Postural Correction and Lumbar Stabilization vs MET for Postpartum Pain
Effects of Postural Correction Combined With Lumber Stabilization Exercises Versus Muscle Energy Technique in Post-partum Females
1 other identifier
interventional
82
0 countries
N/A
Brief Summary
This randomized clinical trial will evaluate the effectiveness of combined postural correction and lumbar stabilization exercises compared with Muscle Energy Technique (MET) in postpartum women with sacroiliac joint dysfunction following cesarean delivery. The study will include women aged 18-45 years who are 12-48 weeks postpartum and meet the specified clinical criteria for sacroiliac joint dysfunction. A total of 82 participants will be randomly allocated into two groups of 41 participants each. The intervention group will receive postural correction and stabilization exercises, while the comparison group will receive Muscle Energy Technique. Treatment will be provided three times per week for four weeks. Pain intensity, functional disability, and pelvic girdle-related pain and activity limitations will be assessed using the Visual Analogue Scale (VAS), Oswestry Disability Index (ODI), and Pelvic Girdle Questionnaire (PGQ), respectively. Outcomes will be assessed before and after the intervention to determine the comparative effects of the two physiotherapy approaches.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 11, 2026
CompletedFirst Submitted
Initial submission to the registry
September 23, 2026
CompletedFirst Posted
Study publicly available on registry
September 30, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 11, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 11, 2026
September 30, 2026
September 1, 2026
3 months
September 23, 2026
September 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain
Pain measured by VAS
8 weeks
Study Arms (2)
Muscle Energy Technique (MET)
ACTIVE COMPARATORPostural Correction and Lumbar
EXPERIMENTALInterventions
A physiotherapy-based exercise intervention consisting of postural correction strategies and lumbar stabilization exercises designed to improve postural alignment, trunk stability, and functional outcomes in postpartum females.
A manual physiotherapy intervention involving therapist-guided muscle energy techniques to address musculoskeletal dysfunction and improve mobility and functional outcomes in postpartum females.
Eligibility Criteria
You may qualify if:
- Females aged 18-45 years. Postpartum women within the specified postpartum period according to the study protocol.
- Participants who have postpartum low back/pelvic musculoskeletal symptoms relevant to the study.
- Participants who are medically stable and able to participate in physiotherapy. Participants who are able to understand and follow verbal and written instructions.
- Participants willing to participate in the study and provide written informed consent.
You may not qualify if:
- Women with a history of major spinal, pelvic, or lower-limb surgery. Participants with serious spinal pathology, including fracture, malignancy, infection, or severe neurological involvement.
- Participants with severe cardiovascular, neurological, or systemic conditions that contraindicate therapeutic exercise or manual therapy.
- Participants with acute musculoskeletal injury requiring medical/surgical management.
- Participants with pregnancy-related complications requiring specialized medical management.
- Participants currently receiving another structured physiotherapy program targeting the same condition.
- Participants unable to understand or follow the intervention or outcome-assessment procedures.
- Participants who decline or withdraw informed consent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr. Sadaf Anjum
Study Record Dates
First Submitted
September 23, 2026
First Posted
September 30, 2026
Study Start
September 11, 2026
Primary Completion (Estimated)
December 11, 2026
Study Completion (Estimated)
December 11, 2026
Last Updated
September 30, 2026
Record last verified: 2026-09