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Use of Template Documents with Guidance to Improve the Quality of Human Subjects Research Protocol Submissions to a Thai Research Ethics Committee.

Authors
  • Khawcharoenporn, Thana1, 2
  • Chimkhong, Wilaiwan2
  • Roestpricha, Varanya2
  • 1 Department of Internal Medicine, Faculty of Medicine, 37699Thammasat University, Pathumthani, Thailand. , (Thailand)
  • 2 Human Research Ethics Committee of Thammasat University (Medicine), 37699Thammasat University, Pathumthani, Thailand. , (Thailand)
Type
Published Article
Journal
Journal of empirical research on human research ethics : JERHRE
Publication Date
Dec 01, 2021
Volume
16
Issue
5
Pages
501–513
Identifiers
DOI: 10.1177/15562646211025470
PMID: 34125621
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

A pre-post study was conducted to evaluate the utility of template documents specifically created to assist research protocol submissions to a Thai research ethics committee (REC). A total of 172 protocols during the 2014-2016 preintervention period were matched to 172 protocols during the 2017-2019 postintervention period by type of principal investigator and REC review category. The intervention was associated with a significant reduction in initial REC requirement deficiencies in the information sheet and informed consent form, resubmission turn-around time by the principal investigator, and time form protocol submission to REC approval. The most significant postintervention improvements were for information about the consent process and listed risks of study participation. In this study, utilization of a structured protocol template with guidance instructions was associated with measurable improvement in the quality of research protocol submissions and REC review process.

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