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Participant recruitment into a randomised controlled trial of exercise therapy for people with multiple sclerosis

Overview of attention for article published in Trials, October 2015
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Title
Participant recruitment into a randomised controlled trial of exercise therapy for people with multiple sclerosis
Published in
Trials, October 2015
DOI 10.1186/s13063-015-0996-3
Pubmed ID
Authors

Anouska Carter, Liam Humphreys, Nicky Snowdon, Basil Sharrack, Amanda Daley, Jane Petty, Nicola Woodroofe, John Saxton

Abstract

The success of a clinical trial is often dependant on whether recruitment targets can be met in the required time frame. Despite an increase in research into the benefits of exercise in people with multiple sclerosis (PwMS), no trial has reported detailed data on effective recruitment strategies for large-scale randomised controlled trials. The main purpose of this report is to provide a detailed outline of recruitment strategies, rates and estimated costs in the Exercise Intervention for Multiple Sclerosis (ExIMS) trial to identify best practices for future trials involving multiple sclerosis (MS) patient recruitment. The ExIMS researchers recruited 120 PwMS to participate in a 12-week exercise intervention. Participants were randomly allocated to either exercise or usual-care control groups. Participants were sedentary, aged 18-65 years and had Expanded Disability Status Scale scores of 1.0-6.5. Recruitment strategies included attendance at MS outpatient clinics, consultant mail-out and trial awareness-raising activities. A total of 120 participants were recruited over the course of 34 months. To achieve this target, 369 potentially eligible and interested participants were identified. A total of 60 % of participants were recruited via MS clinics, 29.2 % from consultant mail-outs and 10.8 % through trial awareness. The randomisation yields were 33.2 %, 31.0 % and 68.4 % for MS clinic, consultant mail-outs and trial awareness strategies, respectively. The main reason for ineligibility was being too active (69.2 %), whilst for eligible participants the most common reason for non-participation was the need to travel to the study site (15.8 %). Recruitment via consultant mail-out was the most cost-effective strategy, with MS clinics being the most time-consuming and most costly. To reach recruitment targets in a timely fashion, a variety of methods were employed. Although consultant mail-outs were the most cost-effective recruitment strategy, use of this method alone would not have allowed us to obtain the predetermined number of participants in the required time period, thus leading to costly extensions of the project or failure to reach the number of participants required for sufficient statistical power. Thus, a multifaceted approach to recruitment is recommended for future trials. International Standard Randomised Controlled Trial Registry number: ISRCTN41541516 ; date registered: 5 February 2009.

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The data shown below were compiled from readership statistics for 188 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Spain 1 <1%
Netherlands 1 <1%
Romania 1 <1%
Unknown 185 98%

Demographic breakdown

Readers by professional status Count As %
Student > Master 26 14%
Student > Bachelor 22 12%
Researcher 21 11%
Student > Ph. D. Student 18 10%
Student > Postgraduate 12 6%
Other 43 23%
Unknown 46 24%
Readers by discipline Count As %
Medicine and Dentistry 44 23%
Nursing and Health Professions 31 16%
Sports and Recreations 16 9%
Psychology 11 6%
Neuroscience 6 3%
Other 27 14%
Unknown 53 28%