Literature DB >> 24453751

Recruiting for caregiver education research: perspectives of caregivers of people with multiple sclerosis.

Katharine Preissner1, Marcia Finlayson1, Christin Henkel1.   

Abstract

Caregiver education programs can support participants in a role that is often challenging. Research is needed to determine the effectiveness of these programs; however, recruitment for such studies can be difficult. The objectives of this study were to explore 1) how multiple sclerosis (MS) caregivers respond to recruitment materials for a research study evaluating a caregiver education program, including aspects of the materials that encourage or discourage their interest in participation; and 2) what recommendations MS caregivers have for improving study recruitment advertising. Qualitative interviews were conducted with seven MS caregivers. Participants were asked about their reactions to advertisements for a pilot study intended to evaluate an MS caregiver education program. Participants were also asked to reflect on factors that would influence their decision to participate in the program and to provide suggestions to improve recruitment materials. Data were analyzed using a constant-comparative approach. Study findings indicated that the language and visual design of the advertisements influenced the participants' initial responses. Some caregivers first responded to the fact that the program was part of a research study, and these caregivers had overall negative responses to the advertising, such as concern that the program was being "tested." Other caregivers first considered the personal relevance of the program. These caregivers had neutral-to-positive responses to the flyers and weighed the relevance of the program against the research and logistical aspects. Participants provided recommendations to improve the recruitment materials. While recruiting for caregiver education research can be challenging, piloting recruitment materials and using a variety of advertising options may improve response.

Entities:  

Year:  2012        PMID: 24453751      PMCID: PMC3882986          DOI: 10.7224/1537-2073-14.4.188

Source DB:  PubMed          Journal:  Int J MS Care        ISSN: 1537-2073


  27 in total

Review 1.  Recruiting and retaining research participants for a clinical intervention study.

Authors:  J S Grant; D D DePew
Journal:  J Neurosci Nurs       Date:  1999-12       Impact factor: 1.230

2.  Neighbors, friends, and other nonkin caregivers of community-living dependent elders.

Authors:  Judith C Barker
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2002-05       Impact factor: 4.077

3.  The effectiveness of a mutual support group for family caregivers of a relative with dementia.

Authors:  Wai-Yin Fung; Wai-Tong Chien
Journal:  Arch Psychiatr Nurs       Date:  2002-06       Impact factor: 2.218

4.  The nature of care giving in a community sample of people with multiple sclerosis.

Authors:  Louise O'Hara; Lorraine De Souza; Lorely Ide
Journal:  Disabil Rehabil       Date:  2004-12-16       Impact factor: 3.033

5.  The cost of recruiting Alzheimer's disease caregivers for research.

Authors:  B A Tarlow; D F Mahoney
Journal:  J Aging Health       Date:  2000-11

6.  Factors determining participation in prevention trials among systemic lupus erythematosus patients: a qualitative study.

Authors:  Karen H Costenbader; Deborah Brome; Danielle Blanch; Victoria Gall; Elizabeth Karlson; Matthew H Liang
Journal:  Arthritis Rheum       Date:  2007-02-15

7.  A randomized controlled trial evaluating the effect of a support and education programme for spouses of people affected by stroke.

Authors:  A Franzén-Dahlin; J Larson; V Murray; R Wredling; E Billing
Journal:  Clin Rehabil       Date:  2008-08       Impact factor: 3.477

8.  Daily geographies of caregivers: mobility, routine, scale.

Authors:  Janine Wiles
Journal:  Soc Sci Med       Date:  2003-10       Impact factor: 4.634

9.  The experience of spousal carers of people with multiple sclerosis.

Authors:  Jenny Cheung; Peta Hocking
Journal:  Qual Health Res       Date:  2004-02

Review 10.  The needs and experiences of caregivers of individuals with multiple sclerosis: a systematic review.

Authors:  L P McKeown; A P Porter-Armstrong; G D Baxter
Journal:  Clin Rehabil       Date:  2003-05       Impact factor: 3.477

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  2 in total

Review 1.  Left Ventricular Assist Device Caregiver Experiences and Health Outcomes: A Systematic Review of Qualitative and Quantitative Studies.

Authors:  Megan M Streur; Jonathan P Auld; Ana Carolina Sauer Liberato; Jennifer A Beckman; Claudius Mahr; Elaine A Thompson; Cynthia M Dougherty
Journal:  J Card Fail       Date:  2020-06-05       Impact factor: 5.712

2.  Identifying Family and Unpaid Caregivers in Electronic Health Records: Descriptive Analysis.

Authors:  Jessica E Ma; Janet Grubber; Cynthia J Coffman; Virginia Wang; S Nicole Hastings; Kelli D Allen; Megan Shepherd-Banigan; Kasey Decosimo; Joshua Dadolf; Caitlin Sullivan; Nina R Sperber; Courtney H Van Houtven
Journal:  JMIR Form Res       Date:  2022-07-18
  2 in total

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