UnknownNot Applicable

Prone Plank Exercises for Diastasis Rectus Abdominis in Postpartum Women

Egypt42 participantsStarted 2023-03-01

Plain-language summary

The purpose of this study was to compare between the effects of prone plank exercises versus ES for DRA in postpartum women.

Who can participate

Age range

20 Years – 35 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * they had DRA 12 weeks to 36 months postpartum, and were referred to physiotherapy by a gynaecologist, multiparous with the IRD measuring greater than two cm. Age ranged between 20-35 years. Body mass index didn't exceed 30 kg/m2. Exclusion Criteria: * they were in ongoing pregnancy, twin pregnancy, premature birth before gestation week 37, and exceeded more than thirty-six months postpartum.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Ultrasound Imaging Device

Timeframe: Eight weeks after the beginning of the intervention

Ultrasound Imaging Device

Timeframe: Eight weeks after the beginning of the intervention

Ultrasound Imaging Device

Timeframe: Eight weeks after the beginning of the intervention

Ultrasound Imaging Device

Timeframe: Eight weeks after the beginning of the intervention

Trial details

NCT IDNCT06259240

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-04-20

Contact for this trial

Doaa Salah, Senior

20 101 503 3456 ptdoaasalah@gamil.com

View on ClinicalTrials.gov More Post Partum Women trials

Who can participate

Age range

20 Years – 35 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Ultrasound Imaging Device

Timeframe: Eight weeks after the beginning of the intervention

Ultrasound Imaging Device

Timeframe: Eight weeks after the beginning of the intervention

Ultrasound Imaging Device

Timeframe: Eight weeks after the beginning of the intervention

Ultrasound Imaging Device

Timeframe: Eight weeks after the beginning of the intervention