Abstract
BackgroundRecruitment to randomised controlled trials (RCTs) can be challenging, with most trials not reaching recruitment targets. Randomised feasibility studies can be set up prior to a main trial to identify and overcome recruitment obstacles. This paper reports on an intervention—the QuinteT Recruitment Intervention (QRI)—to optimise recruitment within a randomised feasibility study of surgical treatments for patients with Dupuytren’s contracture (the HAND-1 study).MethodsThe QRI was introduced in 2-phases: phase 1 sought to understand the recruitment challenges by interviewing trial staff, scrutinising screening logs and analysing audio-recorded patient consultations; in phase 2 a tailored plan of action consisting of recruiter feedback and training was delivered to address the identified challenges.ResultsTwo key recruitment obstacles emerged: (1) issues with the recruitment pathway, in particular methods to identify potentially eligible patients and (2) equipoise of recruiters and patients. These were addressed by liaising with centres to share good practice and refine their pathway and by providing bespoke feedback and training on consent discussions to individual recruiters and centres whilst recruitment was ongoing. The HAND-1 study subsequently achieved its recruitment target.ConclusionsTransferable lessons learnt from the QRI in the feasibility study will be implemented in the definitive RCT, enabling a “head start” in the tackling of wider issues around screening methods and consent discussions in the set up/early recruitment study phases, with ongoing QRI addressing specific issues with new centres and recruiters. Findings from this study are likely to be relevant to other surgical and similar trials that are anticipated to encounter issues around patient and recruiter equipoise of treatments and variation in recruitment pathways across centres. The study also highlights the value of feasibility studies in fine-tuning design and conduct issues for definitive RCTs. Embedding a QRI in an RCT, at feasibility or main stage, offers an opportunity for a detailed and nuanced understanding of key recruitment challenges and the chance to address them in “real-time” as recruitment proceeds.
Highlights
Recruitment to randomised controlled trials (RCTs) can be challenging, with most trials not reaching recruitment targets
This paper reports on an intervention embedded into a feasibility hand surgery RCT that aimed to identify and overcome barriers to recruitment and informed consent prior to a main trial
Seventy-one (46%) of these were randomised to receive needle fasciotomy (NF) or limited fasciectomy (LF), which was within the pre-set recruitment target range of 50–85 participants demonstrating that a main trial would be feasible
Summary
Recruitment to randomised controlled trials (RCTs) can be challenging, with most trials not reaching recruitment targets. This paper reports on an intervention—the QuinteT Recruitment Intervention (QRI)—to optimise recruitment within a randomised feasibility study of surgical treatments for patients with Dupuytren’s contracture (the HAND-1 study). This paper reports on an intervention embedded into a feasibility hand surgery RCT that aimed to identify and overcome barriers to recruitment and informed consent prior to a main trial. There is a lack of high-quality evidence comparing two surgical treatments for primary Dupuytren’s contracture: limited fasciectomy (LF) and needle fasciotomy (NF) [6]. Both NF and LF are currently performed within the National Health Service (NHS) in England. Dupuytren’s contracture can come back after both NF and LF, such that further surgery may be needed, though recurrence is more common after NF [7]
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