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Clinical Trials/NCT07644819
NCT07644819Not yet recruitingNot Applicable

Reducing No-Shows in High-Risk Urology Patients Through Enhanced Preoperative Outreach

University of California, San Francisco1 site in 1 country68 target enrollmentStarted: August 1, 2026Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
68
Locations
1
Primary Endpoint
Procedure No-Show Rate

Study Overview

Brief 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Adults aged 18 years or older
  • •Identified as high risk for no-show by the study predictive model
  • •Scheduled to undergo a urologic procedure at UCSF/UCSF affiliated sites

Exclusion Criteria

  • •Younger than 18 years of age
  • •Not scheduled for a urologic procedure

Arms & Interventions

Standard Care

No Intervention

Participants receive standard preoperative care, including procedure scheduling, preoperative anesthesia evaluation, and routine surgery center reminder calls.

Enhanced Preoperative Outreach

Experimental

Participants receive standard care plus reminder phone calls at 7 days, 3 days, 1 day, and the day of the procedure, text messaging access, assessment of barriers to attendance, and referral to social work when appropriate.

Intervention: Preoperative Outreach (Behavioral)

Outcomes

Primary Outcomes

Procedure No-Show Rate

Time Frame: From enrollment until the scheduled procedure date (up to 8 weeks)

Whether the participant attended their scheduled urologic procedure

Secondary Outcomes

  • Procedure Rescheduling Rate(From enrollment until the scheduled procedure date (up to 8 weeks))

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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