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Can a smartphone app replace In-Person therapy for bladder leaks?

NCT ID NCT07597174

Symptom relief Sponsor: Unidade Local de Saúde São João Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compares a mobile app-guided pelvic floor exercise program to standard in-person rehabilitation for women with stress or mixed urinary incontinence. Thirty-two adult women will follow either the app or in-person sessions for 3 months. Researchers will measure changes in quality of life and symptom severity to see if the app is a good alternative.

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-based pelvic floor rehabilitation program
What this could lead to
If it works, this could offer a convenient, at-home alternative to in-person pelvic floor therapy for women with stress urinary incontinence.
What could go wrong
This is a small, early-stage trial with only 32 participants, so results may not apply to everyone. The app may not be as effective as in-person sessions for all women.

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 32 people

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

Started

Mar 2026

Expected to finish

Aug 2026

An estimate. End dates often move.

Lead sponsor

A government agency

The lead sponsor is a government body.

Who can take part

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

Ages

18 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: * age \>18 years * stress urinary incontinence (SUI) or mixed urinary incontinence with predominance of SUI * more than one urinary incontinence episode for week in the last month * pelvic floor muscle strength equal or greater than 2 assessed by Oxford Modified Rating Score Exclusion Criteria: * indwelling urinary catheter * active pelvic neoplasia * pelvic organ prolapse grade greater than or equal to 2 * active urinary tract infection or macroscopic hematuria * neurogenic dysfunction of the lower urinary tract * cognitive deficit, osteoarticular, neurological or psychiatric pathologies that prevent the realization of the therapeutic program * conservative or surgical treatment of UI in the last 12 months * pregnancy or recent childbirth (\< 6 months) * impossibility of access or illiteracy to technological means (smartphone) * unavailability to attend the supervised program due to accessibility, schedule or economic reasons

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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.

Urinary incontinence,stress

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Hospital de São João

    RECRUITING

    Porto, 4200-319, Portugal

More trials for these conditions

Other studies related to the condition(s) this trial covers.