Abstract
Peer-delivered health models may hold important benefits for family members, yet their prevalence, components, and outcomes are unknown. We conducted a review of peer-delivered services for families of children and adults with serious health problems. Studies of interventions published between 2000 and 2016 were included if the intervention contained a component for family members. Of 88 studies that were assessed for their eligibility, five met criteria. Familial components included information about the health condition and management, strategies to enhance communication and stress, and the provision of emotional support. Outcomes were largely favorable, including reductions in distress and symptoms of trauma, enhanced quality of life, and positive perceptions of the peer therapeutic alliance. Peer-delivered services for family members may hold important benefits to caregivers; however, the research base remains thin. A research agenda to develop and examine these models is discussed.
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Acri, M., Hooley, C.D., Richardson, N., & Moaba, L.B. (2016). Peer models in mental health for caregivers and families. Community Mental Health Journal, 1–9.
Adelman, R. D., Tmanova, L. L., Delgado, D., Dion, S., & Lachs, M. S. (2014). Caregiver burden: A clinical review. The Journal of the American Medical Association, 311(10), 1052–1060.
Allicock, M., Carr, C., Johnson, L. S., Smith, R., Lawrence, M., Kaye, L., et al. (2014). Implementing a one-on-one peer support program for cancer survivors using a motivational interviewing approach: Results and lessons learned. Journal of Cancer Education, 29(1), 91–98.
Brodaty, H., & Donkin, M. (2009). Family caregivers of people with dementia. Dialogues in Clinical Neuroscience, 11(2), 217.
Brown, R. T., Wiener, L., Kupst, M. J., Brennan, T., Behrman, R., Compas, B. E., et al. (2008). Single parents of children with chronic illness: An understudied phenomenon. Journal of Pediatric Psychology, 33(4), 408–421.
Chambers, S. K., Schover, L., Halford, K., Ferguson, M., Gardiner, R. A., Occhipinti, S., et al. (2013). ProsCan for couples: A feasibility study for evaluating peer support within a controlled research design. Psycho‐Oncology, 22(2), 475–479.
Davidson, L., Bellamy, C., Guy, K., & Miller, R. (2012). Peer support among persons with severe mental illnesses: A review of evidence and experience. World psychiatry: official journal of the World Psychiatric Association (WPA), 11(2), 123–128.
Davidson, L., Chinman, M., Sells, D., & Rowe, M. (2006). Peer support among adults with serious mental illness: A report from the field. Schizophrenia Bulletin, 32(3), 443–450.
Desai, P. P., Rivera, A. T., & Backes, E. M. (2016). Latino caregiver coping with children’s chronic health conditions: An integrative literature review. Journal of Pediatric Health Care, 30(2), 108–120.
Dixon, L., McFarlane, W. R., Lefley, H., Lucksted, A., Cohen, M., Falloon, I., et al. (2001). Evidence-based practices for services to families of people with psychiatric disabilities. Psychiatric Services, 52(7), 903–910.
Family Caregiver Alliance (2016). A population at risk. https://www.caregiver.org/caregiver-health.
Foster, M., Whitehead, L., & Maybee, P. (2010). Parents’ and health professionals’ perceptions of family centered care for children in hospital, in developed and developing countries: A review of the literature. International Journal of Nursing Studies, 47(9), 1184–1193.
Hoagwood, K., Cavaleri, M. A., Olin, S., Burns, B., Slaton, E., Gruttadaro, D., et al. (2010). Family support in children’s mental health: A review and synthesis. Clinical Child and Family Psychology Review, 13, 1–45.
Hoagwood, K. E., Jensen, P., Acri, M., Olin, S. S., Lewandowski, E., & Herman, R. (2012). Outcome domains in child mental health research since 1996: Have they changed and why does it matter? Journal of the American Academy of Child & Adolescent Psychiatry, 51(12), 1241–1260.
Laks, J., Goren, A., Dueñas, H., Novick, D., & Kahle‐Wrobleski, K. (2016). Caregiving for patients with alzheimer’s disease or dementia and its association with psychiatric and clinical comorbidities and other health outcomes in Brazil. International Journal of Geriatric Psychiatry, 31(2), 176–185.
Murphy, N. A., Christian, B., Caplin, D. A., & Young, P. C. (2007). The health of caregivers for children with disabilities: Caregiver perspectives. Child: Care, Health and Development, 33(2), 180–187.
Neri, L., Lucidi, V., Catastini, P., & Colombo, C. (2015). Caregiver burden and vocational participation among parents’ of adolescents with CF. Pediatric Pulmonology, 51(3), 243–252.
O’Brien, I., Duffy, A., & Nicholl, H. (2009). Impact of childhood chronic illnesses on siblings: A literature review. British Journal of Nursing, 18(22), 1358–1365
Phillips, S. S., Ragas, D. M., Hajjar, N., Tom, L. S., Dong, X., & Simon, M. A. (2016). Leveraging the experiences of informal caregivers to create future healthcare workforce options. Journal of the American Geriatrics Society, 64(1), 174–180.
Preyde, M., & Ardal, F. (2003). Effectiveness of a parent “buddy” program for mothers of very preterm infants in a neonatal intensive care unit. Canadian Medical Association Journal, 168(8), 969–973.
Reinhard, S. C., Given, B., Petlick, N. H., & Bemis, A. (2008). Supporting family caregivers in providing care. In R. G. Hughes (Ed.), Patient safety and quality: An evidence-based handbook for nurses (Chapter 14). Rockville, MD: Agency for Healthcare Research and Quality.
Schulz, R., & Martire, L. M. (2004). Family caregiving of persons with dementia: Prevalence, health effects, and support strategies. The American Journal of Geriatric Psychiatry, 12(3), 240–249.
St. Jude Children’s Research Hospital (2016). What is patient family centered care? https://www.stjude.org/treatment/patient-resources/family-centered-care.html.
Sullivan-Bolyai, S., Bova, C., Leung, K., Trudeau, A., Lee, M., & Gruppuso, P. (2010). Social support to empower parents (STEP) An intervention for parents of young children newly diagnosed with type 1 diabetes. The Diabetes Educator, 36(1), 88–97.
Tam, V. V., Larsson, M., Pharris, A., Diedrichs, B., Nguyen, H. P., & Nguyen, C. T. K., et al. (2012). Peer support and improved quality of life among persons living with HIV on antiretroviral treatment: A randomised controlled trial from north-eastern Vietnam. Health and Quality of Life Outcomes, 10(1), 1.
Yale New Haven Hospital (2016). What is patient and family centered care? https://www.ynhh.org/services/quality-safety/patient-and-family-centered-care.aspx.
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Acri, M., Zhang, S., Adler, J.G. et al. Peer-Delivered Models for Caregivers of Children and Adults with Health Conditions: A Review. J Child Fam Stud 26, 337–344 (2017). https://doi.org/10.1007/s10826-016-0616-1
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DOI: https://doi.org/10.1007/s10826-016-0616-1