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NCT07692789
Improving Uroflowmetry Interpretability: Evaluating the Impact of Patient Reminder Systems
Conditions: Pelvic Organ Prolapse, Urinary Incontinence
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 162
Sponsor: Ohio State University
Location: Ohio State University Wexner Medical Center Columbus Ohio
Summary
The purpose of this study is to evaluate the impact of pre-procedure patient reminder systems on patient satisfaction, preparedness, and anxiety among patients undergoing urodynamics studies. The rate of successful procedure completion will be compared between a prospective intervention group and a historical control group to determine whether the intervention improves procedural success and healthcare delivery.
Eligibility Criteria
Inclusion Criteria
1. Age 18 years or older
2. Sex assigned at birth: Female.
3. English-speaking
4. Scheduled to undergo a urodynamics study at the OSU Upper Arlington Outpatient Clinic, OSU New Albany Outpatient Clinic, or OSU Eye and Ear Institute
5. Ability to access a telephone
6. Active MyChart account
7. Ability to provide informed consent
8. Documented post-residual volume of less than 150 mL
9. Ability to be reached by telephone after three call attempts
10. Negative point-of-care urinary tract infection on the day of the scheduled procedure (SOC)
Exclusion criteria:
1. Under 18 years of age
2. Patients with structural causes of urinary retention/incomplete bladder emptying (defined as a post-void residual \>150ml) or a positive point-of-care urinary tract infection on the day of the procedure.
3. Men are excluded as the population of interest is the female urogynecology population in both urology and obstetrics and gynecology.
4. Patients without access to a telephone or an active MyChart account are excluded because the intervention relies on telephone calls and electronic messaging for delivery of pre-procedure education and reminders.
5. Individuals who cannot be reached by telephone are excluded because they cannot receive the intervention.
6. Non-English speaking individuals are excluded because they will not be able to receive the standardized phone call in English and will not be able to complete the informed consent.
Source: ClinicalTrials.gov (NCT07692789). StuddyBuddy aggregates publicly available trial information.