Literature DB >> 24572010

Comparing face-to-face and online qualitative research with people with multiple sclerosis.

Anneliese Synnot1, Sophie Hill, Michael Summers, Michael Taylor.   

Abstract

We compared face-to-face focus groups and an online forum in qualitative research with people with multiple sclerosis (MS) and family members. Although the merits and challenges of online qualitative research have been considered by others, there is limited literature directly comparing these two data collection methods for people with disability or chronic illness. Twenty-seven people participated in one of four focus groups and 33 people took part in an online forum. Demographic and MS-related characteristics were similar between the two groups, with a slight nonsignificant trend toward nonmetropolitan residence in online forum participants. There was a high level of overlap in the themes generated between groups. Participant responses in the online forum were more succinct and on-topic, yet in the focus groups interaction was greater. Online qualitative research methods can facilitate research participation for people with chronic illness or disability, yielding generally comparable information to that gathered via face-to-face methods.

Entities:  

Keywords:  disability / disabled persons; focus groups; multiple sclerosis (MS); research, online; research, qualitative

Mesh:

Year:  2014        PMID: 24572010     DOI: 10.1177/1049732314523840

Source DB:  PubMed          Journal:  Qual Health Res        ISSN: 1049-7323


  7 in total

1.  Desired Resources for Changing Diet Among Persons With Multiple Sclerosis: Qualitative Inquiry Informing Future Dietary Interventions.

Authors:  Stephanie L Silveira; Emma V Richardson; Robert W Motl
Journal:  Int J MS Care       Date:  2021-10-28

2.  Developing a community-engaged wheelchair exercise program for persons with MS: community advisory board formation and feedback.

Authors:  Stephanie L Silveira; Katherine Froehlich-Grobe; Robert W Motl
Journal:  Disabil Rehabil Assist Technol       Date:  2021-12-10

3.  Online health information seeking: how people with multiple sclerosis find, assess and integrate treatment information to manage their health.

Authors:  Anneliese J Synnot; Sophie J Hill; Kerryn A Garner; Michael P Summers; Graziella Filippini; Richard H Osborne; Sue D P Shapland; Cinzia Colombo; Paola Mosconi
Journal:  Health Expect       Date:  2014-08-28       Impact factor: 3.377

4.  An Innovative Online Qualitative Study to Explore the Symptom Experience of Patients with Primary Sjögren's Syndrome.

Authors:  Kerry Gairy; Keith Ruark; Susan M Sinclair; Helen Brandwood; Linda Nelsen
Journal:  Rheumatol Ther       Date:  2020-07-28

5.  The feasibility of an online educational lifestyle program for people with multiple sclerosis: A qualitative analysis of participant semi-structured interviews.

Authors:  William Bevens; J Reece; P L Jelinek; T J Weiland; N Nag; S Simpson-Yap; K Gray; G A Jelinek; S L Neate
Journal:  Digit Health       Date:  2022-09-04

6.  Patient involvement in the development of patient-reported outcome measures: The developers' perspective.

Authors:  Bianca Wiering; Dolf de Boer; Diana Delnoij
Journal:  BMC Health Serv Res       Date:  2017-09-08       Impact factor: 2.655

7.  Online stroke forum as source of data for qualitative research: insights from a comparison with patients' interviews.

Authors:  James Jamison; Stephen Sutton; Jonathan Mant; Anna De Simoni
Journal:  BMJ Open       Date:  2018-03-30       Impact factor: 2.692

  7 in total

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