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Improving the content validity of the mixed methods appraisal tool: a modified e-Delphi study.

Authors :
Hong QN
Pluye P
Fàbregues S
Bartlett G
Boardman F
Cargo M
Dagenais P
Gagnon MP
Griffiths F
Nicolau B
O'Cathain A
Rousseau MC
Vedel I
Source :
Journal of clinical epidemiology [J Clin Epidemiol] 2019 Jul; Vol. 111, pp. 49-59.e1. Date of Electronic Publication: 2019 Mar 22.
Publication Year :
2019

Abstract

Objective: The mixed methods appraisal tool (MMAT) was developed for critically appraising different study designs. This study aimed to improve the content validity of three of the five categories of studies in the MMAT by identifying relevant methodological criteria for appraising the quality of qualitative, survey, and mixed methods studies.<br />Study Design and Setting: First, we performed a literature review to identify critical appraisal tools and extract methodological criteria. Second, we conducted a two-round modified e-Delphi technique. We asked three method-specific panels of experts to rate the relevance of each criterion on a five-point Likert scale.<br />Results: A total of 383 criteria were extracted from 18 critical appraisal tools and a literature review on the quality of mixed methods studies, and 60 were retained. In the first and second rounds of the e-Delphi, 73 and 56 experts participated, respectively. Consensus was reached for six qualitative criteria, eight survey criteria, and seven mixed methods criteria. These results led to modifications of eight of the 11 MMAT (version 2011) criteria. Specifically, we reformulated two criteria, replaced four, and removed two. Moreover, we added six new criteria.<br />Conclusion: Results of this study led to improve the content validity of this tool, revise it, and propose a new version (MMAT version 2018).<br /> (Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1878-5921
Volume :
111
Database :
MEDLINE
Journal :
Journal of clinical epidemiology
Publication Type :
Academic Journal
Accession number :
30905698
Full Text :
https://doi.org/10.1016/j.jclinepi.2019.03.008