear that in community settings, a significant proportion of people randomised to receive a reminiscence intervention did not engage with the groups. For example, in Woods 2012a, 11% of participants did not attend a single reminiscence session, with over 25% attending three sessions or fewer. An even larger proportion of participants in the Charlesworth 2016 study (43%) did not attend any reminiscence sessions. In line with our protocol, we included the ITT results in our analyses in this review. While it is important to know that these groups may not, for a variety of reasons, be taken up by all people with dementia and their carers, their results must underestimate any actual direct effects of reminiscence. For example, in a compliance analysis, Woods 2012a showed an improvement in cognitive function (AMI‐E PSS) at the end of treatment and improved QoL (European Quality of Life 5 Dimensions; EQ‐5D) and quality of relationship (QCPR) at longer‐term follow‐up, but accompanied by an increase in carer stress (RSS). In contrast, Charlesworth 2016 reported no relationship between attendance and outcomes. Quality of the evidenceThere has been an overall significant improvement in the quality of included studies since the previous version of this review was undertaken. We are now able to include large‐scale studies, overseen by accredited clinical trials units, with quality assurance procedures and well‐developed remote randomisation procedures. However, more generally, under‐reporting of details of trials meant that a number of authors had to be contacted for additional information regarding, for example, randomisation and allocation, and several studies were excluded because of their risk of bias. Some risks of bias arise from the nature of psychosocial interventions such as RT. Participants and carers will be aware of the intervention being received, and, in general single‐blinding is the aim, with assessors being blind to treatment allocation. However, ratings completed by, for example, staff in care homes, may not be blinded, and the blinding of assessors may be compromised by participants and carers providing indications a treatment intervention has been received. Studies such as Woods 2012a asked assessors to indicate which group the participant was in, and their degree of certainty of their judgement so that the extent of bias could be estimated. Expectations of benefit from participation or resentment at not being allocated to the active treatment may occur, and may produce some additional bias. Treatment expectations may be seen in the context of a pragmatic trial as part of the overall 'treatment package,' of course. Potential biases in the review processOur search strategy was as comprehensive as possible, and we consulted with experts in the field to identify any further studies. Two review authors (LOP and EF) independently conducted selection of studies, data extraction and risk of bias assessments, and disagreements resolved by contacting authors and consultation with other members of the review author team. The present review included all outcomes detailed in the protocol, irrespective of whether or not the results identified improvements. It must be acknowledged that the included studies could represent a biased sample of the studies undertaken worldwide on RT. It may be the case that trials that are not 'successful' (i.e. do not produce the expected positive findings) are less likely to be published. This may be especially the case with smaller trials. The welcome trend to preregistration of trials, and the publication of trial protocols, makes this less likely to occur in the future in relation to larger, well‐funded trials. The meta‐analyses here have been influenced strongly by larger trials, several of which did not report any positive findings (e.g. Charlesworth 2016; Woods 2012a), but these were both of a group approach, in community settings. Our care home and individual reminiscence findings could perhaps have been more influenced by publication bias. A funnel plot of cognition at the end of treatment showed some asymmetry (Figure 8), but this was largely driven by smaller/lower quality community studies having positive findings, with care home studies showing a symmetrical pattern. For most of our outcomes, there are too few included studies for meaningful funnel plots to be plotted. Funnel plot of comparison: 1 Reminiscence therapy versus no treatment, outcome: 1.5 Cognition (overall) post‐treatment. ADAS‐Cog: Alzheimer’s Disease Assessment Scale for Cognition; AMI‐PSS: Autobiographical Memory Interview ‐ Perceived Stress Scale; AMI‐E‐PSS: Autobiographical Memory Interview Extended Version ‐ Perceived Stress Scale; MMSE: Mini‐Mental State Examination. Agreements and disagreements with other studies or reviewsWe identified five reviews that overlap with this one. Cotelli 2012 included seven RCTs, with 218 participants, three of which were included in the current review. They identified some benefits for mood and cognitive function but pointed out that the number of trials 'remains very small and their quality is often poor' (two were excluded from this review on the basis of risk of bias). This review appeared to have predated the recent improvement in quality and size of trials. Subramaniam 2012 focused on individual reminiscence work, identifying five RCTs, three of which were included in the current review. They concluded that there was a consistent pattern emerging, with those studies offering 'individual reminiscence work that includes a life review process, uses specific memory triggers and results in the production of a life story book' having positive psychosocial outcomes for people with dementia. In contrast, where reminiscence was more general, evidence for efficacy was not apparent. Unfortunately, there are still insufficient studies of integrative reminiscence work to confirm this early conclusion. Kwon 2013 reported a meta‐analysis including 10 studies. The studies included are not referenced, so comparisons were difficult. They conclude that reminiscence had a positive effect on cognition, depression and QoL, all with large effect sizes, but not on problem behaviour. Testad 2014 reported a broader review relating to people with dementia in care homes, with RT included as one of several psychosocial interventions. They included six studies involving RT, most of which did not meet the inclusion criteria for the current review (e.g. three were not RCTs). The authors concluded that reminiscence was associated with improved mood, but there was no consistent evidence regarding other outcomes. Huang 2015 included 12 studies, with 1325 participants. Cognition and depressed mood were the main outcomes studied, with nine studies contributing to meta‐analyses in each case. As with the current review, they identified a small effect size for cognition (SMD 0.18, 95% CI 0.05 to 0.30) but unlike the current review, there was a moderate‐sized effect for depressed mood (SMD ‐0.48, 95% CI ‐0.70 to ‐0.28). There was evidence that the effect on mood was greater in care home settings than in the community, which is in accordance with our results. Notably the community studies included in the Huang 2015 review were all included in this review, but there were differences in the care home studies included, partly due to different exclusion criteria, but also because they were able to include studies published in Chinese. In general, the current review has adopted stricter quality standards than other reviews, and identified considerably more studies for inclusion, across different modalities and settings. Authors' conclusionsImplications for practiceWhilst this updated review has shown that reminiscence therapy (RT) can improve outcomes for people with dementia, its effects are inconsistent, often small in size and can differ considerably across settings and modalities. The outcomes for which some benefit has been identified are cognitive function, communication/interaction, quality of life (QoL) and mood. However, the effects are not consistent across different types of reminiscence work (group or individual, with or without family carer involvement), or across different contexts (care home or community), particularly where QoL is the outcome. The evidence relating to QoL is most promising in care homes; that relating to mood is most promising for individual RT. RT can now be viewed alongside cognitive stimulation as an ecopsychosocial intervention with a credible evidence‐base. Individual and group approaches have some support, although the two large, well‐conducted UK studies of joint reminiscence group work involving family members alongside people with dementia have been the studies showing the smallest effects. Individual work has the potential benefit of resulting in some form of life story book, which provides a platform to enhance person‐centred care. However, to date it has not proven clearly superior to group work, which may have added value in terms of enhancing interaction and communication. The lack of participation in the two UK studies of joint reminiscence work suggests that consideration should be given to offering it as one of a number of approaches, as participation does not appear to be valued by a significant number of people with dementia and carers. Where it is offered, benefits beyond the 'in the moment' enjoyment of a shared social group experience, should not be anticipated as general outcomes. The diversity of approaches to reminiscence seen in the various studies suggests that there is a need for manuals and training to be developed so that approaches can be more readily shared, and common approaches developed, for both individual and group work. It is essential that the different functions of reminiscence and the different types of reminiscence work are recognised, to aid sharing of good practice and understanding of the training, support and resources needed for implementation. Implications for researchThe research agenda in relation to reminiscence work now needs to address some of the discrepancies and uncertainties highlighted by this review, and more fully reflect and identify the differences in function and types of reminiscence work. A large scale randomised controlled trial (RCT) of individual, integrative reminiscence work, producing a conventional or digital life story book, would demonstrate whether the promising results from small studies could be replicated on a larger platform, with greater attention to the detail of randomisation and allocation concealment. Such a study should include enough people living with dementia in care home and community settings, and with a range of severities of impairment, so that more fine‐grained conclusions may be drawn. Research is also needed on the extent to which reminiscence work can drive person‐centred care, so that the person's biography becomes a rich resource for planning and action. There has been increasing interest in digital reminiscence work (e.g. Subramaniam 2010; Subramaniam 2016), but to date there have been no studies meeting the criteria for inclusion in the current review. This is clearly an area where more research is justified, in developing the intervention and then delineating its effects. The research to date has emphasised changes beyond the group, on measures carried out before and after a set number of reminiscence sessions. More emphasis on the experience of people with dementia (and carers) within the reminiscence session may be helpful. Is each session an enjoyable experience in itself, even if the lasting benefits are more elusive? Brooker 2000 used an observational method, Dementia Care Mapping, to demonstrate that people with dementia showed greater well‐being when participating in simple reminiscence groups than when undertaking other activities, and it would be helpful to take this 'in the moment' evaluation approach further. Finally, in view of the significant number of people not taking up reminiscence interventions, research would be helpful delineating who does take it up and why, and what type of approach is beneficial for which people, so there can be better tailoring of interventions to individuals. What's new
HistoryProtocol first published: Issue 2, 1998
AcknowledgementsThe authors wish to thank Sue Marcus, Jenny McCleery and Anna Noel‐Storr of the Cochrane Dementia and Cognitive Improvement Group for their invaluable assistance. They are also grateful to the authors who provided additional data or clarification regarding their studies. AppendicesAppendix 1. Update searches: July 2011, October 2014, April 2015, April 2016, April 2017
NotesNew search for studies and content updated (conclusions changed) Data and analysesComparison 1Reminiscence therapy versus no treatment
Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 3 Observed quality of life (post‐treatment). Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 4 Cognition post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 6 Quality of caring relationship post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 16 Carer outcomes (quality of caring relationship) post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 20 Cognition follow‐up. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 23 Quality of caring relationship at follow‐up. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 32 Carer outcomes (quality of caring relationship) at follow‐up. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 33 Mood‐related outcomes (apathy) post‐treatment. Analysis Comparison 1 Reminiscence therapy versus no treatment, Outcome 34 Mood‐related outcomes (apathy) at follow‐up (community). Characteristics of studiesCharacteristics of included studies [ordered by study ID]
Characteristics of excluded studies [ordered by study ID]
Characteristics of ongoing studies [ordered by study ID]
Differences between protocol and reviewCurrent review includes updated use of 'Risk of bias' tool, use of GRADE approach, inclusion of 'Summary of findings' tables, methods to deal with data from cluster randomised controlled trials and subgroup analyses. In this review, unlike the previous versions, we were able to exclude studies from meta‐analyses on the grounds of quality. Contributions of authorsOriginal version and first update:
Update 2005:
Update 2017:
Sources of supportInternal sources
External sources
Declarations of interestBW: None known LOP: None known EMF: None known AES: None known MO: None known ReferencesReferences to studies included in this reviewAkanuma 2011 {published data only}
Amieva 2016 {published data only}
Azcurra 2012 {published and unpublished data}
Baines 1987 {published data only}
Charlesworth 2016 {published and unpublished data}
Goldwasser 1987 {published data only}
Gonzalez 2015 {published data only}
Haight 2006 {published and unpublished data}
Hsieh 2010 {published data only (unpublished sought but not used)}
Ito 2007 {published data only}
Lai 2004 {published and unpublished data}
Melendez 2015 {published and unpublished data}
Morgan 2012 {published data only}
O'Shea 2014 {published and unpublished data}
Särkämö 2013 {published and unpublished data}
Subramaniam 2013 {published data only}
Tadaka 2007 (AD) {published data only}
Tadaka 2007 (VD) {published data only}
Thorgrimsen 2002 {published data only}
Van Bogaert 2016 {published data only}
Woods 2012a {published and unpublished data}
Yamagami 2012 {published data only (unpublished sought but not used)}
References to studies excluded from this reviewAfonso 2009 {published data only}
Akhoondzadeh 2014 {published data only}
Allen 2014 {published data only}
Asiret 2016 {published data only}
Baillon 2004 {published data only}
Baillon 2005 {published data only}
Barban 2016 {published data only}
Bogaert 2013 {published data only}
Bohlmeijer 2008 {published data only}
Brooker 2000 {published data only}
Burckhardt 1987 {published data only}
Chao 2006 {published data only}
Chenoweth 2009 {published data only}
Chiang 2010 {published data only}
Choy 2016 {published data only}
Chueh 2014 {published data only}
Chung 2009 {published data only}
Crook 2016 {published data only}
Curto Prieto 2015 {published data only}
Eritz 2016 {published data only}
Gudex 2010 {published data only}
Haight 2003 {published data only}
Haslam 2010 {published and unpublished data}
Haslam 2014 {published data only}
Head 1990 {published data only}
Hilgeman 2014 {published data only}
Hsu 2009 {published data only}
Hutson 2014 {published data only}
Jo 2015 {published data only}
Lalanne 2015 {published data only}
Lancioni 2014 {published data only}
Lin 2011 {published data only}
Liu 2007 {published data only}
Lopes 2016 {published data only}
MacKinlay 2009 {published data only}
Mackinlay 2010 {published data only}
McKee 2003 {published data only}
McMurdo 2000 {published data only}
Melendez‐Moral 2013 {published data only}
Morris 2015 {published data only}
Nakamae 2014 {published and unpublished data}
Nakatsuka 2015 {published data only}
Orten 1989 {published data only}
Politis 2004 {published data only}
Rattenbury 1989 {published data only}
Rawtaer 2015 {published data only}
Sabir 2016 {published data only}
Serrano 2004 {published data only}
Stinson 2006 {published data only}
Tadaka 2004 {published data only}
Tanaka 2017 {published data only}
Thornton 1987 {published data only}
Tolson 2012 {published data only}
Van Dijk 2012 {published data only}
Wang 2004 {published data only}
Wang 2007 {published data only}
Wang 2009 {published data only}
Wingbermuehle 2014 {published data only}
Wu 2016 {published data only}
Yamagami 2007 {published data only}
Yasuda 2009 {published data only}
Yousefi 2015 {published data only}
Zauszniewski 2004 {published data only}
References to ongoing studiesDwolatzky 2014 {published data only}
Additional referencesAkanuma 2006
Altman 2005
Bohlmeijer 2003
Bohlmeijer 2007
Bruce 1998
Bruce 1999
Butler 1963
Cotelli 2012
DSM‐IV
Erikson 1950
Folstein 1975
Gerben 2010
Guyatt 2011
Haber 2006
Haight 1992
Hellen 1998
Help the Aged 1981
Higgins 2011
Huang 2015
Hughes 1982
Kiernat 1979
Kwon 2013
Melunsky 2015
Mohs 2000
Morris 1994
Norris 1986
Pinquart 2007
Pinquart 2012
Pot 2010
RevMan 2014 [Computer program]
Romaniuk 1981
Ros 2016
Schweitzer 2008
Soltys 1994
Subramaniam 2010
Subramaniam 2012
Subramaniam 2016
Tadaka 2007
Testad 2014
Woods 2012b
Woods 2016
Zhang 2015
References to other published versions of this reviewWoods 2005
Articles from The Cochrane Database of Systematic Reviews are provided here courtesy of Wiley Which clinical manifestation may present in a patient with dementia?Common signs and symptoms include acting out one's dreams in sleep, seeing things that aren't there (visual hallucinations), and problems with focus and attention. Other signs include uncoordinated or slow movement, tremors, and rigidity (parkinsonism). Frontotemporal dementia.
Which therapeutic strategy provides dementia patients with the opportunity to participate in different activities that may engage sight hearing taste smell and touch?Reminiscence therapy is a treatment that uses all the senses — sight, touch, taste, smell and sound — to help individuals with dementia remember events, people and places from their past lives. As part of the therapy, care partners may use objects in various activities to help individuals with recall of memories.
Which condition can be inferred in a patient who complains of involuntary release of urine while laughing sneezing and coughing?Stress incontinence occurs when urine leaks as pressure is put on the bladder, such as during exercise, coughing, sneezing, laughing, or lifting heavy objects.
Which finding will the nurse document as a normal aging process quizlet?Which patient's finding will the nurse document as a normal aging process? Loss of skin elasticity is a normal aging process because of loss of elastic tissue under the skin. Therefore, the nurse will document patient C's finding as a normal aging process.
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