Trials and tribulations of recruiting 2,000 older women onto a clinical trial investigating falls and fractures : vital D study

Sanders, Kerrie M., Stuart, Amanda L., Merriman, Elizabeth N., Read, Meaghan L., Kotowicz, Mark A., Young, Doris, Taylor, Roderick, Blair-Holt, Ian, Mander, Alistair G. and Nicholson, Geoffrey C. 2009, Trials and tribulations of recruiting 2,000 older women onto a clinical trial investigating falls and fractures : vital D study, BMC medical research methodology, vol. 9, no. 78.

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Title Trials and tribulations of recruiting 2,000 older women onto a clinical trial investigating falls and fractures : vital D study
Author(s) Sanders, Kerrie M.
Stuart, Amanda L.
Merriman, Elizabeth N.
Read, Meaghan L.
Kotowicz, Mark A.
Young, Doris
Taylor, Roderick
Blair-Holt, Ian
Mander, Alistair G.
Nicholson, Geoffrey C.
Journal name BMC medical research methodology
Volume number 9
Issue number 78
Total pages 10
Publisher BioMed Central
Place of publication London, England
Publication date 2009
ISSN 1471-2288
Summary Background Randomised, placebo-controlled trials are needed to provide evidence demonstrating safe, effective interventions that reduce falls and fractures in the elderly. The quality of a clinical trial is dependent on successful recruitment of the target participant group. This paper documents the successes and failures of recruiting over 2,000 women aged at least 70 years and at higher risk of falls or fractures onto a placebo-controlled trial of six years duration. The characteristics of study participants at baseline are also described for this study.

Methods The Vital D Study recruited older women identified at high risk of fracture through the use of an eligibility algorithm, adapted from identified risk factors for hip fracture. Participants were randomised to orally receive either 500,000 IU vitamin D3 (cholecalciferol) or placebo every autumn for five consecutive years. A variety of recruitment strategies were employed to attract potential participants.

Results Of the 2,317 participants randomised onto the study, 74% (n = 1716/2317) were consented onto the study in the last five months of recruiting. This was largely due to the success of a targeted mail-out. Prior to this only 541 women were consented in the 18 months of recruiting. A total of 70% of all participants were recruited as a result of targeted mail-out. The response rate from the letters increased from 2 to 7% following revision of the material by a public relations company. Participant demographic or risk factor profile did not differ between those recruited by targeted mail-outs compared with other methods.

Conclusion The most successful recruitment strategy was the targeted mail-out and the response rate was no higher in the local region where the study had extensive exposure through other recruiting strategies. The strategies that were labour-intensive and did not result in successful recruitment include the activities directed towards the GP medical centres. Comprehensive recruitment programs employ overlapping strategies simultaneously with ongoing assessment of recruitment rates. In our experience, and others direct mail-outs work best although rights to privacy must be respected.
Language eng
Field of Research 119999 Medical and Health Sciences not elsewhere classified
Socio Economic Objective 970111 Expanding Knowledge in the Medical and Health Sciences
HERDC Research category C1.1 Refereed article in a scholarly journal
Copyright notice ©2009, Sanders et al.
Persistent URL http://hdl.handle.net/10536/DRO/DU:30047627

Document type: Journal Article
Collection: School of Medicine
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