About this trial
This will be a randomized interventional study. Patients scheduled to undergo a HoLEP at UCSF will be randomized into two groups after the procedure: one group will watch a scripted educational HoLEP video and the other group will not receive a video. We will monitor the post-operative care utilization after discharge. Secondary outcomes will include patient satisfaction.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults aged 18+
Patients scheduled for a HoLEP procedure
Patients willing to complete both baseline and follow up surveys
Patients able to provide informed consent
Disqualifiers
Patients under 18+
Patients unable to consent
Patients unable to complete surveys
Patients without a prostate.
Trial design
Parallel
Treatments tested in this trial
Video
Other interventionParticipants will watch video.
Treatment groups
Trial outcomes
Primary outcomes
Number of Post-operative Healthcare Utilization Events
Healthcare utilization will include MyChart messages, phone calls to clinic, unscheduled clinic visits, hospital readmissions, and emergency/urgent care visits.
Participant Satisfaction Score
Measured using Likert scale survey ranging from 1 (strongly agree) to 5 (strongly disagree).
Sponsors and contacts
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University of California, San Francisco
Lead sponsor
State University of New York - Upstate Medical University
Collaborator
University of Rochester
Collaborator