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NCT Number: NCT07639125

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

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.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Maternatal center

Madrid, Spain

Location contact

Sara Cañamero de León, Midwife

CONTACT

[email protected]

+34 ext. +3910 83 37 58

About this study

In this study, the effect of an exercise program on postpartum women with diastasis will be evaluated. Diastasis will be defined as an inter-rectus distance greater than 2 cm at any of the points assessed by ultrasound (5 cm above the navel, at the level of the navel, and 2 cm below the navel).

Participants will be divided into two groups: one group will receive an exercise program for 6 weeks, while the other group will serve as the control group, receiving usual care. An ultrasound assessment of the linea alba will be performed before the start of the study and after 6 weeks.

The main variables evaluated will be inter-rectus distance and the stiffness of the linea alba measured by shear wave elastography, in addition to obstetric and personal variables obtained from the medical history. Participants will be recruited from primary care centers in the Community of Madrid through midwives during postpartum consultations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

exercise program

Other

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.

Other names: exercise therapy

Primary outcomes

  1. Interrectus distance

    Time frame: From enrollment to the end of treatment at 6 weeks.

    This group does not follow the exercise program and continues with their usual care through the public healthcare system, which does not include any intervention for diastasis.

  2. Stiffness of the linea Alba

    Time frame: From enrollment to the end of treatment at 6 weeks.

    CopilotThe stiffness of the linea alba will be measured at three points (5 cm above the navel, at the level of the navel, and 2 cm below the navel) using shear wave elastography.

Study contacts

Contact information is provided by the study sponsor or research team.

Iria Da Cuña Carrera, Physiotherapy

CONTACT

[email protected]

+34 986801750

Sponsors and collaborators

Lead sponsor

University of Vigo

Other

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 10, 2026
Registry last updated
Jun 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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