Clinical Trial

Preoperative Outreach to Improve Surgical Attendance

Not Yet Recruiting
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Summary
This study aims to evaluate the impact of reminder call intervention on no-shows for urologic procedures in patients identified to be high risk for no-showing. Patients scheduled to undergo a urologic procedure will be randomized into two groups: the intervention group, who receives a series of reminder calls and text messages about appointment details and patient questions prior to the procedure date; and the control group, who receives standard care only. Secondary outcomes include rates of patient re-scheduling and healthcare utilization.
Trial Details
NCT Number NCT07644819
Lead Sponsor University of California, San Francisco
Conditions Urology
Enrollment 68 participants
Start Date 2026-08
Primary Completion 2026-12 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2026-08-13