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Reporting quality of clinical trial protocols: a repeated cross-sectional study about the Adherence to SPIrit Recommendations in Switzerland, CAnada and GErmany (ASPIRE-SCAGE).
Gryaznov, Dmitry; von Niederhäusern, Belinda; Speich, Benjamin; Kasenda, Benjamin; Ojeda-Ruiz, Elena; Blümle, Anette; Schandelmaier, Stefan; Mertz, Dominik; Odutayo, Ayodele; Tomonaga, Yuki; Amstutz, Alain; Pauli-Magnus, Christiane; Gloy, Viktoria; Lohner, Szimonetta; Bischoff, Karin; Wollmann, Katharina; Rehner, Laura; Meerpohl, Joerg J; Nordmann, Alain; Klatte, Katharina; Ghosh, Nilabh; Taji Heravi, Ala; Wong, Jacqueline; Chow, Ngai; Hong, Patrick; McCord-De Iaco, Kimberly A; Sricharoenchai, Sirintip; Busse, Jason W; Agarwal, Arnav; Saccilotto, Ramon; Schwenkglenks, Matthias; Moffa, Giusi; Hemkens, Lars; Hopewell, Sally; Von Elm, Erik; Briel, Matthias.
Afiliação
  • Gryaznov D; Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
  • von Niederhäusern B; Department of Clinical Research, Clinical Trial Unit, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Speich B; Roche Pharma AG, Grenzach-Wyhlen, Germany.
  • Kasenda B; Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Ojeda-Ruiz E; Oxford Clinical Trials Research Unit, Centre for Statistics in Medicine, Nuffield Department of Orthopaedics Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.
  • Blümle A; Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Schandelmaier S; Department of Medical Oncology, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Mertz D; Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Odutayo A; Preventive Medicine Department, Bioaraba Health Research Institute, Osakidetza Basque Health Service, Araba University Hospital, Vitoria-Gasteiz, Alava, Spain.
  • Tomonaga Y; Clinical Trials Unit, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.
  • Amstutz A; Cochrane Germany, Cochrane Germany Foundation, Freiburg, Germany.
  • Pauli-Magnus C; Institute for Evidence in Medicine, Medical Center, University of Freiburg, Freiburg, Germany.
  • Gloy V; Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Lohner S; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Bischoff K; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Wollmann K; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Rehner L; Oxford Clinical Trials Research Unit, Centre for Statistics in Medicine, Nuffield Department of Orthopaedics Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.
  • Meerpohl JJ; Epidemiology, Biostatistic und Prevention Institute, University of Zurich, Zurich, Switzerland.
  • Nordmann A; Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Klatte K; Clinical Research Unit, Schweizerisches Tropen- und Public Health-Institut, Basel, Switzerland.
  • Ghosh N; Department of Clinical Research, Clinical Trial Unit, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Taji Heravi A; Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Wong J; Cochrane Hungary, Clinical Centre of the University of Pécs, Medical School, University of Pécs, Pécs, Hungary.
  • Chow N; Cochrane Germany, Cochrane Germany Foundation, Freiburg, Germany.
  • Hong P; Institute for Evidence in Medicine, Medical Center, University of Freiburg, Freiburg, Germany.
  • McCord-De Iaco KA; Cochrane Germany, Cochrane Germany Foundation, Freiburg, Germany.
  • Sricharoenchai S; Institute for Evidence in Medicine, Medical Center, University of Freiburg, Freiburg, Germany.
  • Busse JW; Institute for Evidence in Medicine, Medical Center, University of Freiburg, Freiburg, Germany.
  • Agarwal A; Institute for Nursing Science and Interprofessional Learning, University Medicine Greifswald, Greifswald, Germany.
  • Saccilotto R; Cochrane Germany, Cochrane Germany Foundation, Freiburg, Germany.
  • Schwenkglenks M; Institute for Evidence in Medicine, Medical Center, University of Freiburg, Freiburg, Germany.
  • Moffa G; Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Hemkens L; Department of Clinical Research, Clinical Trial Unit, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Hopewell S; Department of Neurosurgery, University of Basel, Basel, Switzerland.
  • Von Elm E; Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Briel M; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada.
BMJ Open ; 12(5): e053417, 2022 05 24.
Article em En | MEDLINE | ID: mdl-35613804
ABSTRACT

OBJECTIVES:

Comprehensive protocols are key for the planning and conduct of randomised clinical trials (RCTs). Evidence of low reporting quality of RCT protocols led to the publication of the Standard Protocol Items Recommendations for Interventional Trials (SPIRIT) checklist in 2013. We aimed to examine the quality of reporting of RCT protocols from three countries before and after the publication of the SPIRIT checklist.

DESIGN:

Repeated cross sectional study.

SETTING:

Swiss, German and Canadian research ethics committees (RECs).

PARTICIPANTS:

RCT protocols approved by RECs in 2012 (n=257) and 2016 (n=292). PRIMARY AND SECONDARY OUTCOME

MEASURES:

The primary outcomes were the proportion of reported SPIRIT items per protocol and the proportion of trial protocols reporting individual SPIRIT items. We compared these outcomes in protocols approved in 2012 and 2016, and built regression models to explore factors associated with adherence to SPIRIT. For each protocol, we also extracted information on general trial characteristics and assessed whether individual SPIRIT items were reported

RESULTS:

The median proportion of reported SPIRIT items among RCT protocols showed a non-significant increase from 72% (IQR, 63%-79%) in 2012 to 77% (IQR, 68%-82%) in 2016. However, in a preplanned subgroup analysis, we detected a significant improvement in investigator-sponsored protocols the median proportion increased from 64% (IQR, 55%-72%) in 2012 to 76% (IQR, 64%-83%) in 2016, while for industry-sponsored protocols median adherence was 77% (IQR 72%-80%) for both years. The following trial characteristics were independently associated with lower adherence to SPIRIT single-centre trial, no support from a clinical trials unit or contract research organisation, and investigator-sponsorship.

CONCLUSIONS:

In 2012, industry-sponsored RCT protocols were reported more comprehensively than investigator-sponsored protocols. After publication of the SPIRIT checklist, investigator-sponsored protocols improved to the level of industry-sponsored protocols, which did not improve.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Comitês de Ética em Pesquisa Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: America do norte / Europa Idioma: En Revista: BMJ Open Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Comitês de Ética em Pesquisa Tipo de estudo: Clinical_trials / Guideline / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: America do norte / Europa Idioma: En Revista: BMJ Open Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suíça