Challenges to implementing electronic trial data collection in primary care: a qualitative study
Challenges to implementing electronic trial data collection in primary care: a qualitative study
Background: Within-consultation recruitment to primary care trials is challenging. Ensuring procedures are efficient and self-explanatory is the key to optimising recruitment. Trial recruitment software that integrates with the electronic health record to support and partially automate procedures is becoming more common. If it works well, such software can support greater participation and more efficient trial designs. An innovative electronic trial recruitment and outcomes software was designed to support recruitment to the Runny Ear randomised controlled trial, comparing topical, oral and delayed antibiotic treatment for acute otitis media with discharge in children. A qualitative evaluation investigated the views and experiences of primary care staff using this trial software. Methods: Staff were purposively sampled in relation to site, role and whether the practice successfully recruited patients. In-depth interviews were conducted using a flexible topic guide, audio recorded and transcribed. Data were analysed thematically. Results: Sixteen staff were interviewed, including GPs, practice managers, information technology (IT) leads and research staff. GPs wanted trial software that automatically captures patient data. However, the experience of getting the software to work within the limited and complex IT infrastructure of primary care was frustrating and time consuming. Installation was reliant on practice level IT expertise, which varied between practices. Although most had external IT support, this rarely included supported for research IT. Arrangements for approving new software varied across practices and often, but not always, required authorisation from Clinical Commissioning Groups. Conclusions: Primary care IT systems are not solely under the control of individual practices or CCGs or the National Health Service. Rather they are part of a complex system that spans all three and is influenced by semi-autonomous stakeholders operating at different levels. This led to time consuming and sometimes insurmountable barriers to installation at the practice level. These need to be addressed if software supporting efficient research in primary care is to become a reality.
Electronic health records, Information technology, Primary health care
147
Cabral, Christie
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Curtis, Kathryn
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Curcin, Vasa
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Domínguez, Jesús
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Prasad, Vibhore
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Schilder, Anne
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Turner, Nicholas
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Wilkes, Scott
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Taylor, Jodi
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Gallagher, Sarah
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Little, Paul
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Delaney, Brendan
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Moore, Michael
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Hay, Alastair D.
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Horwood, Jeremy
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6 July 2021
Cabral, Christie
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Curtis, Kathryn
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Curcin, Vasa
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Domínguez, Jesús
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Prasad, Vibhore
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Schilder, Anne
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Turner, Nicholas
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Wilkes, Scott
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Taylor, Jodi
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Gallagher, Sarah
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Little, Paul
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Delaney, Brendan
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Moore, Michael
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Hay, Alastair D.
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Horwood, Jeremy
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Cabral, Christie, Curtis, Kathryn, Curcin, Vasa, Domínguez, Jesús, Prasad, Vibhore, Schilder, Anne, Turner, Nicholas, Wilkes, Scott, Taylor, Jodi, Gallagher, Sarah, Little, Paul, Delaney, Brendan, Moore, Michael, Hay, Alastair D. and Horwood, Jeremy
(2021)
Challenges to implementing electronic trial data collection in primary care: a qualitative study.
BMC Family Practice, 22 (1), , [147].
(doi:10.1186/s12875-021-01498-6).
Abstract
Background: Within-consultation recruitment to primary care trials is challenging. Ensuring procedures are efficient and self-explanatory is the key to optimising recruitment. Trial recruitment software that integrates with the electronic health record to support and partially automate procedures is becoming more common. If it works well, such software can support greater participation and more efficient trial designs. An innovative electronic trial recruitment and outcomes software was designed to support recruitment to the Runny Ear randomised controlled trial, comparing topical, oral and delayed antibiotic treatment for acute otitis media with discharge in children. A qualitative evaluation investigated the views and experiences of primary care staff using this trial software. Methods: Staff were purposively sampled in relation to site, role and whether the practice successfully recruited patients. In-depth interviews were conducted using a flexible topic guide, audio recorded and transcribed. Data were analysed thematically. Results: Sixteen staff were interviewed, including GPs, practice managers, information technology (IT) leads and research staff. GPs wanted trial software that automatically captures patient data. However, the experience of getting the software to work within the limited and complex IT infrastructure of primary care was frustrating and time consuming. Installation was reliant on practice level IT expertise, which varied between practices. Although most had external IT support, this rarely included supported for research IT. Arrangements for approving new software varied across practices and often, but not always, required authorisation from Clinical Commissioning Groups. Conclusions: Primary care IT systems are not solely under the control of individual practices or CCGs or the National Health Service. Rather they are part of a complex system that spans all three and is influenced by semi-autonomous stakeholders operating at different levels. This led to time consuming and sometimes insurmountable barriers to installation at the practice level. These need to be addressed if software supporting efficient research in primary care is to become a reality.
Text
Cabral 2021 Challenges REST trial quali paper
- Accepted Manuscript
More information
Accepted/In Press date: 23 June 2021
Published date: 6 July 2021
Additional Information:
Funding Information:
This research is funded by the National Institute for Health Research (NIHR) Health Technology Assessment (HTA) programme (funder ref.: 16/85/01). The views expressed in this publication are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care. The TRANSFoRm trial platform was developed as part of the EU FP7 TRANSFoRm Project 247787 ( www.transformproject.eu ). Dr Prasad received salary funding as part of the National Institute for Health Research (NIHR) academic clinical lecturer scheme, hosted by King’s College London. Other than the financial support provided, the funding body had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Funding Information:
This study was designed and delivered in collaboration with the Bristol Randomised Trials Collaboration (BRTC), part of the Bristol Trials Centre, a UKCRC registered clinical trials unit, which is in receipt of National Institute for Health Research CTU support funding. The University of Bristol is acting as sponsor for this study and is responsible for overall oversight of the trial; the NHS Bristol, North Somerset and South Gloucestershire Group (CCG) host the REST trial. The authors would like to thank all of the participants, parents, GPS and practice staff at each of the REST study sites for their involvement. The authors would like to thank all 15 UK CRNs for their role in the study. The authors would also like to thank members of their TSC and DMC.
Publisher Copyright:
© 2021, The Author(s).
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
Keywords:
Electronic health records, Information technology, Primary health care
Identifiers
Local EPrints ID: 450821
URI: http://eprints.soton.ac.uk/id/eprint/450821
ISSN: 1471-2296
PURE UUID: 61d22768-5535-402f-973b-1491cb2e500e
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Date deposited: 12 Aug 2021 16:32
Last modified: 12 Jul 2024 01:42
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Contributors
Author:
Christie Cabral
Author:
Kathryn Curtis
Author:
Vasa Curcin
Author:
Jesús Domínguez
Author:
Vibhore Prasad
Author:
Anne Schilder
Author:
Nicholas Turner
Author:
Scott Wilkes
Author:
Jodi Taylor
Author:
Sarah Gallagher
Author:
Brendan Delaney
Author:
Alastair D. Hay
Author:
Jeremy Horwood
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