About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
Younger than 18 years of age
Not scheduled for a urologic procedure
Trial design
Treatments tested in this trial
- Preoperative Outreach