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Prone Plank Exercises for Diastasis Rectus Abdominis in Postpartum Women

Prone Plank Exercises Versus Electrical Stimulation in Treatment of Diastasis Rectus Abdominis in Postpartum Women

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06259240
Enrollment
42
Registered
2024-02-14
Start date
2023-03-01
Completion date
2024-04-30
Last updated
2024-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Partum Women

Brief summary

The purpose of this study was to compare between the effects of prone plank exercises versus ES for DRA in postpartum women.

Detailed description

The study conducted on forty-two woman. They had diastasis rectus abdominis12 weeks to 36 months postpartum. They were randomly divided into two equal groups; group A received prone plank exercises while group B recieved electrical stimulation.All patients recieved three sessions per week foe eight weeks.

Interventions

OTHERProne plank exercises

Patients in this group will recieve prone plank exercises, three times a week, for eight weeks, and with a moderate hard intensity. During the first four weeks, the exercises session began with light walking for five minutes followed by corrected exercises. Firstly, women will perform stable prone plank exercises. Secondly, women will be asked to apply the unilateral position of prone plank. Thirdly, using a 65 cm diameter Swiss ball, women will be asked to assume the prone bridge position. During the last four weeks, women will be asked to repeat the same program noting that the progressive prone plank exercises should be applied in a dosage of 20 repetitions, three sets, holding the contraction for one minute, and taking a break for two minutes.

DEVICEElectrical Stimulation

Electrical Stimulation

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* they had DRA 12 weeks to 36 months postpartum, and were referred to physiotherapy by a gynaecologist, multiparous with the IRD measuring greater than two cm. Age ranged between 20-35 years. Body mass index didn't exceed 30 kg/m2.

Exclusion criteria

* they were in ongoing pregnancy, twin pregnancy, premature birth before gestation week 37, and exceeded more than thirty-six months postpartum.

Design outcomes

Primary

MeasureTime frameDescription
Ultrasound Imaging DeviceEight weeks after the beginning of the interventionChanges in Interrectus distance above umbilicus at rest from baseline to four weeks after the beginning of intervention

Secondary

MeasureTime frameDescription
The measuring tapeEight weeks after the beginning of the interventionChanges in waist hip ratio from baseline to four weeks after the beginning of intervention

Countries

Egypt

Contacts

Primary ContactDoaa Salah, Senior
ptdoaasalah@gamil.com20 101 503 3456
Backup ContactFayiz Elshamy, Professor
ff_elshamy@yahoo.com20 109 105 0154

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026