NCT07848425

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

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
82

participants targeted

Target at P50-P75 for not_applicable

Timeline
2mo left

Started Sep 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

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 Progress26%
Sep 2026Dec 2026

Study Start

First participant enrolled

September 11, 2026

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

September 23, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 30, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 11, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 11, 2026

Last Updated

September 30, 2026

Status Verified

September 1, 2026

Enrollment Period

3 months

First QC Date

September 23, 2026

Last Update Submit

September 23, 2026

Conditions

Keywords

Postpartum females;Sacroiliac joint dysfunction;Postural correction; Lumbar stabilization exercises; Muscle Energy Technique (MET).

Outcome Measures

Primary Outcomes (1)

  • Pain

    Pain measured by VAS

    8 weeks

Study Arms (2)

Muscle Energy Technique (MET)

ACTIVE COMPARATOR
Behavioral: Postural Correction and Lumbar Stabilization ExercisesBehavioral: Muscle Energy Technique (MET)

Postural Correction and Lumbar

EXPERIMENTAL
Behavioral: Postural Correction and Lumbar Stabilization ExercisesBehavioral: Muscle Energy Technique (MET)

Interventions

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.

Muscle Energy Technique (MET)Postural Correction and Lumbar

A manual physiotherapy intervention involving therapist-guided muscle energy techniques to address musculoskeletal dysfunction and improve mobility and functional outcomes in postpartum females.

Muscle Energy Technique (MET)Postural Correction and Lumbar

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersNo
Age GroupsAdult (18-64)

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