video
OtherParticipants will watch video.
NCT Number: NCT06975033
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.
Interested in participating?
Request Info18 year and older
Male
Interventional
Not applicable
University of California, San Francisco, San Francisco, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will watch video.
Time frame: 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.
Time frame: 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).
Contact information is provided by the study sponsor or research team.
University of California, San Francisco
Other
The Impact of Discharge Educational Discharge Videos on Post-Operative Care Utilization After Holmium Laser Enucleation of the Prostate (HoLEP) Procedures
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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