About this trial
This study investigates the relationship between diastasis recti abdominis and spinal curvature in postpartum women using non-invasive assessment methods.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age range: 21 to 35 years
BMI between 18 and 29.9 kg/m².
Normal vaginal delivery or cesarean section.
Postpartum period between 6 weeks and 6 months
Disqualifiers
• History of spinal deformities (e.g., scoliosis, kyphosis, spondylolisthesis).
Any neuromuscular or neurological disorders.
Previous abdominal or spinal surgery.
Multiple pregnancies.
Trial population
The study population will include postpartum women who meet the eligibility criteria. Participants will be divided into two groups based on the presence or absence of diastasis recti abdominis and will undergo non-invasive assessment of spinal curvature for comparative analysis.
Trial design
Other
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Lumbar Lordosis Angle
Lumbar lordosis angle measured in degrees in postpartum women with and without diastasis recti abdominis using a non-invasive assessment method.
Locations
Sponsors and contacts
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