Literature DB >> 16910811

Interest in research participation among hospice patients, caregivers, and ambulatory senior citizens: practical barriers or ethical constraints?

Charlotte J Williams1, John L Shuster, Olivio J Clay, Kathryn L Burgio.   

Abstract

OBJECTIVES: The purpose of this survey study was to explore hypothetical interest in research participation among hospice patients and caregivers compared to ambulatory senior citizens.
DESIGN: Cross-sectional survey.
SETTING: Twenty-one community-based hospice offices, a university medical center geriatric ambulatory care clinic, and 3 community-based senior citizen centers. PARTICIPANTS: Participants were hospice patients, caregivers, and ambulatory senior citizens not enrolled in hospice. MEASUREMENTS: Using a self-administered questionnaire, participants rated their interest in participating in survey/interview and therapeutic studies, identified potential benefits and barriers to research participation, and reported their preferences for who they would want to approach them about research participation.
RESULTS: Forty-six percent of hospice patients and 60% of caregivers reported an interest in interview or survey research participation; 45% and 57%, respectively, expressed interest in therapeutic research. Compared to hospice patients, caregivers reported higher rates of personal interest in both survey research (p =< 0.001) and therapeutic research (p=<0.001) and were more likely to report that the hospice patients they cared for would be interested (p = 0.005 and p = 0.027). Younger hospice patients were more favorably disposed toward both survey and therapeutic research participation than hospice patients over the age of 75 (p = 0.063 and 0.011). The proportion of older hospice patients showing interest in research did not differ significantly from ambulatory senior citizens for either type of research (p = 0.56, 0.98).
CONCLUSION: This study suggests that many hospice patients are interested in research participation and are able to articulate benefits and barriers, which supports the inclusion of this population in research.

Entities:  

Mesh:

Year:  2006        PMID: 16910811     DOI: 10.1089/jpm.2006.9.968

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  9 in total

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Review 6.  Dying persons' perspectives on, or experiences of, participating in research: An integrative review.

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Authors:  Elizabeth A Hahn; Phillip A Ianni; Robin A Hanks; Jennifer A Miner; Jenna Freedman; Noelle E Carlozzi
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9.  Patient, caregiver, health professional and researcher views and experiences of participating in research at the end of life: a critical interpretive synthesis of the literature.

Authors:  Marjolein H Gysels; Catherine Evans; Irene J Higginson
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  9 in total

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