Can learnings from the COVID-19 pandemic improve trial conduct post-pandemic? A case study of strategies used by the DISC trial.

COVID-19 Randomised controlled trial dupuytren’s intervention delivery pandemic recruitment retention trial management

Journal

Research methods in medicine & health sciences
ISSN: 2632-0843
Titre abrégé: Res Methods Med Health Sci
Pays: United States
ID NLM: 9918300979306676

Informations de publication

Date de publication:
Mar 2023
Historique:
medline: 1 3 2023
pubmed: 1 3 2023
entrez: 11 4 2024
Statut: ppublish

Résumé

RCTs often face issues such as slow recruitment, poor intervention adherence and high attrition, however the 2020/2021 COVID-19 pandemic intensified these challenges. Strategies employed by the DISC trial to overcome pandemic-related barriers to recruitment, treatment delivery and retention may be useful to help overcome routine problems. A structured survey and teleconference with sites was undertaken. Key performance indicators in relation to recruitment, treatment delivery and retention were compared descriptively before and after the pandemic started. This was situated also in relation to qualitative opinions of research staff. Prior to the pandemic, retention was 93.6%. Increased support from the central trial management team and remote data collection methods kept retention rates high at 81.2% in the first 6 months of the pandemic, rising to 89.8% in the subsequent 6 months. Advertising the study to patients resulted in 12.8 patients/month enquiring about participation, however only six were referred to recruiting sites. Sites reported increased support from junior doctors resolved research nurse capacity issues. One site avoided long delays by using theatre space in a private hospital. Recruitment post-pandemic could be improved by identification of barriers, increased support from junior doctors through the NIHR associate PI scheme and advertising. Remote back-up options for data collection can keep retention high while reducing patient and site burden. To future proof studies against similar disruptions and provide more flexibility for participants, we recommend that RCTs have a back-up option of remote recruitment, a back-up location for surgeries and flexible approaches to collecting data.

Sections du résumé

Background UNASSIGNED
RCTs often face issues such as slow recruitment, poor intervention adherence and high attrition, however the 2020/2021 COVID-19 pandemic intensified these challenges. Strategies employed by the DISC trial to overcome pandemic-related barriers to recruitment, treatment delivery and retention may be useful to help overcome routine problems.
Methods UNASSIGNED
A structured survey and teleconference with sites was undertaken. Key performance indicators in relation to recruitment, treatment delivery and retention were compared descriptively before and after the pandemic started. This was situated also in relation to qualitative opinions of research staff.
Results UNASSIGNED
Prior to the pandemic, retention was 93.6%. Increased support from the central trial management team and remote data collection methods kept retention rates high at 81.2% in the first 6 months of the pandemic, rising to 89.8% in the subsequent 6 months. Advertising the study to patients resulted in 12.8 patients/month enquiring about participation, however only six were referred to recruiting sites. Sites reported increased support from junior doctors resolved research nurse capacity issues. One site avoided long delays by using theatre space in a private hospital.
Conclusions UNASSIGNED
Recruitment post-pandemic could be improved by identification of barriers, increased support from junior doctors through the NIHR associate PI scheme and advertising. Remote back-up options for data collection can keep retention high while reducing patient and site burden. To future proof studies against similar disruptions and provide more flexibility for participants, we recommend that RCTs have a back-up option of remote recruitment, a back-up location for surgeries and flexible approaches to collecting data.

Identifiants

pubmed: 38603296
doi: 10.1177/26320843221128296
pii: 10.1177_26320843221128296
pmc: PMC9500425
doi:

Types de publication

Journal Article

Langues

eng

Pagination

50-60

Informations de copyright

© The Author(s) 2022.

Déclaration de conflit d'intérêts

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

Catherine Knowlson (C)

Department of Health Sciences, York Trials Unit, York, UK.

Puvan Tharmanathan (P)

Department of Health Sciences, York Trials Unit, York, UK.

Catherine Arundel (C)

Department of Health Sciences, York Trials Unit, York, UK.

Sophie James (S)

Department of Health Sciences, York Trials Unit, York, UK.

Lydia Flett (L)

Department of Health Sciences, York Trials Unit, York, UK.

Samantha Gascoyne (S)

Department of Health Sciences, York Trials Unit, York, UK.

Charlie Welch (C)

Department of Health Sciences, York Trials Unit, York, UK.

David Warwick (D)

University Hospital Southampton, York, UK.

Joseph Dias (J)

University Hospitals of Leicester NHS Trust, York, UK.

Classifications MeSH