Efficacy of Hypopressive Exercises Versus Pilates in Women with Abdominal Diastasis in the Postpartum Period: a Randomized Controlled Trial (AD-HE-PI)

University of Alcala

Status: Not yet enrolling

Conditions: Abdominal Diastasis

Treatments: Behavioral: Hypopressive Exercise; Behavioral: Pilates Exercise

Study type: Interventional

Funder types: Other

Identifiers

NCT06599541

Abdominal diastasis

Details and patient eligibility

About

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.

Full description

Objective: To compare the efficacy of hypopressive exercises (HE) versus pilates exercise in women with abdominal diastasis (AD) during the postpartum, and to know the effects of each of the exercises independently.

Design: Single-blind randomized controlled trial.

Setting: Faculty of Physical Therapy of Alcalá de Henares (UAH).

Participants: Primiparous women with DA who have vaginal delivery and are in the 3 months postpartum (N=40).

Interventions: Participants will be randomly assigned to perform either a HE program focused on freediving work (n=20) or a pilates program focused on exhalation (n=20). The intervention will consist of 3 weekly sessions lasting 30 minutes over 12 weeks, where they will receive a weekly face-to-face and group session and two home sessions.

Main outcome measures: The primary outcome will be measurement of the distance between rectus abdominis through ultrasound to be assessed at baseline, immediately after the intervention and 12 weeks later. The secondary outcome measure will correspond to the measurement of quality of life using the SF-36 Health Questionnaire. It will be collected through masked evaluations by 2 physiotherapists at baseline, at the end of the intervention and at 12 weeks.

Enrollment: 48 estimated patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 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.

Exclusion criteria

• Abdominal or umbilical hernia.
• Previous abdominal surgery.
• Be receiving any other treatment for your AD

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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48 participants in 2 patient groups

HE group

Experimental group

Description:

Participants with AD who are going to perform hypopressive exercises

Treatment:

Behavioral: Hypopressive Exercise

Pilates group

Experimental group

Description:

Participants with AD who are going to perform pilates exercises.

Treatment:

Behavioral: Pilates Exercise