2023
DOI: 10.12688/hrbopenres.13667.1
|View full text |Cite
|
Sign up to set email alerts
|

Qualitative data sharing practices in clinical trials in the UK and Ireland: towards the production of good practice guidance

Abstract: Background: Data sharing enables researchers to conduct novel research with previously collected datasets, thus maximising scientific findings and cost effectiveness, and reducing research waste. The value of sharing, even de-identified, quantitative data from clinical trials is well recognised with a moderated access approach recommended. While substantial challenges to sharing quantitative data remain, there are additional challenges for sharing qualitative data in trials. Incorporating the necessary informa… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
2

Relationship

2
0

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 38 publications
0
2
0
Order By: Relevance
“…Qualitative research alongside RCTs provides added value [ 71 , 72 ]. In our study, qualitative research, particularly in the process evaluation, helped provide an in-depth account of men’s experiences of participating as well as researchers’ experiences of delivering the interventions.…”
Section: Discussionmentioning
confidence: 99%
“…Qualitative research alongside RCTs provides added value [ 71 , 72 ]. In our study, qualitative research, particularly in the process evaluation, helped provide an in-depth account of men’s experiences of participating as well as researchers’ experiences of delivering the interventions.…”
Section: Discussionmentioning
confidence: 99%
“…[47,61]). There are currently very few examples of cross-trial qualitative data analysis undertaken by unconnected research teams likely due to the additional barriers that data sharing of this nature presents [62]. Although several researchers within the MRC-NIHR TMRP expressed an interest in collaborating, and they had patient consent to share data, opportunities to collaborate were limited as most researchers had not collected/retained data on certain patient socio-demographics, such as socioeconomic status.…”
Section: Strengths and Weaknessesmentioning
confidence: 99%