Educational Video Intervention, HoLEP, Patient Satisfaction
Conditions
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.
Interventions
OTHERVideo
Participants will watch video.
Sponsors
University of California, San Francisco
State University of New York - Upstate Medical University
University of Rochester
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion 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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Post-operative Healthcare Utilization Events | up to 90 days (estimated time frame between initial surgery and first follow up visit) | Healthcare utilization will include MyChart messages, phone calls to clinic, unscheduled clinic visits, hospital readmissions, and emergency/urgent care visits. |
| Participant Satisfaction Score | up to 90 days (estimated time frame between initial surgery and first follow up visit) | Measured using Likert scale survey ranging from 1 (strongly agree) to 5 (strongly disagree). |
Countries
United States
Contacts
CONTACTDavid Bayne, MD, MPH
PRINCIPAL_INVESTIGATORDavid Bayne, MD, MPH
University of California, San Francisco
Outcome results
None listed