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New study tests pelvic floor training for new moms

NCT ID NCT07426770

Prevention Sponsor: Vilnius University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 two approaches to pelvic floor rehabilitation after childbirth: one group works with a specialist using physiotherapy, biofeedback, and electrical stimulation, while the other group trains at home using a mobile app. Researchers want to see if these programs can prevent or reduce pelvic floor issues like incontinence, prolapse, and pain. The study will enroll 80 women and track changes in muscle strength, organ position, and quality of life.

What this could mean

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

Active substance
pelvic floor rehabilitation program (physiotherapy, biofeedback, TENS, and self-training app)
What this could lead to
If successful, this could show that structured postpartum rehabilitation helps prevent or reduce pelvic floor problems like incontinence and prolapse.
What could go wrong
This is a small, early-stage study with 80 participants, so results may not apply to all women. The self-training group may not follow instructions consistently.

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 80 people

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

Started

Jan 2024

Expected to finish

Sep 2029

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

18 to 50 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * 18 years or older * This pregnancy was singleton * No contraindications for physical activity * No connective tissue disorders (for example Ehlers-Danlos syndrome) * No neurological disorders to influence pelvic floor symptoms (for example clinically significant spinal disc herniation) Exclusion Criteria: * Younger than 18 years * Twins or triplet pregnancy * Contraindications for physical activity * Connective tissue disorders * Neurological disorders

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Conditions

The condition(s) this trial relates to.

diastasis recti and weakness of the linea alba pelvic organ prolapse physiological sexual disorder

As listed by the trial registrant

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

Female urinary incontinence and pelvic organ prolapse Pelvic floor dysfunction Postpartum care Postpartum comfort Rectus diastasis Sexual dysfunction female

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

  • Vilnius University: study centers: "Vilnius University Hospital " Santaros Clinic", "Vilniaus Gimdymo Namai"

    RECRUITING

    Vilnius, Lithuania

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