Educational Discharge Video Impact on Post-Operative Healthcare Utilization After HoLEP
The Impact of Discharge Educational Discharge Videos on Post-Operative Care Utilization After Holmium Laser Enucleation of the Prostate (HoLEP) Procedures
1 other identifier
interventional
114
1 country
3
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2025
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 4, 2025
CompletedFirst Posted
Study publicly available on registry
May 16, 2025
CompletedStudy Start
First participant enrolled
November 4, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
April 16, 2026
April 1, 2026
1.1 years
April 4, 2025
April 13, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
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.
up to 90 days (estimated time frame between initial surgery and first follow up visit)
Participant Satisfaction Score
Measured using Likert scale survey ranging from 1 (strongly agree) to 5 (strongly disagree).
up to 90 days (estimated time frame between initial surgery and first follow up visit)
Study Arms (2)
Video
EXPERIMENTALParticipants will watch video.
No Video
NO INTERVENTIONParticipants will not watch video.
Interventions
Eligibility Criteria
You may qualify if:
- 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
- Patients are English-speaking and understand English
You may not qualify if:
- Patients under 18+
- Patients unable to consent
- Patients unable to complete surveys
- Patients without a prostate.
- Patients are non-English speakers
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (3)
University of California, San Francisco
San Francisco, California, 94143, United States
University of Rochester Medical Center
Rochester, New York, 14620, United States
Scott SUNY Upstate Medical University
Syracuse, New York, 13210, United States
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
David Bayne, MD, MPH
University of California, San Francisco
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 4, 2025
First Posted
May 16, 2025
Study Start
November 4, 2025
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
April 16, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share