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2.
Omega (Westport) ; 67(1-2): 53-61, 2013.
Article in English | MEDLINE | ID: mdl-23977779

ABSTRACT

Family caregivers often suffer higher levels of physical and emotional distress when caring for a chronically or terminally ill family member. Providing this kind of care to a loved one at the end of life contributes to increased stress, health problems, and a decreased quality of life. The Hospice Caregiver Support Project provided support services to caregivers identified by the hospice social worker as needing this support and/or assistance. Results from the project show that offering additional services relieved caregiver stress by allowing the caregiver time away from their caregiving role and reducing feelings of guilt and worry, and increased hospice social worker satisfaction with their ability to respond to the needs of hospice patients and caregivers.


Subject(s)
Caregivers/psychology , Interpersonal Relations , Palliative Care/organization & administration , Social Support , Stress, Psychological/prevention & control , Adaptation, Psychological , Adult , Aged , Counseling/methods , Female , Follow-Up Studies , Health Status , Humans , Male , Middle Aged , Palliative Care/psychology , Program Evaluation , Quality of Life/psychology
3.
J Palliat Med ; 14(5): 593-7, 2011 May.
Article in English | MEDLINE | ID: mdl-21438707

ABSTRACT

INTRODUCTION: The vast majority (80%) of care provided to hospice patients is given by informal and unpaid caregivers, who are often family members. They may be responsible for everything from management of the household and finances to medical and personal care. Providing this kind of care to a loved one at the end of life can contribute to increased stress, health problems, and decreased quality of life. METHODS: Hospice social workers referred caregivers identified as needing additional support into a special project that funded services not covered by hospice and that the family could not afford to purchase. There were no restrictions on the types of services that could be requested. The Pearlin role overload measure (ROM) was administered and the family selected a service provider from an approved list of agencies. Upon completion of the service period, the ROM was re-administered. Use of the hospice respite benefit by any hospice patient during this study was compared with use before the project began. RESULTS: Self-reported caregiver stress, as measured by the Pearlin ROM pre- and post-services, decreased by 52% (t(122) = 10.254; p < 0.0001). Use of the hospice respite benefit requested by any hospice patient caregiver decreased during the project period (χ(2), p < 0.02), and when respite was requested fewer days were used as compared with the same time period prior to the project (χ(2), p < 0.0043). CONCLUSION: The project results show that offering such services relieved caregiver stress, reduced use of respite, and reduced the number of respite days used.


Subject(s)
Caregivers/psychology , Hospices , Social Support , Stress, Psychological/prevention & control , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Surveys and Questionnaires
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