Projects per year
Patient reported outcomes (PROs) are increasingly assessed in clinical trials, and guidelines are available to inform the design and reporting of such trials. However, researchers involved in PRO data collection report that specific guidance on 'in-trial' activity (recruitment, data collection and data inputting) and the management of 'concerning' PRO data (i.e., data which raises concern for the well-being of the trial participant) appears to be lacking. The purpose of this review was to determine the extent and nature of published guidelines addressing these areas.
FingerprintDive into the research topics of 'Patient reported outcomes (PROs) in clinical trials : is 'in-trial' guidance lacking? a systematic review'. Together they form a unique fingerprint.
- 1 Finished
Linked to a/c DMAB.RRAK14731 Midland Hub for Trials Methodology Research at University of Birmingham
1/06/09 → 31/05/14
Project: Research Councils