🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Spain / NCT07639125
Starting soon Not applicable

Effect of Exercise on the Width and Stiffness of the Linea Alba in Postpartum Women With Diastasis

NCT07639125 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2026-06
Last updated
2026-06-10

Condition(s) studied

Diastasis Recti And Weakness Of The Linea Alba

Investigational drug(s) / intervention(s)

Exercise program

Exercise program: Structured therapeutic exercise program aimed at restoring functional integritu of the abdominal-lumbo-pelvic complex over a six week period. The exercise program was based on activation of the transversus abdominis muscle, synergistic co-activation with the pelvic floor muscles, breathing re-education, and the integration of hypopressive abdominal exercises.

Study summary

his study aims to evaluate the effect of an exercise program in postpartum women with diastasis recti, defined as an inter-rectus distance greater than 2 cm at any of three ultrasound measurement points . Participants will be divided into two groups: an intervention group that will follow a 6-week exercise program and a control group that will receive usual care.

Ultrasound assessment of the linea alba will be performed before the intervention and after 6 weeks. The main outcomes will be inter-rectus distance and the stiffness of the linea alba measured using shear wave elastography, along with obstetric and personal clinical variables. Participants will be recruited from primary care centers in the Community of Madrid through midwives during postpartum consultations.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult woman (\> 18 years old) * Women who agreed to participate and provided written informed consent * Women between 6 and 12 weeks postpartum at the time of recruitment. Exclusion Criteria: * History of previous abdominal surgery ( except cesarean section) * Presence of abdominal or umbilical hernias * Current pregnancy * Neuromuscular or systemic conditions affectinf the abdominal wall * Active infections * Any condition that could intervere with the correct execution of the measurement protocol. * Incomplete records or measurements that do not meet elastography quality criteria will be excluded.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Maternatal center Madrid Spain

More University of Vigo trials in Spain

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07639125 on ClinicalTrials.gov ↗ ← All trials in Spain