Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Can a phone app replace the clinic for postpartum core recovery?

NCT ID NCT07751952

Disease control Sponsor: Riphah International 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 07, 2026 · Last updated Aug 13, 2026 · Updated 2 times

Summary

This trial tests whether doing core stability exercises via telerehabilitation works as well as in-person physiotherapy for postpartum women with diastasis recti, a condition where abdominal muscles separate. Participants will be randomly assigned to either remote or in-person supervised exercise sessions over 8 weeks. The study measures changes in the gap between abdominal muscles and body image satisfaction.

What this could mean

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

Active substance
Telerehabilitation-based core stability exercise program
What this could lead to
If effective, telerehabilitation could offer a convenient, accessible way for postpartum women to improve abdominal recovery and body image without frequent clinic visits.
What could go wrong
This is a small trial, and results may not apply to all women. The success of telerehabilitation depends on proper remote supervision and adherence, which may vary.

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 54 people

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

Started

Aug 2026

Expected to finish

Dec 2026

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 40 years

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: Participants falling in this category would be recruited into the study. * 6 weeks to 6 months postpartum * Multiparous or primiparous * Diagnosis of diastasis recti (IRD ≥ 2cm)/ * Able to use or operate digital/electronic devices * With internet access and the ability to participate in remote group sessions. Exclusion Criteria: Participants fall in this category would be excluded of the study. * Significant musculoskeletal or systemic comorbidities i.e. diabetes mellitus, cardiovascular disease, Severe psychiatric disorders, Active malignancy. * Prior major abdominal or pelvic surgery (except cesarean) * Any Contraindications to exercise. * Recent/Current pregnancy.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Diastasis recti abdominis (DRA) are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

diastasis recti and weakness of the linea alba puerperal disorder

As listed by the trial registrant

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

Diastasis recti abdominis (DRA) Postpartum

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

  • Lifezone medical and diagnostic center lahore

    RECRUITING

    Lahore, Punjab Province, 0423, Pakistan

More trials for these conditions

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