2015
DOI: 10.1186/s12916-015-0532-z
|View full text |Cite
|
Sign up to set email alerts
|

How should individual participant data (IPD) from publicly funded clinical trials be shared?

Abstract: BackgroundIndividual participant data (IPD) from completed clinical trials should be responsibly shared to support efficient clinical research, generate new knowledge and bring benefit to patients. The Medical Research Council (MRC) Hubs for Trials Methodology Research (HTMR) has developed guidance to facilitate the sharing of IPD from publicly funded clinical trials.MethodsDevelopment of the guidance was completed over four phases which included a focussed review of policy documents, a web-based survey of the… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
45
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 50 publications
(47 citation statements)
references
References 19 publications
2
45
0
Order By: Relevance
“…Although specific consent for data sharing was not obtained, the management group will consider the release of data on a case-by-case basis following published guidelines. 195 The presented data do not contain any direct identifiers; we will minimise indirect identifiers and remove free-text data to minimise the risk of identification.…”
Section: Data Sharing Statementmentioning
confidence: 99%
“…Although specific consent for data sharing was not obtained, the management group will consider the release of data on a case-by-case basis following published guidelines. 195 The presented data do not contain any direct identifiers; we will minimise indirect identifiers and remove free-text data to minimise the risk of identification.…”
Section: Data Sharing Statementmentioning
confidence: 99%
“…Various key players are taking initiatives, holding discussions, producing statements and declaring policies regarding research data sharing ( 17 19 ). Many have contributed substantially to its increase, including the ICMJE, Ottawa statement, WHO, Cochrane, Declaration of Helsinki, the REWARD (REduce research Waste And Reward Diligence) Campaign, the Institute of Medicine report (IOM), and the AllTrials initiative ( 14 , 20 - 25 ).…”
Section: Resultsmentioning
confidence: 99%
“…Although specific consent for data sharing was not obtained, the management group will consider the release of data on a case-by-case basis following published guidelines. 278 The data presented do not contain any direct identifiers; we shall minimise indirect identifiers and remove free-text data to minimise the risk of identification. This protocol amendment was in relation to the following: it was clarified that the 6MWD should be completed only once at baseline and 26 weeks.…”
Section: Costs Borne By Patientsmentioning
confidence: 99%