Literature DB >> 28589752

A framework for prospectively defining progression rules for internal pilot studies monitoring recruitment.

Lisa V Hampson1,2, Paula R Williamson3, Martin J Wilby4, Thomas Jaki1.   

Abstract

Just over half of publicly funded trials recruit their target sample size within the planned study duration. When recruitment targets are missed, the funder of a trial is faced with the decision of either committing further resources to the study or risk that a worthwhile treatment effect may be missed by an underpowered final analysis. To avoid this challenging situation, when there is insufficient prior evidence to support predicted recruitment rates, funders now require feasibility assessments to be performed in the early stages of trials. Progression criteria are usually specified and agreed with the funder ahead of time. To date, however, the progression rules used are typically ad hoc. In addition, rules routinely permit adaptations to recruitment strategies but do not stipulate criteria for evaluating their effectiveness. In this paper, we develop a framework for planning and designing internal pilot studies which permit a trial to be stopped early if recruitment is disappointing or to continue to full recruitment if enrolment during the feasibility phase is adequate. This framework enables a progression rule to be pre-specified and agreed upon prior to starting a trial. The novel two-stage designs stipulate that if neither of these situations arises, adaptations to recruitment should be made and subsequently evaluated to establish whether they have been successful. We derive optimal progression rules for internal pilot studies which minimise the expected trial overrun and maintain a high probability of completing the study when the recruitment rate is adequate. The advantages of this procedure are illustrated using a real trial example.

Keywords:  Internal pilot; operational feasibility; operational power; progression rule; randomised controlled trial; recruitment

Mesh:

Substances:

Year:  2017        PMID: 28589752     DOI: 10.1177/0962280217708906

Source DB:  PubMed          Journal:  Stat Methods Med Res        ISSN: 0962-2802            Impact factor:   3.021


  6 in total

1.  Youth Culturally adapted Manual Assisted Problem Solving Training (YCMAP) in Pakistani adolescent with a history of self-harm: protocol for multicentre clinical and cost-effectiveness randomised controlled trial.

Authors:  Nusrat Husain; Sehrish Tofique; Imran B Chaudhry; Tayyeba Kiran; Peter Taylor; Christopher Williams; Rakhshi Memon; Shilpa Aggarwal; Mohsin Hassan Alvi; S Ananiadou; Moin Ahmad Ansari; Saadia Aseem; Andrew Beck; Sumira Alam; Erminia Colucci; Kate Davidson; Sarah Edwards; Richard Emsley; Jonathan Green; Anil Gumber; Keith Hawton; Farhat Jafri; Ayesha Khaliq; Thomas Mason; Ann Mcreath; Ayesha Minhas; Farooq Naeem; Haider Ali Naqvi; Amna Noureen; Maria Panagioti; Anita Patel; Aaron Poppleton; Tinevimbo Shiri; Mima Simic; Sarwat Sultan; Asad Tamizuddin Nizami; Zainab Zadeh; Shehla Naeem Zafar; Nasim Chaudhry
Journal:  BMJ Open       Date:  2022-05-13       Impact factor: 3.006

2.  Guidance for using pilot studies to inform the design of intervention trials with continuous outcomes.

Authors:  Melanie L Bell; Amy L Whitehead; Steven A Julious
Journal:  Clin Epidemiol       Date:  2018-01-18       Impact factor: 4.790

Review 3.  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
Journal:  Trials       Date:  2019-09-18       Impact factor: 2.279

4.  The reporting of progression criteria in protocols of pilot trials designed to assess the feasibility of main trials is insufficient: a meta-epidemiological study.

Authors:  Lawrence Mbuagbaw; Sarah Daisy Kosa; Daeria O Lawson; Rosa Stalteri; Oluwatobi R Olaiya; Ahlam Alotaibi; Lehana Thabane
Journal:  Pilot Feasibility Stud       Date:  2019-11-03

5.  Applying mixed methods to pilot feasibility studies to inform intervention trials.

Authors:  Kelly A Aschbrenner; Gina Kruse; Joseph J Gallo; Vicki L Plano Clark
Journal:  Pilot Feasibility Stud       Date:  2022-09-26

6.  Adding flexibility to clinical trial designs: an example-based guide to the practical use of adaptive designs.

Authors:  Thomas Burnett; Pavel Mozgunov; Philip Pallmann; Sofia S Villar; Graham M Wheeler; Thomas Jaki
Journal:  BMC Med       Date:  2020-11-19       Impact factor: 8.775

  6 in total

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