CompletedNot Applicable

Comparison of Hypopressive Breathing and Noble Technique on DRA in Postpartum Women.

Pakistan50 participantsStarted 2023-02-04

Plain-language summary

The aim of study is to compare the effect of Hypopressive breathing and noble technique on width of Diastasis Recti Abdominis, lumbopelvic pain and maternal functioning in postpartum women.

Who can participate

Age range

24 Years – 45 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: * Multiparous women * History of Cesarean section and vaginal delivery * \> 12 weeks postpartum * Measurement is 2cm or more then 2cm of DRA is included by using finger width palpation and Nylon digital caliper * Lumbopelvic pain (NPRS 3 to 8) Exclusion Criteria: * Exclude women who need surgical correction for DRA * Pelvic organ prolapse * Para umbilical hernia * Malignancy * Bone tuberculosis * Fibromyalgia

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

Modified OSWESTRY Low Back pain Index (ODI)

Timeframe: 12 weeks

IFSAC (Inventory of Functional Status After Childbirth)

Timeframe: 12 weeks

Numeric Pain Rating Scale (NPRS):

Timeframe: 1 day

Trial details

NCT IDNCT05916833

SponsorRiphah International University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-01-01

View on ClinicalTrials.gov More Diastasis Recti Abdominis trials