Literature DB >> 16676340

Methodological issues in the recruitment of cancer pain patients and their caregivers.

Sean Ransom1, Lora M Azzarello, Susan C McMillan.   

Abstract

Published pain management guidelines recommend that caregivers of cancer pain patients be provided pain management education, but little is known about the utility of providing such information. This study examined recruitment and retention of cancer pain patients and caregivers for a randomized clinical trial that provided psychoeducation and stress management training to caregivers. Of 397 patient/caregiver dyads screened, only 22 (5.5%) were study eligible, consented to participate, and completed the study. A variety of problems hampered successful participation, including a high proportion of non-cancer-related pain syndromes among patients, a high proportion of patients without caregivers, and participants' perception of study burden. Results suggest that researchers should recruit from a broad patient base and limit study burden on participants.

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Year:  2006        PMID: 16676340     DOI: 10.1002/nur.20129

Source DB:  PubMed          Journal:  Res Nurs Health        ISSN: 0160-6891            Impact factor:   2.228


  19 in total

1.  A noninferiority trial of a problem-solving intervention for hospice caregivers: in person versus videophone.

Authors:  George Demiris; Debra Parker Oliver; Elaine Wittenberg-Lyles; Karla Washington; Ardith Doorenbos; Tessa Rue; Donna Berry
Journal:  J Palliat Med       Date:  2012-04-26       Impact factor: 2.947

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.  Understanding recruitment and retention in neurological research.

Authors:  Alyssa Newberry; Paula Sherwood; Allison Hricik; Sarah Bradley; Jean Kuo; Elizabeth Crago; Leslie A Hoffman; Barbara A Given
Journal:  J Neurosci Nurs       Date:  2010-02       Impact factor: 1.230

4.  Feasibility of implementing an electronic social support and resource visualization tool for caregivers in a neuro-oncology clinic.

Authors:  Maija Reblin; Dana Ketcher; Peter Forsyth; Eduardo Mendivil; Lauren Kane; Justin Pok; Miriah Meyer; Yelena P Wu; Jim Agutter
Journal:  Support Care Cancer       Date:  2018-06-12       Impact factor: 3.603

5.  Recruitment of Older Adult Patient-Caregiver Dyads for an Online Caregiver Resource Program: Lessons Learned.

Authors:  Eun-Shim Nahm; Denise Orwig; Barbara Resnick; Jay Magaziner; Michele Bellantoni; Robert Sterling
Journal:  Ageing Int       Date:  2011-10-26

6.  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

7.  Family matters: examining a multi-family group intervention for women with BRCA mutations in the scope of genetic counselling.

Authors:  Alvaro Mendes; Raquel Chiquelho; Teresa Almeida Santos; Liliana Sousa
Journal:  J Community Genet       Date:  2010-10-05

8.  Circadian research in mothers and infants: how many days of actigraphy data are needed to fit cosinor parameters?

Authors:  Karen A Thomas; Robert L Burr
Journal:  J Nurs Meas       Date:  2008

9.  Research participation by older adults at end of life: barriers and solutions.

Authors:  Melissa Lehan Mackin; Keela Herr; Kimberly Bergen-Jackson; Perry Fine; Chris Forcucci; Sara Sanders
Journal:  Res Gerontol Nurs       Date:  2009-04-30       Impact factor: 1.571

10.  Factors That Impact End-of-Life Decision Making in African Americans With Advanced Cancer.

Authors:  Cathy L Campbell; Ishan C Williams; Tamara Orr
Journal:  J Hosp Palliat Nurs       Date:  2011-01-01       Impact factor: 1.918

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