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NCT07692789From ClinicalTrials.govRecruiting

Improving Uroflowmetry Interpretability: Evaluating the Impact of Patient Reminder Systems

  • Pelvic Organ Prolapse
  • Urinary Incontinence

At a glance

Phase
Phase not stated
Study type
Interventional
Sponsor
Ohio State University
Enrolment target
162
Started
November 2026
Main results due
June 2027
Study sites
1
Registry updated
24 September 2026

Can you take part?

  • Aged 18 years and over.
  • Women only.
  • You need the condition being studied — healthy volunteers are not accepted.

These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.

Read the full 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.

What this study is about

In the sponsor’s own words, from the registry.

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.

Study sites(1)

  • Ohio State University Wexner Medical Center

    Columbus, Ohio, United States

    Recruiting

Showing 1 of 1 sites. 1 of the 1 site on this study is recruiting right now — a site can stop enrolling while the study as a whole is still open.

Source: ClinicalTrials.gov record NCT07692789. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.

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Improving Uroflowmetry Interpretability: Evaluating the Impact of Patient Reminder Systems | Trialion