Efficacy of Hypopressive Exercises Versus Pilates in Women with Abdominal Diastasis in the Postpartum Period: a Randomized Controlled Trial

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity of Alcala

About this trial

The aim of this study is to compare the effects of two exercise programs in women with abdominal diastasis (AD) during the postpartum. One group will receive hypopressive exercises (HE) and the other will receive pilates exercise. The hypothesis of this study is that the execution of both protocols will offer benefits in the ultrasound values of the AD and in the data collected on the quality of life in the short term and 12 weeks after its completion.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Primiparous women over 18 years of age who are within 3 months postpartum.

AD with values >2.5 cm in any of the following reference points: 2 cm supraumbilical or 2 cm infraumbilical.

Vaginal birth.

Disqualifiers

Abdominal or umbilical hernia.

Previous abdominal surgery.

Be receiving any other treatment for your AD

Trial design

Design model

Parallel

Treatments tested in this trial

  • Hypopressive Exercise

    Behavioral

    A hypopressive exercise program will be carry out.

  • Pilates Exercise

    Behavioral

    A pilates exercise program will be carry out.

Treatment groups

48 Participants
are divided into 2 treatment groups
Group A: HE groupExperimental treatment 1 intervention
Group B: Pilates groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Distance between rectus abdominis.

The distance between both muscle bellies of the rectus abdominis will be measured with an ultrasound (linear probe). It will be measured at two reference points: 2 cm supraumbilical and 2 cm infraumbilical.

Time frame
The measurements will be collected at baseline, immediately after the treatment and 12 weeks after the end of treatment.

Secondary outcomes

1

Quality of life

The SF-36 consists of a health questionnaire composed of 36 items for the characterization of a person´s health. The total score ranges between 0 and 100 points. A higher score reflects more optimal health.

Time frame
The scale will be passed at baseline, immediately after the treatment and 12 weeks after the end of treatment.

Other outcomes

Sponsors and contacts

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