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The contributor roles for randomized controlled trials and the proposal for a novel CRediT-RCT
Zhongheng Zhang1, Stephen D Wang2, Grace S Li2
1Department of Emergency Medicine, Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou 310016, China.
This study analyzed the Contributor Roles Taxonomy (CRediT) in randomized controlled trials (RCTs), finding common roles like conceptualization and investigation but limited software management. A new CRediT-RCT taxonomy is proposed for better role definition in clinical trials.
Area of Science:
- Bibliometrics
- Scientific Publishing
- Clinical Trials
Background:
- Increasing author numbers necessitate clear role definitions.
- The Contributor Roles Taxonomy (CRediT) aims to define author contributions.
- Empirical data on CRediT usage in clinical trials is lacking.
Purpose of the Study:
- To provide empirical data on CRediT application in randomized controlled trials (RCTs).
- To identify limitations of the current CRediT taxonomy for RCTs.
- To propose an improved taxonomy, CRediT-RCT, for defining author roles in RCTs.
Main Methods:
- PubMed database search for RCTs (July 2017 - October 2019).
- Inclusion of Public Library of Science (PLoS) publications for embedded CRediT metadata.
- Analysis of author roles and their correlations within included RCTs.
Main Results:
- 446 articles and 4,185 authors analyzed.
- Conceptualization (44.9%) and investigation (48.8%) were most common author roles.
- Funding acquisition, project administration, supervision, and original draft writing were associated with corresponding authorship.
- First authors were strongly associated with original draft writing but less with review, editing, or supervision.
Conclusions:
- The study offers empirical insights into CRediT use in RCTs.
- Limitations of the existing CRediT taxonomy for clinical trials were identified.
- A new taxonomy, CRediT-RCT, with 10 roles is proposed to enhance author role clarity in RCTs.
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