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Can a video call replace the Doctor's office for pelvic floor training?

NCT ID NCT05443074

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
Running, but no longer taking on new participants.
Completed This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether a remote physiotherapy session works as well as an in-person one for teaching pelvic floor exercises to women with urinary incontinence. 92 women who could not properly contract their pelvic floor muscles were randomly assigned to a face-to-face session, a real-time remote session, or no instruction. The main goal was to see if both teaching methods improved muscle contraction ability equally.

What this could mean

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

Active substance
physiotherapy instruction session
What this could lead to
If successful, this could show that remote instruction is as effective as in-person sessions, making pelvic floor therapy more accessible.
What could go wrong
This is a small, completed study (92 participants) comparing teaching methods, not testing a new treatment. Results may not apply to all women or settings.

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

92 people

The number who actually took part.

Started

Apr 2023

Finished

Sep 2025

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 90 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: * Women who are not able to contract their PFM (≤ 2 of Modified Oxford Scale); * Cognitive ability, hearing and visual acuity preserved (through 10-point cognitive screener and Snellen test, respectively); * Non-neurogenic UI; * No history of neurological disorders; * No symptoms of a vaginal or urinary tract infection; * Pelvic organ prolapse ≤2 (according to the Baden and Walker scale); * Who have not already been instructed on how to perform PFM contraction or who is not already performing PFM training; * No suspected or confirmed pregnancy. Exclusion Criteria: * Who have intolerance to physical examination, or latex allergy; * Who withdraws from participating in the study.

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Conditions

The condition(s) this trial relates to.

Urinary Incontinence

As listed by the trial registrant

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

Contacts and locations

Locations

  • University of São Paulo

    Ribeirão Preto, São Paulo, 14026956, Brazil

More trials for these conditions

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