Literature DB >> 14735681

Issues and dilemmas in conducting research with vulnerable home hospice participants.

Marjorie C Dobratz1.   

Abstract

PURPOSE: To describe issues and dilemmas related to nonparticipation, attrition, and needs for assistance in research with vulnerable home hospice participants. DESIGN AND METHODS: Retrospective analysis, with descriptive statistics of the frequency of issues and dilemmas that occurred in a research study with a vulnerable population.
FINDINGS: From a group of 113 potential participants, 16 (14.1%) people who gave initial consent were unable to participate or were lost to the study (subset I) for the following reasons: unable to give informed consent, cognitive disturbance, and physical distress. Of the 97 participants who completed testing, 28 (28.8%) required assistance (subset II) because of poor vision, physical weakness, and other physical impairments.
CONCLUSIONS: Loss of potential participants limited this study and hampered effect size. Research with home hospice patients required careful assessment for symptoms that precluded informed consent. Issues with cognition indicated need for a tool to assess mental acuity. Although several participants required assistance, those who completed testing expressed gratitude at being able to contribute information that they believed would benefit others.

Entities:  

Keywords:  Biomedical and Behavioral Research; Empirical Approach

Mesh:

Year:  2003        PMID: 14735681     DOI: 10.1111/j.1547-5069.2003.00371.x

Source DB:  PubMed          Journal:  J Nurs Scholarsh        ISSN: 1527-6546            Impact factor:   3.176


  9 in total

1.  Factors associated with attrition from a randomized controlled trial of meaning-centered group psychotherapy for patients with advanced cancer.

Authors:  Allison J Applebaum; Wendy G Lichtenthal; Hayley A Pessin; Julia N Radomski; N Simay Gökbayrak; Aviva M Katz; Barry Rosenfeld; William Breitbart
Journal:  Psychooncology       Date:  2011-07-12       Impact factor: 3.894

2.  Challenges and strategies for recruitment and retention of vulnerable research participants: promoting the benefits of participation.

Authors:  Robin Gemmill; Anna Cathy Williams; Liz Cooke; Marcia Grant
Journal:  Appl Nurs Res       Date:  2010-04-09       Impact factor: 2.257

3.  Methodological challenges in conducting a multi-site randomized clinical trial of massage therapy in hospice.

Authors:  Jean Kutner; Marlaine Smith; Karen Mellis; Sue Felton; Traci Yamashita; Lisa Corbin
Journal:  J Palliat Med       Date:  2010-06       Impact factor: 2.947

4.  Lessons from the field: challenges in accruing hospice heart failure patients to intervention research.

Authors:  Cheryl H Zambroski; Harleah Buck; Christopher M Garrison; Susan C McMillan
Journal:  J Cardiovasc Nurs       Date:  2014 Jan-Feb       Impact factor: 2.083

Review 5.  What do palliative care patients and their relatives think about research in palliative care?-a systematic review.

Authors:  Clare White; Janet Hardy
Journal:  Support Care Cancer       Date:  2009-08-25       Impact factor: 3.603

6.  Processes of consent in research for adults with impaired mental capacity nearing the end of life: systematic review and transparent expert consultation (MORECare_Capacity statement).

Authors:  C J Evans; E Yorganci; P Lewis; J Koffman; K Stone; I Tunnard; B Wee; W Bernal; M Hotopf; I J Higginson
Journal:  BMC Med       Date:  2020-07-22       Impact factor: 8.775

7.  Patient and physician perspectives on engaging in palliative and healthcare trials: a qualitative descriptive study.

Authors:  Valeria Cardenas; Anna Rahman; Jenna Giulioni; Alexis Coulourides Kogan; Susan Enguidanos
Journal:  BMC Palliat Care       Date:  2021-10-14       Impact factor: 3.234

8.  Attitudes of Homebound Older Adults and Their Caregivers Toward Research and Participation as Research Advisors.

Authors:  Ashley L Eaton England; Christine S Ritchie; Alexandria Mickler; Carla M Perissinotto; Sarah K Garrigues; Bruce Leff; Orla C Sheehan; Krista L Harrison
Journal:  Gerontologist       Date:  2021-11-15

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

  9 in total

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