Guidelines for Reporting Outcomes in Trial Protocols: The SPIRIT-Outcomes 2022 Extension.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
20 12 2022
Historique:
pubmed: 14 12 2022
medline: 23 12 2022
entrez: 13 12 2022
Statut: ppublish

Résumé

Complete information in a trial protocol regarding study outcomes is crucial for obtaining regulatory approvals, ensuring standardized trial conduct, reducing research waste, and providing transparency of methods to facilitate trial replication, critical appraisal, accurate reporting and interpretation of trial results, and knowledge synthesis. However, recommendations on what outcome-specific information should be included are diverse and inconsistent. To improve reporting practices promoting transparent and reproducible outcome selection, assessment, and analysis, a need for specific and harmonized guidance as to what outcome-specific information should be addressed in clinical trial protocols exists. To develop harmonized, evidence- and consensus-based standards for describing outcomes in clinical trial protocols through integration with the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) 2013 statement. Using the Enhancing the Quality and Transparency of Health Research (EQUATOR) methodological framework, the SPIRIT-Outcomes 2022 extension of the SPIRIT 2013 statement was developed by (1) generation and evaluation of candidate outcome reporting items via consultation with experts and a scoping review of existing guidance for reporting trial outcomes (published within the 10 years prior to March 19, 2018) identified through expert solicitation, electronic database searches of MEDLINE and the Cochrane Methodology Register, gray literature searches, and reference list searches; (2) a 3-round international Delphi voting process (November 2018-February 2019) completed by 124 panelists from 22 countries to rate and identify additional items; and (3) an in-person consensus meeting (April 9-10, 2019) attended by 25 panelists to identify essential items for outcome-specific reporting to be addressed in clinical trial protocols. The scoping review and consultation with experts identified 108 recommendations relevant to outcome-specific reporting to be addressed in trial protocols, the majority (72%) of which were not included in the SPIRIT 2013 statement. All recommendations were consolidated into 56 items for Delphi voting; after the Delphi survey process, 19 items met criteria for further evaluation at the consensus meeting and possible inclusion in the SPIRIT-Outcomes 2022 extension. The discussions during and after the consensus meeting yielded 9 items that elaborate on the SPIRIT 2013 statement checklist items and are related to completely defining and justifying the choice of primary, secondary, and other outcomes (SPIRIT 2013 statement checklist item 12) prospectively in the trial protocol, defining and justifying the target difference between treatment groups for the primary outcome used in the sample size calculations (SPIRIT 2013 statement checklist item 14), describing the responsiveness of the study instruments used to assess the outcome and providing details on the outcome assessors (SPIRIT 2013 statement checklist item 18a), and describing any planned methods to account for multiplicity relating to the analyses or interpretation of the results (SPIRIT 2013 statement checklist item 20a). This SPIRIT-Outcomes 2022 extension of the SPIRIT 2013 statement provides 9 outcome-specific items that should be addressed in all trial protocols and may help increase trial utility, replicability, and transparency and may minimize the risk of selective nonreporting of trial results.

Identifiants

pubmed: 36512367
pii: 2799547
doi: 10.1001/jama.2022.21243
doi:

Types de publication

Journal Article Practice Guideline Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2345-2356

Subventions

Organisme : Medical Research Council
ID : MR/S014357/1
Pays : United Kingdom
Organisme : CIHR
Pays : Canada

Auteurs

Nancy J Butcher (NJ)

Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.
Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.

Andrea Monsour (A)

Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.

Emma J Mew (EJ)

Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.
Department of Chronic Disease Epidemiology, School of Public Health, Yale University, New Haven, Connecticut.

An-Wen Chan (AW)

Department of Medicine, Women's College Research Institute, University of Toronto, Toronto, Ontario, Canada.

David Moher (D)

Centre for Journalology, Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.

Evan Mayo-Wilson (E)

Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill.

Caroline B Terwee (CB)

Amsterdam University Medical Centers, Vrije Universiteit, Department of Epidemiology and Data Science, Amsterdam, the Netherlands.
Department of Methodology, Amsterdam Public Health Research Institute, Amsterdam, the Netherlands.

Alyssandra Chee-A-Tow (A)

Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.

Ami Baba (A)

Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.

Frank Gavin (F)

public panel member, Toronto, Ontario, Canada.

Jeremy M Grimshaw (JM)

Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Lauren E Kelly (LE)

Department of Pharmacology and Therapeutics, University of Manitoba, Winnipeg, Canada.
Children's Hospital Research Institute of Manitoba, Winnipeg, Canada.

Leena Saeed (L)

Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.

Lehana Thabane (L)

Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada.

Lisa Askie (L)

NHMRC Clinical Trials Centre, University of Sydney, Sydney, New South Wales, Australia.

Maureen Smith (M)

patient panel member, Ottawa, Ontario, Canada.

Mufiza Farid-Kapadia (M)

Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.

Paula R Williamson (PR)

MRC-NIHR Trials Methodology Research Partnership, Department of Health Data Science, University of Liverpool, Liverpool, England.

Peter Szatmari (P)

Cundill Centre for Child and Youth Depression, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Department of Psychiatry, The Hospital for Sick Children, Toronto, Ontario, Canada.

Peter Tugwell (P)

School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.
Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Bruyère Research Institute, Ottawa, Ontario, Canada.
Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

Robert M Golub (RM)

Department of Medicine, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.

Suneeta Monga (S)

Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.
Department of Psychiatry, The Hospital for Sick Children, Toronto, Ontario, Canada.

Sunita Vohra (S)

Departments of Pediatrics and Psychiatry, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada.

Susan Marlin (S)

Clinical Trials Ontario, Toronto, Canada.
Department of Public Health Sciences, Queen's University, Kingston, Ontario, Canada.

Wendy J Ungar (WJ)

Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.
Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada.

Martin Offringa (M)

Child Health Evaluative Sciences, The Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.
Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada.
Division of Neonatology, The Hospital for Sick Children, Toronto, Ontario, Canada.

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