Improving the capture and reporting of adverse events in clinical trials of non-pharmacological interventions: learnings from the PaCCSC/CST membership

Abstract Background Accurate capture and reporting of adverse events (AEs) in clinical trials is critical to understanding the potential harms of prospective interventions. Current AE-reporting frameworks are specifically constructed for pharmacological interventions and adaptation of these framewor...

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Bibliographic Details

Published in:	Trials
Main Authors:	Rayan Saleh Moussa, Jack Power, Vanessa Yenson, Belinda Fazekas, Celia Marston, Annmarie Hosie, Layla Edwards, Domenica Disalvo, Linda Brown, Imelda Gilmore, John Stubbs, Andrea Cross, Sally Fielding, Meera R. Agar
Format:	Article
Language:	English
Published:	BMC 2025-03-01
Subjects:	Adverse events Non-pharmacological Risk management Clinical trials Intervention Harm
Online Access:	https://doi.org/10.1186/s13063-025-08801-1