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Educational Discharge Video Impact on Post-Operative Healthcare Utilization After HoLEP

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.

Condition(s)HoLEP, Patient Satisfaction, Educational Video Intervention
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryThis 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.
Who can participateInclusion Criteria: 1. Adults aged 18+ 2. Patients scheduled for a HoLEP procedure 3. Patients willing to complete both baseline and follow up surveys 4. Patients able to provide informed consent 5. Patients are English-speaking and understand English Exclusion Criteria: 1. Patients under 18+ 2. Patients unable to consent 3. Patients unable to complete surveys 4. Patients without a prostate. 5. Patients are non-English speakers
Ages18 Years
SexMale
Lead sponsorUniversity of California, San Francisco
LocationsSan Francisco, California, United States; Rochester, New York, United States; Syracuse, New York, United States
Start date2025-11-04
NCT IDNCT06975033
Official listinghttps://clinicaltrials.gov/study/NCT06975033

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