Status
Conditions
Treatments
About
This study will assess, by means of a randomized controlled trial, the impact of an online educational tool, on doctors' knowledge and confidence with regards to prescribing for older patients.
Full description
Both control and intervention groups will complete assessments at baseline, 4 weeks post intervention and 8 weeks post intervention.
Differences in mean test scores will be the primary outcome measure.
Qualitative information exploring doctors' attitudes and confidence, pre and post intervention will also be collected and will be a secondary outcome
Enrollment
Sex
Volunteers
Inclusion criteria
Exclusion criteria
100 participants in 2 patient groups
Loading...
Central trial contact
Stephen Byrne, MPharm, PhD; Shane Cullinan, BPharm
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal