Educational Discharge Video Impact on Post-Operative Healthcare Utilization After HoLEP
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18+
SponsorUniversity of California, San Francisco
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
Qualifiers
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
Treatments tested in this trial
- Video
Treatment groups
114 Participants
are divided into 2 treatment groupsSponsors and collaborators
University of California, San Francisco
Lead sponsor
State University of New York - Upstate Medical University
Collaborator
University of Rochester
Collaborator
Source ClinicalTrials.gov