Literature DB >> 15662180

Who enrolls in observational end of life research? Report from the cultural variations in approaches to end of life study.

Etienne Phipps1, Diana Harris, Leonard E Braitman, William Tester, Nora Madison-Thompson, Gala True.   

Abstract

BACKGROUND: Response bias in end of life research is important though not well understood.
OBJECTIVES: To compare consenting advanced cancer patient participants and refusers in observational end of life research. We hypothesized that, compared with refusers, consenters would: 1) have a stronger belief in personal gain from research participation, 2) be more satisfied with their medical care, 3) be more satisfied with support from family and friends, and 4) be in less physical discomfort compared with refusers.
METHODS: Sixty eight patients consented to enroll in the 'parent' observational study. Thirty six patients refused to participate. Reasons for refusal were recorded verbatim and coded using qualitative techniques. Both patient consenters and patient refusers were asked the same questions regarding personal gain, satisfaction with medical care, family and social support, and physical discomfort.
RESULTS: Consenters believed that they had more to gain from participation in research compared with refusers (p = 0.04). Consenters felt that aches or pain were more of a problem for them compared with refusers (p < 0.001). Both satisfaction with medical care and with support from family and friends were similar between consenters and refusers.
CONCLUSIONS: Consenting study participants in observational research at end of life believe they have more to gain from study participation than do refusers. Contrary to our hypothesis, consenting participants were those who were experiencing greater physical discomfort compared to refusers.

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Year:  2005        PMID: 15662180     DOI: 10.1089/jpm.2005.8.115

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


  4 in total

1.  Cancer-related psychosocial research: what are the perspectives of cancer care centre users on participation?

Authors:  Julie Hepworth; Ann R R Robertson; Anita Jhunjhunwala; Glyn C Jarvis; Chris McVittie
Journal:  Support Care Cancer       Date:  2010-06-20       Impact factor: 3.603

2.  Carer preferences of route of administration of transmucosal diamorphine and willingness to take part in a randomised controlled trial: an interview study (DIPPER).

Authors:  Liz Jamieson; Emily Harrop; Christina Liossi; Katherine Boyce; Lorraine Mitchell; Margaret Johnson; Yogini Jani; Victoria Akinyooye; Simon S Skene; Ian C K Wong; Richard F Howard; Kate Oulton
Journal:  BMC Palliat Care       Date:  2022-05-17       Impact factor: 3.113

3.  Perceived Benefits and Burdens of Participation for Caregivers of Cancer Patients in Hospice Clinical Trials: A Pilot Study.

Authors:  Debra Parker Oliver; Jacquelyn J Benson; Connie Ulrich; Karla T Washington; Abigail J Rolbiecki; Patrick White; Jamie B Smith; Christina Lero; Olivia J Landon; George Demiris
Journal:  J Pain Symptom Manage       Date:  2020-11-06       Impact factor: 5.576

4.  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
Journal:  BMC Med Res Methodol       Date:  2012-08-17       Impact factor: 4.615

  4 in total

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