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A framework for prospectively defining progression rules for internal pilot studies monitoring recruitment
Lisa V Hampson1,2, Paula R Williamson3, Martin J Wilby4
11 Department of Mathematics and Statistics, Medical and Pharmaceutical Statistics Research Unit, Lancaster University, Lancaster, UK.
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.
Insights
Many clinical trials fail to meet recruitment targets, risking underpowered results. This study introduces a framework for internal pilot studies with pre-specified progression rules to optimize trial planning and resource allocation.
Area of Science:
- Clinical Trial Design
- Biostatistics
- Health Services Research
Background:
- Publicly funded trials frequently miss recruitment targets within planned durations.
- Missed recruitment can lead to decisions about extending funding or facing underpowered analyses.
- Current feasibility assessments and progression rules are often ad hoc and lack criteria for evaluating recruitment strategy adaptations.
Purpose of the Study:
- To develop a framework for planning and designing internal pilot studies.
- To enable early trial termination for poor recruitment or continuation for adequate enrolment.
- To establish pre-specified, optimal progression rules for internal pilot studies.
Main Methods:
- Development of a novel two-stage design for internal pilot studies.
- Derivation of optimal progression rules to minimize expected trial overrun.
- Incorporation of criteria for evaluating the success of recruitment strategy adaptations.
Main Results:
- The proposed framework allows for pre-specified progression rules agreed upon before trial commencement.
- It provides a method to stop trials early if recruitment is insufficient or continue if adequate.
- The framework includes evaluating recruitment adaptations when initial progress is neither sufficient nor insufficient.
Conclusions:
- The developed framework offers a structured approach to internal pilot studies, improving trial planning and efficiency.
- Optimal progression rules minimize delays and maximize the probability of successful study completion.
- This methodology addresses the need for robust, pre-specified criteria in clinical trial recruitment and adaptation.
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