Comparing Pilates and Progressive Prone Plank Exercises to Improve Pain, Strength, and Abdominal Separation in Diastasis Recti in Women
Led by Riphah International University · Updated on 2026-05-08
34
Participants Needed
1
Research Sites
4 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are evaluating the comparative effects of Pilates and progressive prone plank exercises on pain, strength, and the separation of abdominal muscles inter-rectus distance in women diagnosed with Diastasis Recti. This randomized clinical trial focuses on multiparous women with a body mass index under 30 who can safely perform physical activity. The study aims to understand how these two exercise types influence recovery and muscle function in this condition.
Participants will be randomly assigned to one of two exercise groups. Group A will receive Pilates training focused on core activation, controlled breathing, and maintaining neutral spine alignment during mat exercises supervised by a qualified instructor. Group B will follow a progressive prone plank exercise protocol designed to strengthen core muscles important for managing Diastasis Recti, also performed under supervision. Each group will complete 45-minute sessions three times a week for four weeks.
During the study, participants pain levels will be measured using the Numeric Pain Rating Scale, muscle strength via Manual Muscle Testing, and inter-rectus distance by the finger-width method using a Vernier caliper. These assessments will be done before and after the exercise period. Data collected will be analyzed to compare outcomes between the two groups. The total participation period includes these four weeks of exercise and evaluation. Safety and adherence will be monitored throughout the trial.
CONDITIONS
Brief Title
Effects of Pilates and Progressive Prone Plank Exercises in Diastasis Recti
Research Team
I
imran amjad
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Postpartum women within 6 to 12 months after childbirth
Body mass index (BMI) less than 30
Diagnosed with Diastasis Recti with inter-rectus distance of 2 cm or more
Have had either vaginal delivery or cesarean section (C-section)
You will not qualify if you...
Significant pelvic floor dysfunction, pelvic organ prolapse, or related conditions
Unmanaged chronic illnesses such as heart disease or hypertension
Abdominal or related surgeries within the past six months
Currently pregnant or experiencing postpartum complications
Presence of hernia
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Treatment
Duration - 4 weeks
Participants receive supervised Pilates or progressive prone plank exercises focused on core strengthening to manage Diastasis Recti.
Three sessions per week, each lasting approximately 25 minutes
Follow-up
Duration - 1 day
Participants undergo post-treatment evaluations to assess pain, muscle strength, and inter-rectus distance.
1 visit (in-person) after completion of the 4-week treatment
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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