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Can a smartphone app help older women stop leaking urine?

NCT ID NCT07427693

Symptom relief Sponsor: Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a mobile app and a connected device can help women aged 55 and older with stress urinary incontinence do pelvic floor exercises at home. The app guides exercises and provides feedback on muscle contractions. The goal is to see if this approach reduces leaks and improves quality of life. The study is small with 36 participants and is not yet recruiting.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
mobile app and connected Bluetooth dynamometer for pelvic floor muscle training
What this could lead to
If it works, this could offer a convenient, at-home option to reduce urinary leaks and improve quality of life for older women.
What could go wrong
This is a small, early-stage study with only 36 participants, so results may not apply widely. The app and device may be hard to use for some, and benefits may be modest.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 36 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2025

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

55 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Women * 55 years + * Stress or mixed UI symptoms with predominantly stress UI symptoms * At least 3 or more urinary leaks/week * Able to ambulate safely * Understand simple instruction in French, written and verbally * Basic understanding of how to use a tablet or mobile phone * Willing to participate in a gynecological exam * Able to properly contract the PFM * Provide informed consent. Exclusion Criteria: * Urge UI symptoms or mixed incontinence with primarily urgency * Neurological condition * Grade 3 or 4 of pelvic organ prolapse (POP) * Any other acute or chronic condition likely to interfere with the mobile app and/or connected object * Risk factors likely to interfere with the mobile app and/or connected object (i.e.: chronic constipation, chronic cough) * Medications that can interfere with the mobile app and/or connected object * Received UI treatments in the last year.

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Conditions

The condition(s) this trial relates to.

female stress incontinence Urinary Incontinence Urinary Incontinence, Stress

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Telehealth Urinary incontinence (UI) Urinary stress incontinence

Contacts and locations

Locations

  • Women's Health and Aging Laboratory - CRIUGM

    Montreal, Quebec, H3W 1W4, Canada

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