114 Participants Needed

Educational Video for Health Education After Prostate Procedure

Recruiting at 2 trial locations
DB
Overseen ByDavid Bayne, MD, MPH
Age: 18+
Sex: Male
Trial Phase: Academic
Sponsor: University of California, San Francisco
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

Trial Summary

What is the purpose of this trial?

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.

Research Team

DB

David Bayne, MD, MPH

Principal Investigator

University of California, San Francisco

Eligibility Criteria

This trial is for patients scheduled to undergo a HoLEP procedure at UCSF. There are no specific inclusion or exclusion criteria provided, so it's open to those who are part of the patient population undergoing this surgery and willing to participate in the study.

Inclusion Criteria

Patients are English-speaking and understand English
Patients able to provide informed consent
I am scheduled for a HoLEP procedure.
See 1 more

Exclusion Criteria

Patients are non-English speakers
Patients unable to complete surveys
I do not have a prostate.
See 1 more

Timeline

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Procedure

Participants undergo the Holmium Laser Enucleation of the Prostate (HoLEP) procedure

1 day

Post-operative Monitoring

Participants are monitored for post-operative care utilization and patient satisfaction

8 weeks
Follow-up visits as needed

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

Treatment Details

Interventions

  • Video
Trial Overview The study is testing whether watching an educational video after HoLEP surgery affects how much post-operative care patients use. It also looks at patient satisfaction. Participants will be randomly placed into two groups; one watches the video, while the other does not.
Participant Groups
2Treatment groups
Experimental Treatment
Active Control
Group I: VideoExperimental Treatment1 Intervention
Participants will watch video.
Group II: No VideoActive Control1 Intervention
Participants will not watch video.

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of California, San Francisco

Lead Sponsor

Trials
2,636
Recruited
19,080,000+

State University of New York - Upstate Medical University

Collaborator

Trials
176
Recruited
27,600+

University of Rochester

Collaborator

Trials
883
Recruited
555,000+
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