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Rome Foundation Working Team Report: Consensus Statement on the Design and Conduct of Behavioural Clinical Trials for Disorders of Gut-Brain Interaction
Division of Gastroenterology, Massachusetts General Hospital, Boston, Massachusetts, USA; Harvard Medical School, Boston, Massachusetts, USA.
Division of Gastroenterology and Hepatology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA; Laboratory for Brain-Gut Axis Studies (LaBGAS), Translational Research in Gastrointestinal Disorders (TARGID), Department of Chronic Diseases and Metabolism (CHROMETA), KU Leuven, Leuven, Belgium.
Department of Biobehavioural Nursing and Health Informatics, School of Nursing, University of Washington, Seattle, Washington, USA.
Örebro University, School of Behavioural, Social and Legal Sciences. (EMBRACE Lab)ORCID iD: 0000-0003-1208-2077
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2025 (English)In: Alimentary Pharmacology and Therapeutics, ISSN 0269-2813, E-ISSN 1365-2036Article, review/survey (Refereed) Epub ahead of print
Abstract [en]

BACKGROUND: Brain-gut behaviour therapies (BGBT) have gained widespread acceptance as therapeutic modalities for the management of disorders of gut-brain interaction (DGBI). However, existing treatment evaluation methods in the medical field fail to capture the specific elements of scientific rigour unique to behavioural trial evaluation.

AIMS: To offer the first consensus on the development and testing of BGBT in DGBI.

METHODS: An international, interdisciplinary team of experts developed a consensus statement heavily informed by best practice recommendations for behavioural clinical trials for chronic diseases, organised by a selected treatment development model.

RESULTS: We suggest an existing behavioural treatment development model that has an iterative progression aligned with the drug development model with nuances specific to BGBT. We describe the iterative phases through initial discovery and experimental work, assembly of a mechanistic pathway and candidate treatment components, treatment refinement and optimisation, initial proof-of-concept, feasibility of clinical trials and, finally, confirmatory efficacy and effectiveness testing. We delineate recommendations for and provide examples that lend themselves to gastroenterologists planning to develop or test BGBT, reviewing proposals for or results from BGBT studies or writing management guidelines for DGBI.

CONCLUSIONS: This working team report facilitates a shared understanding of the elements of scientific rigour necessary for BGBT development and could support future standards on which BGBT are evaluated in gastroenterology.

Place, publisher, year, edition, pages
John Wiley & Sons, 2025.
Keywords [en]
ORBIT model, brain–gut behaviour therapy, clinical trials, disorders of gut–brain interaction, efficacy, minimum clinically important difference
National Category
Gastroenterology and Hepatology
Identifiers
URN: urn:nbn:se:oru:diva-118758DOI: 10.1111/apt.18482ISI: 001400900200001PubMedID: 39835695Scopus ID: 2-s2.0-85215388003OAI: oai:DiVA.org:oru-118758DiVA, id: diva2:1930039
Note

Funding: This work was supported by Fonds Wetenschappelijk Onderzoek (12A7822N) and National Institute of Diabetes and Digestive and Kidney Diseases (K23 DK131334 and K23 NR020044).

Available from: 2025-01-22 Created: 2025-01-22 Last updated: 2025-01-28Bibliographically approved

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