Literature DB >> 25741529

Improving a Case-Control Study of Multiple Sclerosis Using Formative Research.

Dhelia M Williamson1, Laurie Wagner2, Judy P Henry3.   

Abstract

Formative research (i.e. focus groups and key informant interviews) was conducted to understand risk perceptions and identify barriers to participation in a case-control study of environmental exposures and genetic susceptibility as risk factors for multiple sclerosis (MS). Individuals with MS were recruited to participate in a focus group discussion and individual interviews. Participants were asked to review and comment on study materials and process including participation, interview, genetic testing, confidentiality, and questionnaire. A structured discussion guide was used with all participants to ensure uniformity and coverage of all predetermined topics. Participants reported an increased likelihood of participation if they were informed about the study by their neurologist and not a government agency. All participants expressed willingness to provide a blood sample for genotyping but disagreed about the setting for the blood draw (at home or in a lab). Participants were concerned that they would not receive their individual genotyping results. The study protocol and materials were revised based on comments from the focus group participants. Formative research is an under-utilized resource for researchers conducting epidemiologic studies. Even with limited resources, piloting study materials with individuals similar to the proposed study population can provide opportunities to make modifications to effectively meet the needs of participants and promote participation and retention.

Entities:  

Keywords:  Case-Control Study; Environmental Risk Factors; Formative Research; Genetic Susceptibility; Multiple Sclerosis

Year:  2013        PMID: 25741529      PMCID: PMC4331063          DOI: 10.13189/ujph.2013.010406

Source DB:  PubMed          Journal:  Univers J Public Health        ISSN: 2331-8880


  12 in total

Review 1.  Genetic test evaluation: information needs of clinicians, policy makers, and the public.

Authors:  Wylie Burke; David Atkins; Marta Gwinn; Alan Guttmacher; James Haddow; Joseph Lau; Glenn Palomaki; Nancy Press; C Sue Richards; Louise Wideroff; Georgia L Wiesner
Journal:  Am J Epidemiol       Date:  2002-08-15       Impact factor: 4.897

2.  Design, methodological issues and participation in a multiple sclerosis case-control study.

Authors:  D M Williamson; R A Marrie; A Ashley-Koch; R Schiffer; J Trottier; L Wagner
Journal:  Acta Neurol Scand       Date:  2011-12-16       Impact factor: 3.209

3.  Attitudes about genetics in underserved, culturally diverse populations.

Authors:  Diana S Catz; Nancy S Green; Jonathan N Tobin; Michele A Lloyd-Puryear; Penny Kyler; Ann Umemoto; Jennifer Cernoch; Roxane Brown; Fredericka Wolman
Journal:  Community Genet       Date:  2005

4.  Formative research in school and community-based health programs and studies: "state of the art" and the TAAG approach.

Authors:  Joel Gittelsohn; Allan Steckler; Carolyn C Johnson; Charlotte Pratt; Mira Grieser; Julie Pickrel; Elaine J Stone; Terry Conway; Derek Coombs; Lisa K Staten
Journal:  Health Educ Behav       Date:  2006-02

Review 5.  Use of focus groups for the environmental health researcher.

Authors:  Danelle T Lobdell; Suzanne Gilboa; Pauline Mendola; Bradford W Hesse
Journal:  J Environ Health       Date:  2005-05       Impact factor: 1.179

6.  Investigation of a cluster of multiple sclerosis in two elementary school cohorts.

Authors:  Judy P Henry; Dhelia M Williamson; Randolph Schiffer; Laurie Wagner; Jeffrey Shire; Matthew Garabedian
Journal:  J Environ Health       Date:  2007-06       Impact factor: 1.179

Review 7.  Encouraging participation in medical research: what strategies work?

Authors:  Lindsay M Morton
Journal:  J Clin Epidemiol       Date:  2008-03-21       Impact factor: 6.437

8.  Public perspectives on returning genetics and genomics research results.

Authors:  J O'Daniel; S B Haga
Journal:  Public Health Genomics       Date:  2011-05-07       Impact factor: 2.000

9.  Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study.

Authors:  Samantha A Streicher; Saskia C Sanderson; Ethylin Wang Jabs; Michael Diefenbach; Meg Smirnoff; Inga Peter; Carol R Horowitz; Barbara Brenner; Lynne D Richardson
Journal:  J Community Genet       Date:  2011-06-07

10.  Focus group approach for developing written patient information in oncogenetics.

Authors:  Christine Lasset; Marie Charavel; Valérie Bonadona
Journal:  Genet Test       Date:  2007
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.