A comparison of socio-demographic and psychological factors between patients consenting to randomisation and those selecting treatment (the ProtecT study)

Mills, Nicola; Metcalfe, Chris; Ronsmans, Carine; Davis, Michael; Lane, J. Athene; Sterne, Jonathan A.C.; Peters, Tim J.; Hamdy, Freddie C.; Neal, David E.; Donovan, Jenny L.

doi:10.1016/j.cct.2006.04.008

« Previous Next »Contemporary Clinical Trials
Volume 27, Issue 5 , Pages 413-419, October 2006

A comparison of socio-demographic and psychological factors between patients consenting to randomisation and those selecting treatment (the ProtecT study)

Nicola Mills
- Department of Social Medicine, University of Bristol, U.K.
- Corresponding author. Department of Social Medicine, University of Bristol, Canynge Hall, Whiteladies Road, Bristol, BS8 2PR, U.K. Tel.: +44 117 9287210; fax: +44 117 9287292.
Chris Metcalfe
- Department of Social Medicine, University of Bristol, U.K.
Carine Ronsmans
- London School of Hygiene and Tropical Medicine, University of London, U.K.
Michael Davis
- Department of Social Medicine, University of Bristol, U.K.
J. Athene Lane
- Department of Social Medicine, University of Bristol, U.K.
Jonathan A.C. Sterne
- Department of Social Medicine, University of Bristol, U.K.
Tim J. Peters
- Academic Unit of Primary Health Care, Department of Community Based Medicine, University of Bristol, U.K.
Freddie C. Hamdy
- Division of Clinical Sciences, University of Sheffield, U.K.
David E. Neal
- Uro-oncology, Cancer Centre, University of Cambridge, U.K.
Jenny L. Donovan
- Department of Social Medicine, University of Bristol, U.K.

Received 15 June 2005; accepted 12 April 2006.

Abstract

Background

Patient preferences for treatment can pose problems for the conduct of randomised controlled trials: patients with a preference may refuse participation and thereby potentially compromise external validity. Moreover, randomising patients with a preference may affect treatment efficacy and threaten internal validity.

Aims

This study compared baseline characteristics and short-term psychological outcomes of patients who selected their treatment and those who agreed to random allocation.

Methods

Men participating in the prostate testing for cancer and treatment (ProtecT) study and who were randomised to active monitoring (n=138) were compared with those who had refused randomisation and selected this management (n=180). Socio-demographic data were collected at baseline, and anxiety and depression data were collected at baseline and six month follow-up. Socio-demographic characteristics were compared across these two groups in univariable analyses, and then linear regression was used to compare levels of anxiety and depression at follow-up with adjustments for confounders.

Results

Participants who selected active monitoring were more affluent (based on occupation details) and had less anxiety at baseline than those who were randomised. There were no differences with respect to age and marital status. Levels of anxiety and depression at six months follow-up were similar across the two groups of men.

Conclusions

This study found some differences at baseline between the socio-demographic and psychological status of those randomised and self-selecting treatment, but no psychological differences at short-term follow-up. Further empirical evidence is required to assess whether preferences impact upon the process and outcome of randomised controlled trials.

Keywords: Randomised controlled trial, Trial participation, Patient treatment preferences, Prostate cancer