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Protocol for a scoping review to support development of a CONSORT extension for randomised controlled trials using cohorts and routinely collected health data.
Kwakkenbos, Linda; Imran, Mahrukh; McCord, Kimberly A; Sampson, Margaret; Fröbert, Ole; Gale, Chris; Hemkens, Lars G; Langan, Sinead M; Moher, David; Relton, Clare; Zwarenstein, Merrick; Benchimol, Eric I; Boutron, Isabelle; Campbell, Marion K; Erlinge, David; Jawad, Sena; Ravaud, Philippe; Rice, Danielle B; Sauve, Maureen; van Staa, Tjeerd P; Thabane, Lehana; Uher, Rudolf; Verkooijen, Helena M; Juszczak, Edmund; Thombs, Brett D.
Affiliation
  • Kwakkenbos L; Behavioural Science Institute, Clinical Psychology, Radboud University, Nijmegen, Gelderland, Netherlands.
  • Imran M; Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Quebec, Canada.
  • McCord KA; Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel, University of Basel, Basel, Switzerland.
  • Sampson M; Library Services, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Fröbert O; Department of Cardiology, Faculty of Health, Örebro University, Örebro, UK.
  • Gale C; Section of Neonatal Medicine, Department of Medicine, Imperial College London, London, UK.
  • Hemkens LG; Basel Institute for Clinical Epidemiology and Biostatistics, Department of Clinical Research, University Hospital Basel, University of Basel, Basel, Switzerland.
  • Langan SM; Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK.
  • Moher D; Centre for Journalology, Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • Relton C; Centre for Clinical Trials and Methodology, Barts Institute of Population Health Science, Queen Mary University, London, UK.
  • Zwarenstein M; Department of Family Medicine, Western University, London, UK.
  • Benchimol EI; Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.
  • Boutron I; Department of Pediatrics and School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.
  • Campbell MK; Institute for Clinical Evaluative Sciences, Ottawa, Ontario, Canada.
  • Erlinge D; Division of Gastroenterology, Hepatology and Nutrition, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
  • Jawad S; Sorbonne Paris Cité Epidemiology and Statistics Research Center, INSERM, UMR1153, Paris, France.
  • Ravaud P; Centre d'Épidémiologie Clinique, Hôpital Hôtel Dieu, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Rice DB; Faculté de Médecine, Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
  • Sauve M; Health Services Research Unit, University of Aberdeen, Aberdeen, UK.
  • van Staa TP; Department of Cardiology, Clinical Sciences, Lund University, Lund, Sweden.
  • Thabane L; Section of Neonatal Medicine, Department of Medicine, Imperial College London, London, UK.
  • Uher R; Sorbonne Paris Cité Epidemiology and Statistics Research Center, INSERM, UMR1153, Paris, France.
  • Verkooijen HM; Centre d'Épidémiologie Clinique, Hôpital Hôtel Dieu, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Juszczak E; Faculté de Médecine, Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
  • Thombs BD; Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Quebec, Canada.
BMJ Open ; 8(8): e025266, 2018 08 05.
Article in En | MEDLINE | ID: mdl-30082372
INTRODUCTION: Randomised controlled trials (RCTs) conducted using cohorts and routinely collected health data, including registries, electronic health records and administrative databases, are increasingly used in healthcare intervention research. The development of an extension of the CONsolidated Standards of Reporting Trials (CONSORT) statement for RCTs using cohorts and routinely collected health data is being undertaken with the goal of improving reporting quality by setting standards early in the process of uptake of these designs. To develop this extension to the CONSORT statement, a scoping review will be conducted to identify potential modifications or clarifications of existing reporting guideline items, as well as additional items needed for reporting RCTs using cohorts and routinely collected health data. METHODS AND ANALYSIS: In separate searches, we will seek publications on methods or reporting or that describe protocols or results from RCTs using cohorts, registries, electronic health records and administrative databases. Data sources will include Medline and the Cochrane Methodology Register. For each of the four main types of RCTs using cohorts and routinely collected health data, separately, two investigators will independently review included publications to extract potential checklist items. A potential item will either modify an existing CONSORT 2010, Strengthening the Reporting of Observational Studies in Epidemiology or REporting of studies Conducted using Observational Routinely collected health Data item or will be proposed as a new item. Additionally, we will identify examples of good reporting in RCTs using cohorts and routinely collected health data. ETHICS AND DISSEMINATION: The proposed scoping review will help guide the development of the CONSORT extension statement for RCTs conducted using cohorts and routinely collected health data.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Research Design / Randomized Controlled Trials as Topic / Cohort Studies / Guidelines as Topic Type of study: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Aspects: Ethics Limits: Humans Language: En Journal: BMJ Open Year: 2018 Document type: Article Affiliation country: Países Bajos Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Research Design / Randomized Controlled Trials as Topic / Cohort Studies / Guidelines as Topic Type of study: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Aspects: Ethics Limits: Humans Language: En Journal: BMJ Open Year: 2018 Document type: Article Affiliation country: Países Bajos Country of publication: Reino Unido