Skip to main content
Top
Published in: Trials 1/2019

Open Access 01-12-2019 | Methodology

A review of current practice in the design and assessment of internal pilots in UK NIHR clinical trials

Authors: Anna Rosala-Hallas, Carrol Gamble, Jane Blazeby, Paula R. Williamson

Published in: Trials | Issue 1/2019

Login to get access

Abstract

Background

Internal pilots provide useful information which can help to optimise the running of the main trial. Although some recommendations exist in the literature for the design of internal pilots, little is known about current practice in terms of the specification and also the assessment of progression criteria. The aim of the review is to provide an overview of current practice.

Methods

A cohort of clinical trials with an internal pilot, funded by the National Institute for Health Research (NIHR), Health Technology Assessment programme (HTA), extracted in 2017 was reviewed. Data were extracted from: project descriptions; summary of changes from the first stage; feedback about the full application; monitoring notes; progress report history and protocols, for information about the design and assessment of internal pilots.

Results

Fifty-seven studies were reviewed. An internal pilot was first proposed in the early stages of the trial in the majority of cases. Target number for recruitment, rate of randomisation, retention/primary outcome ascertainment rate, rate of treatment adherence and consent rate were included as progression criteria. All but one study was permitted to continue to the main trial; however, 25% did not strictly meet the progression criteria. Changes were made to the design of the main trial for 25% of studies, mainly in terms of conduct of recruitment.

Conclusions

This review provides insight into the process of designing and assessing internal pilots. Progression criteria are sometimes not met; however, committees involved in the reviewing process will recommend continuation to the main trial, usually accompanied by a second review or close monitoring. Recommendations are made to optimise the process.
Appendix
Available only for authorised users
Literature
1.
go back to reference Blatch-Jones AJ, Pek W, Kirkpatrick E, Ashton-Key M. Role of feasibility and pilot studies in randomised controlled trials: a cross-sectional study. BMJ Open. 2018;8:e022233.CrossRef Blatch-Jones AJ, Pek W, Kirkpatrick E, Ashton-Key M. Role of feasibility and pilot studies in randomised controlled trials: a cross-sectional study. BMJ Open. 2018;8:e022233.CrossRef
2.
go back to reference Lancaster GA, Dodd S, Williamson PR. Design and analysis of pilot studies: recommendations for good practice. J Eval Clin Pract. 2004;10:307–12.CrossRef Lancaster GA, Dodd S, Williamson PR. Design and analysis of pilot studies: recommendations for good practice. J Eval Clin Pract. 2004;10:307–12.CrossRef
4.
go back to reference Avery KN, Williamson PR, Gamble C, O’Connell Francischetto E, Metcalfe C, Davidson P, Williams H, Blazeby JM. members of the Internal Pilot Trials Workshop supported by the Hubs for Trials Methodology Research. Informing efficient randomised controlled trials: exploration of challenges in developing progression criteria for internal pilot studies. BMJ Open. 2017;7:e013537.CrossRef Avery KN, Williamson PR, Gamble C, O’Connell Francischetto E, Metcalfe C, Davidson P, Williams H, Blazeby JM. members of the Internal Pilot Trials Workshop supported by the Hubs for Trials Methodology Research. Informing efficient randomised controlled trials: exploration of challenges in developing progression criteria for internal pilot studies. BMJ Open. 2017;7:e013537.CrossRef
5.
go back to reference Hampson LV, Williamson PR, Wilby MJ, Jaki T. A framework for prospectively defining progression rules for internal pilot studies monitoring recruitment. Stat Methods Med Res. 2018;27:3612–27.CrossRef Hampson LV, Williamson PR, Wilby MJ, Jaki T. A framework for prospectively defining progression rules for internal pilot studies monitoring recruitment. Stat Methods Med Res. 2018;27:3612–27.CrossRef
7.
go back to reference Eldridge SM, Chan CL, Campbell MJ, Bond CM, Hopewell S, Thabane L, Lancaster GA, PAFS Consensus Group. CONSORT 2010 Statement: extension to randomised pilot and feasibility trials. Pilot Feasibility Stud. 2016;2:64.CrossRef Eldridge SM, Chan CL, Campbell MJ, Bond CM, Hopewell S, Thabane L, Lancaster GA, PAFS Consensus Group. CONSORT 2010 Statement: extension to randomised pilot and feasibility trials. Pilot Feasibility Stud. 2016;2:64.CrossRef
8.
go back to reference Morgan B, Hejdenberg J, Hinrichs-Krapels S, Armstrong D. Do feasibility trials contribute to, or avoid, waste in research. PLoS One. 2018;13(4):e0195951.CrossRef Morgan B, Hejdenberg J, Hinrichs-Krapels S, Armstrong D. Do feasibility trials contribute to, or avoid, waste in research. PLoS One. 2018;13(4):e0195951.CrossRef
Metadata
Title
A review of current practice in the design and assessment of internal pilots in UK NIHR clinical trials
Authors
Anna Rosala-Hallas
Carrol Gamble
Jane Blazeby
Paula R. Williamson
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Trials / Issue 1/2019
Electronic ISSN: 1745-6215
DOI
https://doi.org/10.1186/s13063-019-3669-9

Other articles of this Issue 1/2019

Trials 1/2019 Go to the issue