Educational Discharge Video Impact on Post-Operative Healthcare Utilization After HoLEP
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Video.
- Who it may be relevant to
- Registry conditions: HoLEP, Patient Satisfaction, Educational Video Intervention. Basic parameters: from 18 years · Male.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
The Impact of Discharge Educational Discharge Videos on Post-Operative Care Utilization After Holmium Laser Enucleation of the Prostate (HoLEP) Procedures
Overview
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.
Interventions
- Other Video
Participants will watch video.
Primary outcome measures
- Number of Post-operative Healthcare Utilization Events [Time frame: up to 90 days (estimated time frame between initial surgery and first follow up visit)]
- Participant Satisfaction Score [Time frame: up to 90 days (estimated time frame between initial surgery and first follow up visit)]
Eligibility criteria
Inclusion criteria
- 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
Exclusion criteria
- Patients under 18+
- Patients unable to consent
- Patients unable to complete surveys
- Patients without a prostate.
- Patients are non-English speakers
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Other
Study locations
United States · 3 centers
- University of California, San Francisco — San Francisco
- University of Rochester Medical Center — Rochester
- Scott SUNY Upstate Medical University — Syracuse
Identifiers
NCT: NCT06975033 · 25-43311