Perceived physical health in family caregivers of Alzheimer patientsMediator variables

  1. Díaz Martinez, Amelia
  2. Ponsoda Tornal, José Manuel
Revista:
European Journal of Health Research: (EJHR)

ISSN: 2444-9067,  2445-0308

Any de publicació: 2017

Volum: 3

Número: 1

Pàgines: 5-15

Tipus: Article

DOI: 10.1989/EJHR.V3I1.51 DIALNET GOOGLE SCHOLAR lock_openDialnet editor

Altres publicacions en: European Journal of Health Research: (EJHR)

Resum

The aim of this work is to know the mediating role of such variables as social support and cope as other associated with Positive Psychology in family caregivers of Alzheimer patients. Method: Participants: 140 caregivers of Alzheimer patients. Instruments: Sociodemographic data; CBI Caregiver Burden Scale; COPE Coping Styles Scale; DUKE.UNC Social Support Scale; QOLLTI-F, Quality of Life in Life Threatening Illness Scale–Family Carers Version; SHS, Subjective Happiness Scale; SWLS, Satisfaction with Life Scale. Results: The most relevant results refer to the partial mediating role of happiness, quality of life and life satisfaction variables between subjective burden and perceived physical health. Conclusions and discussion: Positive Psychology variables such as happiness, quality of life and life satisfaction have shown a mediating role between the perception that Alzheimer's caregivers have of care burden and physical health. We believe that this finding is an important step in the future development and implementation of intervention programs for caregivers that promote variables with positive connotation, because they would change the perception of their own burden and physical health, making them happier and with greater satisfaction and quality of life.

Referències bibliogràfiques

  • Aneshensel, C., Pearlin, L., Mullan, J., Zarit, S.H., & Whitlatch, C.J. (1995). Profiles in caregiving:The unexpected career. New York, NY: Academic Press.
  • Artaso, B., Goñi, A., & Biurrun, A. (2003). Cuidados informales en la demencia: predicción desobrecarga en cuidadoras familiares. [Informal caring in dementia patients: Burden prediction in family caregivers]. Revista Española de Geriatría y Gerontología, 38, 212-218.
  • Badía, X., Lara, N., & Roset, M. (2004). Calidad de vida, tiempo de dedicación y carga percibidapor el cuidador principal informal del enfermo de Alzheimer. [Quality of life, time caring and perceived burden in the primary informal caregiver of Alzheimer patients]. Atención Primaria, 34, 170-177.
  • Belle, S.H., Burgio, L., Burns, R., Coon, D., Czaja, S.J., Gallagher-Thompson, D., … Zhang, S. (2006). Enhancing the quality of life of dementia caregivers from different ethnic or racial groups: a randomized, controlled trial. Annals of Internal Medicine, 145, 727-38.
  • Bower, J.E., Kemeny, M.E., Taylor, S.E., & Fahey, J.L. (1998). Cognitive processing, discovery of meaning, CD4 decline, and AIDS related mortality among bereaved HIV-seropositive men. Journal of Consulting and Clinical Psychology, 66, 979-986.
  • Biurrun, A., Artaso, B., & Goñi, A. (2003). Apoyo social en cuidadores familiares de enfermos con demencia [Social support in family caragivers of dementia patients]. Geriatrika, 19, 181-187.
  • Broadhead, W.E., Gehlbach, S.H., Degruy, F.V., & Kaplan, B.H. (1988). The Duke-UNC Functional Social Support Questionnaire: Measurement for social support in family medicine patients. Medicine Care, 26, 709-723.
  • Carver, C.S. (1997). You want to measure coping but your protocol´s too long: Consider the Brief COPE. International Journal of Behavioral Medicine, 4, 92-100.
  • Cohen, R., Leis, A.M., Kuhl, D., Charbonneau, C., Ritvo, P., & Ashbury, F.D. (2006). QOLLTI-F: Measuring family carer quality of life. Palliative Medicine, 20, 755-767.
  • Cohen, S., Doyle, W.J., Turner, R.B., Alper, C.M., & Skoner, D.P. (2003). Emotional Style and Susceptibility to the Common Cold. Psychosomatic Style, 65, 652-657.
  • Colmenero, C.J., Peláez, E.M., & Muela, J.A. (2002). Comparación entre distintas clasificaciones de las estrategias de afrontamiento en cuidadores de enfermos de Alzheimer [Comparison between different coping styles classifications in caregivers of Alzheimer patients]. Psicothema, 14, 558-563.
  • Crespo, M., & López, J. (2007). El estrés en cuidadores de mayores dependientes [Stress in caregivers of dependent eldery people]. Madrid: Pirámide.
  • Danner, D.D., Snowdon, D.A., & Friesen, W.V. (2001). Positive emotions in early life and longevity: Findings from the nun study. Journal of Personality and Social Psychology, 80, 804-813.
  • Diener, E., Emmons, R., Larsen, R.J., & Griffin, S. (1985). The Satisfaction with Life Scale. Journal of Personality Assessment, 49, 71-75.
  • Gable, S.L., & Haidt, J. (2005). What (and why) is Positive Psychology? Review of General Psychology, 9, 103-110.
  • García, M.M., Mateo, I., & Maroto, G. (2004). El impacto de cuidar en la salud y la calidad de vida de las mujeres [The impact of caring in the health and quality of life of women]. Gaceta Sanitaria, 18, 83-92.
  • Gaugler, J.E., Zarit, S.H., & Pearlin, L.I. (1999). Caregiving and institutionalization: Perceptions of family conflict and socioemotional support. The International Journal of Aging and Human Development, 49, 1-25.
  • Gillham, J.E., & Seligman M.E.P. (1999) Footsteps on the road to a positive psychology. Behavior Research and Therapy, 37, 163-173.
  • Harker, L., & Keltner, D. (2001). Expressions of positive emotion in women’s college yearbook pictures and their relationship to personality and life outcomes across adulthood. Journal of Personality and Social Psychology, 80, 112-124.
  • Korn, L., Logsdon, R., Polissar, N., Gomez-Beloz, A., Waters, T., & Rÿser, R. (2009). A Randomized Trial of a CAM Therapy for Stress Reduction in American Indian and Alaskan Native Family Caregivers. The Gerontologist 49, 368-377.
  • Lanzón, T., & Díaz, A. (2014). Predictive role of caregiver type, dependency level and time caring on the impact of caring for a dependent relative as a stressor. European Journal of Investigation in Health, Psychology and Education, 4, 193-202.
  • Lyubomirsky, S., & Lepper, H.S. (1999). A measure of subjective happiness: Preliminary reliability and construct validation. Social Indicators Research, 46, 137-155.
  • Mears R., & Sánchez, S. (2005). Necesidades del cuidador del enfermo de Alzheimer Terminal [The caregiver´s needs of terminal Alzheimer patient]. Enfermería Global, 7, 1-26.
  • Muela, J.A., Torres, C.J., & Peláez, E.M. (2002). Nuevo instrumento de evaluación de situaciones estresantes en cuidadores de enfermos de Alzheimer. [New instrument in the assessment of stress situations for caregivers of Alzheimer patients]. Alzheimer, 18, 34-36.
  • Novak, M., & Guest, C. (1989). Caregiver response to Alzheimer’s disease. International Journal of Aging and Human Development, 28, 67-79.
  • Novak, M., & Guest, C. (1992). A comparison of the impact of institutionalization on spouse and non-spouse caregivers. The Journal of Applied Gerontology, 11, 379-394.
  • Pearlin, L.I. (1992). The careers of caregivers. The Gerontologist, 32, 647.
  • Pearlin, L.I., & Skaff, M.M. (1995). Stressors in adaptation in late life. In M. Gatz (Ed.), Emerging issues in mental health and aging (pp. 97-123). Washington, DC: APA.
  • Peña-Casanova, J. (1999). Enfermedad de Alzheimer. Del diagnóstico a la terapia: Conceptos y hechos [Alzheimer's disease. From diagnosis to therapy. Concept and facts]. Barcelona: Fundación La Caixa.
  • Reed, G.M., Kemeny, M.E., Taylor, S.E., & Visscher, B.R. (1999). Negative HIV-specific expectancies and AIDS-related bereavement as predictors of symptom onset in asymptomatic HIVpositive gay men. Health Psychology, 18, 354-363.
  • Rodríguez del Álamo, A. (2002). Factores de riesgo de sobrecarga en los familiares cuidadores de enfermos de Alzheimer [Burden risk´s factors in family caregivers of Alzheimer patients]. Alzheimer, 28, 34-36.
  • Rogero-García, J. (2010). Los tiempos del cuidado. El impacto de la dependencia de los mayores en la vida cotidiana de sus cuidadores [Caring times.The impact of elderly dependency in the daily life of caregivers]. Madrid: IMSERSO.
  • Seligman, M.E.P. (1999). The president’s address. American Psychologist, 54, 559-562.
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