ORCID
- Carroll, Camille: 0000-0001-7472-953X
Abstract
Promotion of research is a key strategy of the National Health Service (NHS). Currently, many patients are not afforded the opportunity to participate in clinical studies. A register of research-interested patients has the potential to maximise inclusivity. We have established a register of research-interested patients with Parkinson's disease within the South West of England, with pragmatic inclusion criteria and multiple recruitment routes. We undertook an analysis of the register, investigation of its utility as a recruitment tool and a survey of recruiters. There were 529 active participants; 30% were self-referred and 70% were recruited by a healthcare practitioner. Response rate to annual questionnaires was 86.5%. Staff time required for pack preparation, recruitment and data entry was 15 min per new recruit and 5 min per follow-up questionnaire. In total, 85% of recruiters viewed the register positively. A single mailing to participants resulted in a recruitment rate that significantly exceeded that achieved by traditional recruitment methods.
DOI
10.7861/clinmedicine.12-3-210
Publication Date
2012-06-01
Publication Title
Clin Med (Lond)
Volume
12
Issue
3
First Page
210
Last Page
215
ISSN
1470-2118
Organisational Unit
Peninsula Medical School
Keywords
Aged, Biomedical Research, Clinical Trials as Topic, Female, Humans, Male, Parkinson Disease, Patient Participation, Patient Selection, Program Development, Registries, United Kingdom
Recommended Citation
Carroll, C., Palmer, A., Cosby, C., & Zajicek, J. (2012) 'Analysis and validation of a Parkinson's disease register as a recruitment tool for clinical studies.', Clin Med (Lond), 12(3), pp. 210-215. Available at: https://doi.org/10.7861/clinmedicine.12-3-210
