Author
Listed:
- Ami Baba
- Maureen Smith
- Beth K Potter
(University of Ottawa [Ottawa])
- An-Wen Chan
(Ryerson University [Toronto])
- David Moher
(University of Ottawa [Ottawa], The Ottawa Hospital)
- Alene Toulany
(Ryerson University [Toronto])
- Amanda Doherty-Kirby
- Begonya Nafria Escalera
- Catherine Stratton
(Ryerson University [Toronto])
- Chris Gale
(Chelsea and Westminster Hospital)
- Colin Macarthur
- Diane Purper-Ouakil
(CESP - Centre de recherche en épidémiologie et santé des populations - UVSQ - Université de Versailles Saint-Quentin-en-Yvelines - AP-HP - Assistance publique - Hôpitaux de Paris (AP-HP) - Hôpital Paul Brousse - AP-HP. Université Paris Saclay - INSERM - Institut National de la Santé et de la Recherche Médicale - Université Paris-Saclay, Hôpital Saint Eloi [CHU Montpellier] - CHRU Montpellier - Centre Hospitalier Régional Universitaire [Montpellier])
- Edmund Juszczak
(UON - University of Nottingham, UK)
- Eyal Cohen
- Giorgio Reggiardo
(UE - Union Européenne = European Union)
- Jennifer Preston
(University of Liverpool)
- Jérémie F Cohen
(EPOPé [CRESS - U1153 / UMR_A 1125] - Obstetrical, Perinatal and Pediatric Epidemiology | Épidémiologie Obstétricale, Périnatale et Pédiatrique - CRESS (U1153 / UMR_A 1125) - Centre for Research in Epidemiology and Statistics | Centre de Recherche Épidémiologie et Statistiques - INSERM - Institut National de la Santé et de la Recherche Médicale - UPCité - Université Paris Cité - INRAE - Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement, Département de Pédiatrie et maladies infectieuses [CHU Necker] - Hôpital Necker - Enfants Malades [AP-HP] - AP-HP - Assistance publique - Hôpitaux de Paris (AP-HP))
- Julia Upton
- Karel Allegaert
(Erasmus MC - Erasmus University Medical Center [Rotterdam], KU Leuven - Catholic University of Leuven = Katholieke Universiteit Leuven)
- Katelynn Boerner
- Kayur Mehta
(JHU - Johns Hopkins University [Baltimore])
- Kim an Nguyen
(HFME - Hôpital Femme Mère Enfant [CHU - HCL] - HCL - Hospices Civils de Lyon, LBBE - Laboratoire de Biométrie et Biologie Evolutive - UMR 5558 - UCBL - Université Claude Bernard Lyon 1 - Université de Lyon - VAS - VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement - CNRS - Centre National de la Recherche Scientifique)
- Kimberly Courtney
- Lisa Hartling
(University of Alberta)
- Menelaos Konstantinidis
(Ryerson University [Toronto])
- Michal Odermarsky
- Nancy J Butcher
(Ryerson University [Toronto])
- Niina Kolehmainen
(Newcastle University [Newcastle])
- Patricia E Longmuir
- Peter J Gill
- Piet Leroy
- Reinhard Feneberg
- Ramesh Poluru
- Shaun K Morris
(Ryerson University [Toronto])
- Stefan J Friedrichsdorf
(UC San Francisco - University of California [San Francisco] - UC - University of California)
- Tanya Chute Nagy
- Terry P Klassen
(U of S - University of Saskatchewan [Saskatoon, Canada])
- Thierry Lacaze-Masmonteil
- Wes Onland
(Amsterdam UMC - Amsterdam University Medical Centers)
- Martin Offringa
Abstract
Randomised controlled trial (RCT) protocols contain essential details needed to understand and evaluate the trial's planned aims, design, data collection methods, monitoring, data analysis, and participants' safety. However, key information is often omitted from paediatric RCT protocols, including details on dose adjustments of interventions based on age, body surface area, or weight; developmental appropriateness of trial outcome measures and processes; or strategies to minimise participants' anxiety and pain. These deficiencies impair the planning and implementation of potentially impactful trials for children and adolescents. Appropriate guidance is needed to support harmonised, comprehensive reporting of paediatric RCT protocols involving participants aged 0–19 years. The methodological framework for developing reporting guidelines published by the Enhancing the Quality and Transparency of Health Research (EQUATOR) Network was implemented to develop a paediatric extension to the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) 2025 guidelines, called SPIRIT-Children and Adolescents (SPIRIT-C) 2026. A list of candidate reporting items was generated from the literature, and a Youth Advisory Group and a Family Caregiver Advisory Group contributed essential input throughout the project. An international Delphi study with a priori consensus thresholds, a consensus meeting, group writing of the explanation and elaboration paper, and pilot testing of the draft guideline were conducted. SPIRIT-C 2026 consists of a checklist with 17 new reporting items for reporting paediatric RCT protocols; four items are youth generated and six youth endorsed. SPIRIT-C 2026 can be considered a minimum set of reporting items pertinent to paediatric RCT protocols that are relevant to various interest holders, including young people, family caregivers, researchers, paediatric trialists, ethics committees, regulators, funders, and journal editors. The accompanying explanation and elaboration paper explains all items and offers examples of good reporting. Widespread implementation and uptake of SPIRIT-C 2026 should enhance the quality and usefulness of protocols for RCTs that involve participants from birth through adolescence, and ultimately foster high-quality paediatric trials.
Suggested Citation
Ami Baba & Maureen Smith & Beth K Potter & An-Wen Chan & David Moher & Alene Toulany & Amanda Doherty-Kirby & Begonya Nafria Escalera & Catherine Stratton & Chris Gale & Colin Macarthur & Diane Purper, 2026.
"SPIRIT-Children and Adolescents (SPIRIT-C) 2026 extension statement: enhancing the reporting and usefulness of paediatric randomised trial protocols,"
Post-Print
hal-05574323, HAL.
Handle:
RePEc:hal:journl:hal-05574323
DOI: 10.1016/s2352-4642(26)00005-2
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