Clinical trial Recruiting at 1 site Observational Ages 18 to 50 Women only

Diaphragm and breathing muscle differences after childbirth in women with and without diastasis recti

Official title: Diaphragm Characteristics and Respiratory Muscle Function in Parous Women With and Without Diastasis Recti Abdominis

Run by University of Patras · NCT07389993 · Data updated 2026-11-12

This will test whether diaphragm movement and inspiratory muscle strength differ between women who have given birth with and without diastasis recti.

More Diastasis Recti Abdominis (DRA) trials

Quick facts

Study typeObservational
Ages18 Years to 50 Years
SexWomen only
Enrollment42 (estimated)
SponsorUniversity of Patras
Academic / other
Locations1 site (Pátrai, Achaia)
StatusRecruiting
StartedMay 19, 2025
Main results expectedApril 3, 2026
Study endsJuly 10, 2026
Registry record updatedJune 9, 2026
Trial IDNCT07389993 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are parous women aged 18–50 who are at least six months and no more than five years postpartum, can communicate in Greek, and do not have major respiratory, neurological, or connective tissue disorders.

Probably not a fit

Women who are currently pregnant, less than six months postpartum, have severe chronic respiratory disease, connective tissue or neurological disorders, or extensive prior abdominal surgery (other than C-section) are unlikely to benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This cross-sectional observational project compares diaphragm characteristics and accessory inspiratory muscle strength in parous women with and without diastasis recti abdominis. Participants are allocated into two groups based on a standardized imaging assessment of DRA and undergo rehabilitative ultrasound imaging (RUSI) of the diaphragm during specific breathing maneuvers plus inspiratory muscle testing. Eligible participants are women aged 18–50 who are between six months and five years postpartum and able to communicate in Greek, while key exclusions include recent pregnancy, severe respiratory, neurological, or connective tissue disorders, and prior abdominal surgery except cesarean section. All procedures are non-invasive and performed at the Laboratory of Clinical Rehabilitation and Research (CPRlab) at the University of Patras.

Why it matters

Potential benefit: If differences are found, results could guide targeted rehabilitation of the diaphragm and breathing muscles to improve respiratory function and trunk stability after childbirth.

How similar studies have gone: Previous research has explored effects of DRA on pelvic floor and trunk function, but diaphragm-focused investigations are limited and the approach is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Female sex
* Aged 18 to 50 years
* Parous women (at least one previous childbirth)
* At least 6 months postpartum at the time of assessment (and within 5 years postpartum)
* Ability to understand and communicate in Greek
* Willingness to participate and provide informed consent

Exclusion Criteria:

* Current pregnancy
* Delivery within the previous 6 months
* History of severe chronic respiratory disease (e.g., chronic obstructive pulmonary disease, chronic bronchitis, pulmonary emphysema, pulmonary fibrosis)
* Presence of connective tissue disorders
* Presence of neurological disorders
* Severe musculoskeletal conditions that could affect trunk or respiratory function or limit participation in testing procedures (severe low back pain, sciatica etc.)
* Previous abdominal surgery, with the exception of cesarean section

Where it's running

  • Laboratory of Clinical Rehabilitation and Research (CPRlab), University of Patras
    Pátrai, Achaia, Greece
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.