- Study protocol
- Open Access
German adaptation of the Resources for Enhancing Alzheimer’s Caregiver Health II: study protocol of a single-centred, randomised controlled trial
© Heinrich et al.; licensee BioMed Central Ltd. 2014
- Received: 23 January 2014
- Accepted: 10 February 2014
- Published: 12 February 2014
Caring for a family member with dementia is extremely stressful, and contributes to psychiatric and physical illness among caregivers. Therefore, a comprehensive programme called Resources for Enhancing Alzheimer’s Caregiver Health II (REACH II) was developed in the United States to enhance the health of Alzheimer’s caregivers. REACH II causes a clear reduction of the stress and burdens faced by informal caregivers at home. The aim of this protocol is to adapt, apply, and evaluate this proven intervention programme in a German-speaking area for the first time. This newly adapted intervention is called Deutsche Adaption der Resources for Enhancing Alzheimer’s Caregiver Health (DeREACH).
A total of 138 informal caregivers at home are recruited in a single-centred, randomised controlled trial. The intervention (DeREACH) consists of nine home visits and three telephone contacts over six months, all of which focus on safety, psychological well-being and self-care, social support, problem behaviour and preventive health-related behaviours. A complex intervention assessment on effectiveness will be adopted when the primary outcome – namely, the reduction of caregiver burden – and other secondary outcomes, including changes with regard to anxiety and depression, somatisation, health-related quality of life, and perceived social support, are measured at baseline, as well as immediately and three months after the intervention. The change from baseline to post-intervention assessment with regard to the primary outcome will be compared between treatment and control group using t-tests for independent samples.
It is anticipated that this study will show that DeREACH effectively reduces caregiver burden and therefore works under the conditions of a local German health-care system. If successful, this programme will provide an effective intervention programme in the German-speaking area to identify and develop the personal capabilities of informal caregivers to cope with the burdens of caring for people with dementia.
- REACH II
- Informal caregivers
Caring for people with dementia is connected with enormous personal responsibilities and restrictions; therefore, family caregivers of people with dementia often feel more burdened and stressed than caregivers of older people with physical impairments . Due to this high stress level, there is a higher risk of these informal caregivers becoming physically or mentally diseased . For these caregivers, the conditions of experiencing stress and burden are complex , and the non-cognitive symptoms of dementia such as psychotic symptoms, depression, and challenging behaviour seem to play a significant role in this process .
American scientists created a wide-ranging programme regarding the development of effective interventions to support informal caregivers of people with dementia. In this programme, known as Resources for Enhancing Alzheimer’s Caregiver Health (REACH I) [5, 6], the researchers tested, evaluated, and compared various single- and multi-component interventions. Based on these findings, Resources for Enhancing Alzheimer’s Caregiver Health II (REACH II), an intensive and individualised intervention with multiple components, was generated. REACH II causes a clear reduction of the stress and burdens faced by care-giving family members . Nevertheless, despite its advantages and proven effectiveness, it has not been applied to German-speaking areas.
Hence, the planned study aims at the adaptation of the American REACH II intervention to the conditions of the German health-care system in the Deutsche Adaption der Resources for Enhancing Alzheimer’s Caregiver Health (DeREACH), as well as the evaluation of the DeREACH intervention (the official agreement of the developers of REACH II with this intention is on hand).
We assume that the DeREACH intervention as opposed to the standard supply of health-care services will reduce the burden of informal caregivers. Furthermore, positive effects on depression and somatisation as well as health-related quality of life and social support for care-giving family members can be expected.
The study has been designed as a non-blinded, randomised, and controlled trial. The intervention group receives the DeREACH intervention and the control group receives the standard supply of health-care services; both groups receive baseline, final, and follow-up assessments.
The design, conduct, and reporting of the DeREACH study will adhere to the Consolidation Standards of Reporting Trials (CONSORT) guidelines .
Inclusion and exclusion criteria
We only include informal caregivers of people with dementia who live at home with their relatives and are residents of Leipzig. In addition, participants must be able to speak German fluently and a diagnosis of dementia should have been established by a physician for each care recipient.
Recruitment of participants
The recruitment process is supported by the Geriatric and Gerontopsychiatric Network of Leipzig. This network was established to advance the collaboration of various health-care systems and to assure that people with dementia in particular receive constant attention. It involves memory clinics, home-care agencies, nursing homes, voluntary helpers, associations, and day-care facilitates. These participating facilities suggest eligible subjects, inviting them to attend the study. Furthermore, we address potential participants via articles and announcements in newspapers and via posters and flyers that are available in several health-care facilities.
The participants are split into the study groups randomly. To obtain the same number of subjects in the intervention and the control group, we use a randomisation in blocks . Moreover, we use a central randomisation via randomisation lists realised by an online procedure of the Medical Faculty of the Ludwig-Maximilians-University of Munich . The outcome rater is not informed about the randomisation code of a participant before opening a sealed envelope with the code inside after completion of the baseline assessment.
The informal caregivers, their relatives with dementia, and the study staff cannot be blinded in matters related to the study group.
A nurse from University Hospital Leipzig makes contact with our participants and arranges the first appointment. One or two outcome raters visit informal caregivers at home to conduct the baseline assessment. In addition, we undertake a dementia screening for diagnosing the degree of cognitive impairment . This takes place during the first appointment at home with the diseased individual to confirm the diagnosis of dementia.
After completion of the baseline assessment, an envelope containing the subject’s randomisation code is opened to allocate the participant to the intervention group or control group.
Study staff will make another appointment for the first home visit with the informal caregivers allocated to the intervention group. Altogether, the informal caregivers in the intervention group receive nine home visits and three phone sessions. Every home visit is structured in its sequence and appointments will be scheduled visit by visit. Usually, the whole intervention lasts six months and a post-intervention assessment takes place immediately after completion. A follow-up assessment takes place nine months after the baseline assessment.
The intervention is executed by medical staff (for instance, nurses and occupational therapists). Prior to the intervention, these interventionists obtain training and a manual related to the intervention. Furthermore, they are attended and supported by research staff.
For this trial, the original REACH II intervention will be translated into the German language. Regional distinctions have to be adapted to meet conditions in Germany. Especially with regard to the areas of social support and self-care, it was necessary to include regional facilities and other offers of support. All 12 sessions of the DeREACH intervention are described in a study manual. Departing from the original REACH II intervention, we will train medical staff and not volunteers to perform the intervention. Another feature that required modification was the computer telephone integration system that the REACH II intervention provided to all participants, because the requirements are not available in the study area.
Exemplary structure of an intervention session
Prior to a session, the interventionist reviews the risk worksheet
Brief explanation of the focus of the session and how it will be structured
Explanation of the participation in social support groups
Interventionist checks and evaluates with the caregiver the strategies, material, and use of the handbook offered in previous sessions
Interventionist identifies and initiates a problem-solving approach focusing on the caregiver’s individual risk behaviour or problems
Interventionist provides training in different stress management techniques
Closure for each session:
establishing date/time of next session
briefly reviewing problem areas
briefly reviewing strategies used
helping the caregiver implement strategies in daily routine
At the conclusion of the session, the interventionist completes a protocol of the session
Point of measurement
- caregiver sociodemographics
- sociodemographic data questionnaire
Baseline assessment with regard to people with dementia:
- sociodemographic information
- sociodemographic data questionnaire
- degree of cognitive impairment
- SIDAM score
- caregiver burden
- health-related quality of life
- social support
Secondary outcomes with regard to people with dementia:
- health-care service utilisation
- 1 question
- problem behaviour
Sample size calculation
The calculation of sample size was based on an updated meta-analysis determining the effectiveness of interventions for family caregivers of older adults . In that study, a moderate mean effect size of 0.65 (95% CI [0.46-0.84,]) was determined for multi-component interventions on caregiver burden. Assuming this effect size as significant for DeREACH, which is a multi-component intervention, and using a t-test for two independent samples with a 0.05 two-sided significance level, a sample size of 51 patients per group was calculated to have 90% power for detecting a treatment effect of that size (calculated by G*Power ). Allowing for a drop-out rate of 35%, a total of 69 informal caregivers per group is planned.
All analyses will be conducted using Statistical Packages for Social Sciences (SPSS) version 20.0 for Microsoft Windows. The change from baseline to post-intervention assessment (six months) on the ZBI (primary outcome) will be compared between treatment groups using t-tests for independent samples on all randomised informal caregivers (intention-to-treat population). In case of significant between-group differences at baseline, an analysis of the covariance will be used with the post-intervention score as a dependent variable and treatment group and baseline ZBI score will be used as additional covariates. Several SPSS methods with missing value imputation will be used, including expectation maximisation (EM) and multiple imputations. Secondary analyses of the primary outcome variable will be performed on informal caregivers treated per protocol (PP population). Secondary study outcomes will be subjected to an explorative analysis. Post-hoc analyses will be performed on the primary outcome variable in patient subgroups, defined for instance by age, sex, caregiver education, family relationship and cognitive ability of the care recipient at baseline. Secondary and post-hoc analyses will be explorative without multiplicity adjustment.
The study design, study protocol, procedure and informed consent are approved by the ethics committees of the Leipzig University (ref. 217-12-02072012). Participation is voluntary and all participants will sign informed consent.
The study described in this paper is the first study in Germany to investigate the effectiveness of the adapted REACH programme. A significant reduction in burden for informal caregivers over the trial period is expected as a primary outcome. Feeling burdened is a substantial reason for somatic and mental illness among informal caregivers. The results of this study will provide further evidence to support the feasibility of the DeREACH programme for home-care agencies or other service providers in the German health-care system. The findings of the study will yield valuable information regarding how to manage more effectively problems in family care giving for individuals with dementia. In addition, the findings of this study will provide information for others to implement the DeREACH programme in different areas and different cities and communities.
Recruitment into the study started on 1 October 2012.
The trial is funded by the German Federal Ministry of Health (project number: IIA5-2512FSB552). We acknowledge support from the German Research Foundation (DFG) and the Leipzig University within the programme of Open Access Publishing.
- Pinquart M, Sörensen S: Differences between caregivers and noncaregivers in psychological health and physical health: a meta-analysis. Psychol Aging. 2003, 18: 250-267.View ArticlePubMedGoogle Scholar
- Pinquart M, Sörensen S: Helping caregivers of persons with dementia: which interventions work and how large are their effects?. Int Psychogeriatr. 2006, 18: 577-595. 10.1017/S1041610206003462.View ArticlePubMedGoogle Scholar
- Kurz A, Wilz G: Die Belastung pflegender Angehoeriger bei Demenz. Enstehungsbedingungen und Interventionsmoeglichkeiten. Nervenarzt. 2011, 82: 336-342. 10.1007/s00115-010-3108-3.View ArticlePubMedGoogle Scholar
- Donaldson C, Tarrier N, Burns A: Determinants of carer stress in Alzheimer’s disease. Int J Geriatr Psychiatry. 1998, 13: 248-256. 10.1002/(SICI)1099-1166(199804)13:4<248::AID-GPS770>3.0.CO;2-0.View ArticlePubMedGoogle Scholar
- Gitlin LN, Belle SH, Burgio LD, Czaja SJ, Mahoney D, Gallagher-Thompson D, Burns R, Hauck WW, Zhang S, Schulz R, Ory MG: Effect of multicomponent interventions on caregiver burden and depression: the REACH multisite initiative at 6-month follow-up. Psychol Aging. 2003, 18: 361-374.View ArticlePubMedPubMed CentralGoogle Scholar
- Belle SH, Burgio L, Burns R, Coon D, Czaja SJ, Gallagher-Thompson D, Gitlin LN, Klinger J, Koepke KM, Lee CC, Martindale-Adams J, Nichols L, Schulz R, Stahl S, Stevens A, Winter L, Zhang S: Enhancing the quality of life of dementia caregivers from different ethnic or racial groups: a randomized, controlled trial. Ann Intern Med. 2006, 145: 727-738. 10.7326/0003-4819-145-10-200611210-00005.View ArticlePubMedPubMed CentralGoogle Scholar
- Schulz KF, Altman DG, Moher D: CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials. Int J Surg. 2011, 9: 672-677. 10.1016/j.ijsu.2011.09.004.View ArticlePubMedGoogle Scholar
- Efird J: Blocked randomization with randomly selected block sizes. Int J Environ Res Public Health. 2011, 8: 15-20.View ArticlePubMedGoogle Scholar
- Randoulette. https://wwwapp.ibe.med.uni-muenchen.de/randoulette/,
- Zaudig M, Mittelhammer J, Hiller W: SIDAM-Strukturiertes Interview für die Diagnose einer Demenz vom Alzheimer-Typ, Multiinfarktdemenz und Demenzen anderer Ätiologie nach DSM-III-R und ICD-10. 1989, Göttingen: Testzentrale BDPGoogle Scholar
- Epidemiology Data Center of the University of Pittsburgh. http://www.edc.gsph.pitt.edu/Reach2/public/,
- Marim CM, Silva V, Taminato M, Barbosa DA: Effectiveness of educational programs on reducing the burden of caregivers of elderly individuals with dementia: a systematic review. Rev Lat Am Enfermagem. 2013, 21: 267-275. 10.1590/S0104-11692013000700033.View ArticlePubMedGoogle Scholar
- Moniz-Cook E, Vernooij-Dassen M, Woods R, Verhey F, Chattat R, De Vugt M, Mountain G, O’Connell M, Harrison J, Vasse E, Dröes RM, Orrell M, INTERDEM Group: A European consensus on outcome measures for psychosocial intervention research in dementia care. Aging Ment Health. 2008, 12: 14-29. 10.1080/13607860801919850.View ArticlePubMedGoogle Scholar
- Braun M, Scholz U, Hornung R, Martin M: Die subjektive Belastung pflegender Ehepartner von Demenzkranken. Hinweise zur Validität der deutschen Version des Zarit Burden Interviews. Z Gerontol Geriatr. 2010, 43: 111-119. 10.1007/s00391-010-0097-6.View ArticlePubMedGoogle Scholar
- Löwe B, Wahl I, Rose M, Spitzer C, Glaesmer H, Wingenfeld K, Schneider A, Brähler E: A 4-item measure of depression and anxiety: validation and standardization of the Patient Health Questionnaire-4 (PHQ-4) in the general population. J Affect Disord. 2010, 122: 86-95. 10.1016/j.jad.2009.06.019.View ArticlePubMedGoogle Scholar
- Kocalevent R, Hinz A, Brähler E: Standardization of a screening instrument (PHQ-15) for somatization syndromes in the general population. BMC Psychiatry. 2013, 13: 91-10.1186/1471-244X-13-91.View ArticlePubMedPubMed CentralGoogle Scholar
- Morfeld M, Bullinger M, Nantke J, Brähler E: Die Version 2.0 des SF-36 Health Survey – Ergebnisse einer bevölkerungsrepräsentativen Studie. Soz.-Präventivmed. 2005, 50: 292-300. 10.1007/s00038-005-4090-6.View ArticlePubMedGoogle Scholar
- Cordes A, Herrmann-Lingen C, Büchner B, Hessel A: Repräsentative Nominierung des ENRICHD-Social-Support-Instrument (ESSI) – Deutsche Version. Klinische Diagnostik und Evaluation. 2009, 1: 16-32.Google Scholar
- Teri L, Truax P, Logsdon R, Uomoto J, Zarit S, Vitaliano PP: Assessment of behavioral problems in dementia: the revised memory and behavior problems checklist. Psychol Aging. 1992, 7: 622-631.View ArticlePubMedGoogle Scholar
- Sörensen S, Pinquart M, Duberstein P: How effective are interventions with caregivers? An updated meta-analysis. The Gerontologist. 2002, 42: 356-372. 10.1093/geront/42.3.356.View ArticlePubMedGoogle Scholar
- Faul F, Erdfelder E, Lang A-G, Buchner A: G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav Res Methods. 2007, 39: 175-191. 10.3758/BF03193146.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2318/14/21/prepub
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