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Successful and unsuccessful recruitment and retainment strategies in a UK multicentre drug trial for a rare chronic pain condition which performed above target
Author(s) -
Jatinder Bisla,
Gareth Ambler,
Bernhard Frank,
Sumit Gulati,
Poppy Hocken,
Mairi James,
Joanna Kelly,
Jocelyn Keshet-Price,
Candy McCabe,
Deborah McGylnn,
Nick Padfield,
David Pang,
Gill Pout,
Mark Sanders,
Mick Serpell,
Nicholas Shenker,
Karim Shoukrey,
Samuel Wesley,
Margaret Weston,
Beverly White-Alao,
Lynne Wyatt,
Caroline Murphy,
Andreas Göebel
Publication year - 2019
Publication title -
british journal of pain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.642
H-Index - 15
eISSN - 2049-4645
pISSN - 2049-4637
DOI - 10.1177/2049463719893399
Subject(s) - medicine , clinical trial , audit , chronic pain , patient recruitment , physical therapy , population , alternative medicine , intensive care medicine , pathology , management , environmental health , economics
Recruitment into trials in rare chronic pain conditions can be challenging, so such trials consequently are underpowered or fail.Methods: Drawing from our experience in conducting, to date, the largest academic trial in a rare chronic pain condition, complex regional pain syndrome, we have identified recruitment and retention strategies for successful trial conduct.Results: We present 13 strategies grouped across the categories of ‘setting the recruitment rate’, ‘networking’, ‘patient information’, ‘trial management’ and ‘patient retention’. Moreover, six recruitment risks are also discussed. A conservative recruitment estimate, based on audits of newly referred patients to the trial centres without taking into account availability of ‘old’ patients or recruitment from outside centres, and assuming a 55% patient refusal rate yielded accurate numbers.Conclusion: Appreciation of these identified recruitment challenges and opportunities may contribute to supporting prospective investigators when they design clinical trials for chronic pain patient population groups where it has been historically difficult to conduct high-quality and robust clinical trials.

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