Randomized clinical trial of the Timing it Right Stroke Family Support Program: research protocol

Jill I Cameron, Gary Naglie, Monique A M Gignac, Mark Bayley, Grace Warner, Theresa Green, Anna Czerwonka, Maria Huijbregts, Frank L Silver, Steve J Phillips, Angela M Cheung, Jill I Cameron, Gary Naglie, Monique A M Gignac, Mark Bayley, Grace Warner, Theresa Green, Anna Czerwonka, Maria Huijbregts, Frank L Silver, Steve J Phillips, Angela M Cheung

Abstract

Background: Family caregivers provide invaluable support to stroke survivors during their recovery, rehabilitation, and community re-integration. Unfortunately, it is not standard clinical practice to prepare and support caregivers in this role and, as a result, many experience stress and poor health that can compromise stroke survivor recovery and threaten the sustainability of keeping the stroke survivor at home. We developed the Timing it Right Stroke Family Support Program (TIRSFSP) to guide the timing of delivering specific types of education and support to meet caregivers' evolving needs. The objective of this multi-site randomized controlled trial is to determine if delivering the TIRSFSP across the stroke care continuum improves caregivers' sense of being supported and emotional well-being.

Methods/design: Our multi-site single-blinded randomized controlled trial will recruit 300 family caregivers of stroke survivors from urban and rural acute care hospitals. After completing a baseline assessment, participants will be randomly allocated to one of three groups: 1) TIRSFSP guided by a stroke support person (health care professional with stroke care experience), delivered in-person during acute care and by telephone for approximately the first six to 12 months post-stroke, 2) caregiver self-directed TIRSFSP with an initial introduction to the program by a stroke support person, or 3) standard care receiving the educational resource "Let's Talk about Stroke" prepared by the Heart and Stroke Foundation. Participants will complete three follow-up quantitative assessments 3, 6, and 12-months post-stroke. These include assessments of depression, social support, psychological well-being, stroke knowledge, mastery (sense of control over life), caregiving assistance provided, caregiving impact on everyday life, and indicators of stroke severity and disability. Qualitative methods will also be used to obtain information about caregivers' experiences with the education and support received and the impact on caregivers' perception of being supported and emotional well-being.

Discussion: This research will determine if the TIRSFSP benefits family caregivers by improving their perception of being supported and emotional well-being. If proven effective, it could be recommended as a model of stroke family education and support that meets the Canadian Stroke Best Practice Guideline recommendation for providing timely education and support to families through transitions.

Trial registration: ClinicalTrials.gov: NCT00958607.

Figures

Figure 1
Figure 1
Timing it right framework (Cameron and Gignac, 2008).
Figure 2
Figure 2
Anticipated CONSORT diagram including follow-up protocol and qualitative data collection.

References

    1. Heart and Stroke Foundation. 2013 Stroke Report. .
    1. Mayo NE, Wood-Dauphinee S, Cote R, Durcan L, Carlton J. Activity, participation, and quality of life 6 months poststroke. Arch Phys Med Rehabil. 2002;14:1035–1042. doi: 10.1053/apmr.2002.33984.
    1. Smith JE, Smith DL. No map, no guide. Family caregivers’ perspectives on their journeys through the system. Care Manag J. 2000;14:27–33.
    1. Schulz R, O'Brien AT, Bookwala J, Fleissner K. Psychiatric and physical morbidity effects of dementia caregiving: prevalence, correlates, and causes. Gerontologist. 1995;14:771–791. doi: 10.1093/geront/35.6.771.
    1. Pinquart M, Sorensen S. Differences between caregivers and noncaregivers in psychological health and physical health: a meta-analysis. Psychol Aging. 2003;14:250–267.
    1. Han B, Haley WE. Family caregiving for patients with stroke. Review and analysis. Stroke. 1999;14:1478–1485. doi: 10.1161/01.STR.30.7.1478.
    1. Evans RL, Bishop DS, Haselkorn JK. Factors predicting satisfactory home care after stroke. Arch Phys Med Rehabil. 1991;14:144–147.
    1. Kao HF, McHugh ML. The role of caregiver gender and caregiver burden in nursing home placements for elderly Taiwanese survivors of stroke. Res Nurs Health. 2004;14:121–134. doi: 10.1002/nur.20007.
    1. Arai Y, Sugiura M, Washio M, Miura H, Kudo K. Caregiver depression predicts early discontinuation of care for disabled elderly at home. Psychiatry Clin Neurosci. 2001;14:379–382. doi: 10.1046/j.1440-1819.2001.00878.x.
    1. Clarke A, Rosen R. Length of stay. How short should hospital care be? Eur J Public Health. 2001;14:166–170. doi: 10.1093/eurpub/11.2.166.
    1. Wilkins K, Park E. Home care in Canada. Health Rep. 1998;14:29–37.
    1. Bergman H, Beland F, Lebel P, Contandriopoulos AP, Tousignant P, Brunelle Y. et al.Care for Canada’s frail elderly population: fragmentation or integration? CMAJ. 1997;14:1116–1121.
    1. Visser-Meily A, van Heugten C, Post M, Schepers V, Lindeman E. Intervention studies for caregivers of stroke survivors: a critical review. Patient Educ Couns. 2005;14:257–267. doi: 10.1016/j.pec.2004.02.013.
    1. Greenwood N, Mackenzie A, Cloud GC, Wilson N. Informal primary carers of stroke survivors living at home - challenges, satisfactions and coping: a systematic review of qualitative studies. Disabil Rehabil. 2008;14:1–15.
    1. Cameron JI, Naglie G, Silver FL, Gignac MA. Stroke family caregivers’ support needs change across the care continuum: a qualitative study using the timing it right framework. Disabil Rehabil. 2013;14:315–324. doi: 10.3109/09638288.2012.691937.
    1. Cameron JI, Gignac MA. “Timing It right”: a conceptual framework for addressing the support needs of family caregivers to stroke survivors from the hospital to the home. Patient Educ Couns. 2008;14:305–314. doi: 10.1016/j.pec.2007.10.020.
    1. Evans RL, Matlock AL, Bishop DS, Stranahan S, Pederson C. Family intervention after stroke: does counseling or education help? Stroke. 1988;14:1243–1249. doi: 10.1161/01.STR.19.10.1243.
    1. Lincoln NB, Francis VM, Lilley SA, Sharma JC, Summerfield M. Evaluation of a stroke family support organiser: a randomized controlled trial. Stroke. 2003;14:116–121. doi: 10.1161/01.STR.0000047850.33686.32.
    1. Grant JS, Elliott TR, Weaver M, Bartolucci AA, Giger JN. Telephone intervention with family caregivers of stroke survivors after rehabilitation. Stroke. 2002;14:2060–2065. doi: 10.1161/01.STR.0000020711.38824.E3.
    1. van den Heuvel ET, Witte LP, Stewart RE, Schure LM, Sanderman R, Meyboom-de Jong B. Long-term effects of a group support program and an individual support program for informal caregivers of stroke patients: which caregivers benefit the most? Patient Educ Couns. 2002;14:291–299. doi: 10.1016/S0738-3991(01)00230-0.
    1. Braithwaite V, McGown A. Caregivers’ emotional well-being and their capacity to learn about stroke. J Adv Nurs. 1993;14:195–202. doi: 10.1046/j.1365-2648.1993.18020195.x.
    1. Rodgers H, Atkinson C, Bond S, Suddes M, Dobson R, Curless R. Randomized controlled trial of a comprehensive stroke education program for patients and caregivers. Stroke. 1999;14:2585–2591. doi: 10.1161/01.STR.30.12.2585.
    1. Dennis M, O’Rourke S, Slattery J, Staniforth T, Warlow C. Evaluation of a stroke family care worker: results of a randomised controlled trial. Br Med J. 1997;14:1071–1076. doi: 10.1136/bmj.314.7087.1071.
    1. Cohen S. In: The meaning and measurement of social support. Veiel HOF, Baumann A, editor. New York: Hemisphere Publishing Corporation; 1992. Stress, social support, and disorder; pp. 109–124.
    1. Aneshensel CS, Stone JD. Stress and depression: a test of the buffering model of social support. Arch Gen Psychiatry. 1982;14:1392–1396. doi: 10.1001/archpsyc.1982.04290120028005.
    1. Drentea P, Clay OJ, Roth DL, Mittelman MS. Predictors of improvement in social support: five-year effects of a structured intervention for caregivers of spouses with Alzheimer’s disease. Soc Sci Med. 2006;14:957–967. doi: 10.1016/j.socscimed.2006.02.020.
    1. Bass DM, Noelker LS, Rechlin LR. The moderating influence of service use on negative caregiving consequences. J Gerontol. 1996;14:S121–S131. Series B, Psychological Sciences & Social Sciences.
    1. Cutrona CE, Russell DW. In: Social support: an interactional view. Saranson BR, Saranson IG, Pierce GR, editor. New York: Wiley; 1990. Type of social support and specific stress: towards a theory of optimal matching; pp. 319–366.
    1. Sorensen S, Pinquart M, Duberstein P. How effective are interventions with caregivers? An updated meta-analysis. Gerontologist. 2002;14:356–372. doi: 10.1093/geront/42.3.356.
    1. Eames S, Hoffmann T, Worrall L, Read S, Wong A. Randomised controlled trial of an education and support package for stroke patients and their carers. BMJ Open. 2013;14:1–9.
    1. King RB, Hartke RJ, Houle T, Lee J, Herring G, Exander-Peterson BS. et al.A problem-solving early intervention for stroke caregivers: one year follow-up. Rehabil Nurs. 2012;14:231–243. doi: 10.1002/rnj.039.
    1. Teng J, Mayo NE, Latimer E, Hanley J, Wood-Dauphinee S, Cote R. et al.Costs and caregiver consequences of early supported discharge for stroke patients. Stroke. 2003;14:528–536. doi: 10.1161/01.STR.0000049767.14156.2C.
    1. Sulch D, Melbourn A, Perez I, Kalra L. Integrated care pathways and quality of life on a stroke rehabilitation unit. Stroke. 2002;14:1600–1604. doi: 10.1161/01.STR.0000017144.04043.87.
    1. Grant JS. Social problem-solving partnerships with family caregivers. Rehabil Nurs. 1999;14:254–260. doi: 10.1002/j.2048-7940.1999.tb02192.x.
    1. Boter H. for the HESTIA Study Group. Multicenter randomized controlled trial of an outreach nursing support program for recently discharged stroke patients. Stroke. 2004;14:2867–2872. doi: 10.1161/01.STR.0000147717.57531.e5.
    1. Kodner DL, Spreeuwenberg C. Integrated care: meaning, logic, applications, and implications: a discussion paper. Int J Int Care. 2002;14:1–8.
    1. Reuben DB, Eng C, Pedulla J, Eleazer GP, McCann R, Fox N. Models of geriatric practice: program of all-inclusive care for the elderly (PACE): an innovative model of integrated geriatric care and financing. J Am Geriatr Soc. 1997;14:1–20.
    1. Hebert R, Durand PJ, Dubuc N, Tourigny A. PRISMA: a new model of integrated service delivery for the frail older people in Canada. Int J Int Care. 2003;14:1–10.
    1. Coleman EA, Parry C, Chalmers S, Min SJ. The care transitions intervention: results of a randomized controlled trial. Arch Intern Med. 2006;14:1822–1828. doi: 10.1001/archinte.166.17.1822.
    1. Parry C, Coleman EA, Smith JD, Frank J, Kramer AM. The care transitions intervention: a patient-centered approach to ensuring effective transfers between sites of geriatric care. Home Health Care Serv Q. 2003;14:1–17.
    1. Creswell J, Plano Clark V. Designing and conducting mixed methods research: second edition. 2. California: Sage Publications, Inc; 2011.
    1. Jones F. Strategies to enhance chronic disease self-management: how can we apply this to stroke? Disabil Rehabil. 2006;14:841–847. doi: 10.1080/09638280500534952.
    1. Lorig KR, Holman H. Self-management education: history, definition, outcomes, and mechanisms. Ann Behav Med. 2003;14:1–7. doi: 10.1207/S15324796ABM2601_01.
    1. Cameron JI, Naglie G, Green TL, Gignac MA, Bayley M, Huijbregts M, Development and pilot testing of the timing it right stroke family support program. 2014. Manuscript in preparation.
    1. Cameron JI, Franche RL, Cheung AM, Stewart DE. Lifestyle interference and emotional distress in family caregivers of advanced cancer patients. Cancer. 2002;14:521–527. doi: 10.1002/cncr.10212.
    1. Cameron JI, Herridge MS, Tansey CM, McAndrews MP, Cheung AM. Well-being in informal caregivers of survivors of acute respiratory distress syndrome. Crit Care Med. 2006;14:81–86. doi: 10.1097/01.CCM.0000190428.71765.31.
    1. Cameron JI, Cheung AM, Streiner DL, Coyte PC, Stewart DE. Stroke survivor depressive symptoms are associated with family caregiver depression during the first 2 years poststroke. Stroke. 2011;14:302–306. doi: 10.1161/STROKEAHA.110.597963.
    1. EmPOWER. EmPower health research inc. 2009. Ref Type: Computer Program.
    1. Sherbourne CD, Stewart AL. The MOS social support survey. Soc Sci Med. 1991;14:705–714. doi: 10.1016/0277-9536(91)90150-B.
    1. Watson D, Clark LA, Tellegen A. Development and validation of brief measures of positive and negative affect: the PANAS scales. J Personal Soc Psychol. 1988;14:1063–1070.
    1. Radloff LS. The CES-D scale: a self-report depression scale for research in the general population. Appl Psychol Measure. 1977;14:385–401. doi: 10.1177/014662167700100306.
    1. Cameron JI, Cheung AM, Streiner DL, Coyte PC, Stewart DE. Stroke survivors’ behavioral and psychologic symptoms are associated with informal caregivers’ experiences of depression. Arch Phys Med Rehabil. 2006;14:177–183. doi: 10.1016/j.apmr.2005.10.012.
    1. Sullivan K, Dunton NJ. Development and validation of the stroke knowledge test. Top Stroke Rehabil. 2004;14:19–28. doi: 10.1310/RED5-V47T-8MJN-JY9H.
    1. Pearlin LI, Schooler C. The structure of coping. J Health Soc Behav. 1978;14:2–21. doi: 10.2307/2136319.
    1. Pearlin LI, Mullan JT, Semple SJ, Skaff MM. Caregiving and the stress process: an overview of concepts and their measures. Gerontologist. 1990;14:583–594. doi: 10.1093/geront/30.5.583.
    1. Browne GB, Arpin K, Corey P, Fitch M, Gafni A. Individual correlates of health service utilization and the cost of poor adjustment to chronic illness. Med Care. 1990;14:43–58. doi: 10.1097/00005650-199001000-00006.
    1. Cote R, Battista RN, Wolfson C, Boucher J, Adam J, Hachinski V. The Canadian neurological scale: validation and reliability assessment. Neurology. 1989;14:638–643. doi: 10.1212/WNL.39.5.638.
    1. Wade DT, Hewer RL. Functional abilities after stroke: measurement, natural history and prognosis. J Neurol Neurosurg Psychiatry. 1987;14:177–182. doi: 10.1136/jnnp.50.2.177.
    1. Sturges JE, Hanrahan KJ. Comparing telephone and face-to-face qualitative interviewing: a research note. Qual Res. 2004;14:107–118. doi: 10.1177/1468794104041110.
    1. Rabiee F. Focus-group interview and data analysis. Proc Nutr Soc. 2004;14:655–660. doi: 10.1079/PNS2004399.
    1. Ritchie J, Spencer L. In: Analyzing qualitative data. Bryman A, Burgess RG, editor. New York, NY: Routledge; 1994. Qualitative data analysis for applied policy research; pp. 173–194.
    1. Tabachnick BG, Fidell LS. Using multivariate statistics. 3. New York, NY: HarperCollins College Publishers; 2001.
    1. Creswell JW. Qualitative inquiry and research design: choosing among five traditions. London: Sage Publications; 1998.
    1. McReynolds CJ, Koch LC, Rumrill PD Jr. Speaking of research. Qualitative research strategies in rehabilitation. Work. 2001;14:57–65.
    1. Singer JD, Willett JB. Applied longitudinal data analysis: modeling change and event occurrence. New York: Oxford University Press, Inc; 2003.
    1. NVivo qualitative data analysis software. [10.0] QSR international Pty Ltd. 2012. Ref Type: Computer Program.
    1. Hsieh HF, Shannon SE. Three approaches to qualitative content analysis. Qual Health Res. 2005;14:1277–1288. doi: 10.1177/1049732305276687.
    1. Neuendorf KA. The content analysis guidebook. Thousand Oaks (CA): Sage; 2002.
    1. Lindsay MP, Gubitz G, Bayley M, Hill MD, Davies-Schinkel C, Singh S, Canadian best practice recommendations for stroke care (update 2010). Canadian stroke strategy best practices and standards writin group. Ottawa, Canada: Canadian Stroke Network; 2010. Ref Type: Report.

Source: PubMed

3
Suscribir