Cited by 37Inflammatory Bowel DiseaseHealth Literacy and Information AccessibilitySurvey Methodology and Nonresponse

Quality of Life in Patients With Inflammatory Bowel Disease and Irritable Bowel Syndrome Differs Between Subjects Recruited from Clinic or the Internet

Jones, Michael P., Bratten, Jason, Keefer, Laurie·2007·The American Journal of Gastroenterology

Abstract

INTRODUCTION: The Internet is used increasingly to recruit patients for studies of gastroenterological disorders. The Internet allows access to potentially large study populations but no data exist comparing Internet-based populations with patients recruited from a clinical setting. We conducted an assessment of the quality of life (QOL) in patients with active inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS) recruited from a gastroenterology clinic and the Internet. METHODS: Patients were recruited from a university gastroenterology clinic and several condition-specific support group web sites. The diagnosis of IBD and IBS was confirmed for clinic patients while Internet respondents were self-identified. Subjects completed both general (SF-36) and condition specific (IBS-QOL) measures. RESULTS: Subjects with IBD included 47 recruited from clinic and 96 recruited from the Internet. The IBS group included 147 patients recruited from clinic and 84 recruited from the Internet. Both IBS and IBD clinic and Internet IBD groups did not differ by. IBD Internet respondents were more likely to be women (clinic: 28F/19M, online: 80F/16M, P= 0.002) while IBS Internet respondents were more likely to be male (123F/24M) than IBS clinic patients (62F/22M) (P= 0.09). Compared with patients seen in clinic, both IBS and IBD Internet respondents had significantly poorer QOL as measured by both SF-36 and IBS-QOL. The greatest decrements in QOL occurred on SF-36 scales for physical and emotional roles and social functioning. On the IBS-QOL, the greatest decrement was seen on scales for dysphoria and life interference. Significant differences were maintained after controlling for gender. CONCLUSIONS: For both IBS and IBD, Internet-respondents had significantly poorer QOL than subjects recruited from clinic. These data demonstrate that subjects recruited from the Internet may represent a clinically distinct population and data obtained from online surveys may not generalize to broader clinical populations. Further study is needed to determine whether these differences reflect psychosocial characteristics of Internet responders or simply self-report behaviors in a relatively anonymous environment.

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Crossref · 10.1111/j.1572-0241.2007.01444.x

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Authors
Jones, M. P., Bratten, J., & Keefer, L.
Affiliations
Northwestern University (US)
Corresponding author
Jones, Michael P.
Venue
The American Journal of Gastroenterology
Published
2007-10
Volume
102
Issue
10
Pages
2232-2237
ISSN
  • 0002-9270 (ISSN-L)
  • 1572-0241
OpenAlex
W1989209483
Cited by
37
References
32
Citations by year
2025: 1 · 2024: 1 · 2023: 2 · 2021: 2 · 2019: 4 · 2018: 2 · 2017: 1 · 2016: 1 · 2015: 1 · 2014: 2 · 2013: 2 · 2012: 1
FWCI
2.14
Type
journal article
Language
en
Open access
closed
Locations
  • The American Journal of Gastroenterology (publishedVersion)
  • PubMed (publishedVersion)
Funders
Northwestern University
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Inflammatory Bowel Disease
  • Health Sciences › Health Professions › General Health Professions › Health Literacy and Information Accessibility
  • Social Sciences › Sociology and Political Science › Survey Methodology and Nonresponse
Keywords
quality of life, inflammatory bowel disease, irritable bowel syndrome, online recruitment, sample representativeness, SF-36, IBS-QOL, gender differences, self-report bias
MeSH terms
Adult, Ambulatory Care Facilities, Female, Health Surveys, Humans, Male, Middle Aged, Quality of Life, Self-Help Groups, Inflammatory Bowel Diseases, Patient Selection, Internet, Irritable Bowel Syndrome

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