Improving Uroflowmetry Interpretability: Evaluating the Impact of Patient Reminder Systems

Recruiting now · Not applicable

Conditions studied: Pelvic Organ Prolapse, Urinary Incontinence

In brief

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.

Key facts

Study ID

NCT07692789

Run by

Ohio State University

People needed

162

Starts

2026-07-01

Expected to finish

2027-12-01

Last updated by the study team

2026-07-31

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Age 18 years or older
• Sex assigned at birth: Female.
• English-speaking
• Scheduled to undergo a urodynamics study at the OSU Upper Arlington Outpatient Clinic, OSU New Albany Outpatient Clinic, or OSU Eye and Ear Institute
• Ability to access a telephone
• Active MyChart account
• Ability to provide informed consent
• Documented post-residual volume of less than 150 mL
• Ability to be reached by telephone after three call attempts
• Negative point-of-care urinary tract infection on the day of the scheduled procedure (SOC)

You may not qualify if…

• Under 18 years of age
• 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.
• Men are excluded as the population of interest is the female urogynecology population in both urology and obstetrics and gynecology.
• 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.
• Individuals who cannot be reached by telephone are excluded because they cannot receive the intervention.
• 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.

Where it is running

• Ohio State University Wexner Medical Center — Columbus, Ohio, United States (enrolling)

Full record on ClinicalTrials.gov

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