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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
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Kwakkenbos Aug 2018.pdf | Published version | 182.2 kB | Adobe PDF | View/Open |
Title: | Protocol for a scoping review to support development of a CONSORT extension for randomised controlled trials using cohorts and routinely collected health data |
Authors: | Kwakkenbos, L Imran, M McCord, K Sampson, M Fröbert, O Gale, C Hemkens, L Langan, S Moher, D Relton, C Zwarenstein, M Benchimol, E Boutron, I Campbell, M Erlinge, D Jawad, S Ravaud, P Rice, D Sauve, M Van Staa, T Thabane, L Uher, R Verkooijen, H Juszczak, E Thombs, B |
Item Type: | Journal Article |
Abstract: | 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. |
Issue Date: | 5-Aug-2018 |
Date of Acceptance: | 12-Jul-2018 |
URI: | http://hdl.handle.net/10044/1/62699 |
DOI: | https://dx.doi.org/10.1136/bmjopen-2018-025266 |
ISSN: | 2044-6055 |
Publisher: | BMJ Journals |
Journal / Book Title: | BMJ Open |
Volume: | 8 |
Issue: | 8 |
Copyright Statement: | © Author(s) (or their employer(s)) 2018. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
Sponsor/Funder: | National Institute of Health Research Canadian Institutes of Health Research |
Funder's Grant Number: | NIHR Clinical Trials Unit Support Funding 389515 |
Keywords: | cohort consort randomized controlled trials rcts reporting guideline routinely collected health data |
Publication Status: | Published |
Article Number: | ARTN e025266 |
Online Publication Date: | 2018-08-05 |
Appears in Collections: | Department of Medicine (up to 2019) |