162 Participants NeededMy employer runs this trial

Patient Reminder System for Urinary Incontinence

LH
AS
Overseen ByAshka Shah
Age: 18+
Sex: Female
Trial Phase: Academic
Sponsor: Ohio State University
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to determine if reminders before a urodynamics test can help patients feel more prepared and less anxious. The study will compare two groups: one receiving reminder phone calls and another from past records who did not. Women who speak English, have experienced urinary issues, and are scheduled for a urodynamics test at specific OSU clinics may be suitable candidates, particularly if they can be reached by phone. As an unphased trial, this study allows participants to contribute to enhancing patient care and reducing anxiety during medical procedures.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.

What prior data suggests that this patient reminder system is safe?

Research has shown that reminder systems for patients are generally safe and easy to use. These systems send reminders about upcoming medical appointments or procedures, helping people attend and prepare better. Studies have not identified any negative effects from using these reminder systems. Because the reminder system in this study is similar, it is expected to be safe for participants.12345

Why are researchers excited about this trial?

Researchers are excited about this trial because it explores a patient reminder system for managing urinary incontinence, a condition where patients often forget crucial pre-appointment instructions. This system is unique because it involves personalized phone calls to patients, reminding them to arrive with a comfortably full bladder — an essential step for accurate urodynamics studies. By potentially improving patient compliance and study accuracy, this approach could enhance patient care and streamline clinical workflows, differentiating it from other treatments that primarily focus on medication or physical therapy.

What evidence suggests that the patient reminder system is effective for improving procedural success in urodynamics studies?

This trial will evaluate the effectiveness of a patient reminder system for urinary incontinence. Studies have shown that reminding patients about their treatments can improve healthcare by helping them adhere to their treatment plans, including for urinary incontinence (difficulty controlling urination). Research suggests that these reminders can increase patient satisfaction and preparedness for medical tests, such as urodynamic studies, which identify the causes of urinary problems. One study found that digital reminders improved outcomes, making patients more likely to attend appointments and complete procedures. Although specific data on reminder systems for urinary incontinence is limited, positive effects in other areas suggest these systems could enhance procedure success and the overall patient experience. Participants in this trial will either receive a reminder call before their scheduled urodynamic studies or be part of a historical control group without such reminders.56789

Are You a Good Fit for This Trial?

This trial is for people scheduled to have a urodynamics test due to pelvic organ prolapse or urinary incontinence. Participants should be able to receive reminders before their procedure.

Inclusion Criteria

English-speaking
Documented post-residual volume of 150 mL
Ability to access a telephone
See 7 more

Exclusion Criteria

Patients without access to a telephone or an active MyChart account
I have urinary retention from a physical problem or a current urinary tract infection.
Individuals who cannot be reached by telephone
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1 week

Intervention

Participants receive a phone call reminder before their scheduled urodynamics study

Less than 1 week
1 phone call

Follow-up

Participants are monitored for satisfaction, preparedness, and anxiety after the urodynamics study

Less than 1 week

What Are the Treatments Tested in This Trial?

Interventions

  • Patient reminder system

Trial Overview

The study is testing whether sending patients reminders before their urodynamics test helps more people successfully complete the procedure, and if it affects satisfaction, preparedness, and anxiety compared to those who did not get reminders.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: using patient reminder systems before scheduled urodynamics studiesExperimental Treatment1 Intervention
Group II: not using patient reminder systems before scheduled urodynamics studiesActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Ohio State University

Lead Sponsor

Trials
891
Recruited
2,659,000+

Citations

Study Details | NCT07692789 | Improving Uroflowmetry ...

Evaluate patient satisfaction and preparedness before and after a urodynamic study after delivery of a patient reminder system.

Revi System demonstrates positive two-year results for ...

Key findings include a durable reduction in UUI episodes, with 79% of participants experiencing at least a 50% decrease in symptoms and 56% ...

Identification of preferred reminder systems and patient ...

This study is the first to explore patient preferences for reminder modalities to help promote treatment adherence for UI.

The effectiveness of digital therapeutics for rehabilitation of ...

This review suggests that digital therapeutics-based interventions may be significantly more effective than controls in alleviating urinary ...

A Randomized Trial of Urodynamic Testing before Stress ...

Urodynamic studies are commonly performed in women before surgery for stress urinary incontinence, but there is no good evidence that they improve outcomes.

Devices Indicated for the Treatment of Urinary Incontinence

This guidance document describes FDA's recommendations for clinical investigations of medical devices indicated for the treatment of urinary incontinence.

Identification of preferred reminder systems and patient factors ...

This study is the first to explore patient preferences for reminder modalities to help promote treatment adherence for UI.

OASIS Pivotal Trial Results for Revi System

The trial results demonstrate a statistically significant improvement with a 78.4% clinical success rate as defined by at least a 50% reduction in UUI at 12 ...

Articles App-based therapy for female patients with urinary ...

Outcomes. The primary endpoint was the relative change from baseline of the incontinence episode frequency per day via the 3-day eCRF. A 50% reduction was ...