Effects of Innominate Rotation Correction Compared With Sacral Torsion Correction in Patients With Sacroiliac Joint Dysfunction
1 other identifier
interventional
50
1 country
1
Brief Summary
The purpose of this study is to evaluate the comparative effects of Innominate Rotation Correction and Sacral Torsion Correction using Muscle Energy Techniques (METs) in patients with Sacroiliac Joint Dysfunction (SIJD). A total of 50 participants will be recruited, aged 18-50 yrs, with confirmed SIJD based on atleast 3 positive provocation tests. Participants will be randomized into two equal groups. Group A (Innominate Rotation Correction) and Group B (Sacral Torsion Correction). Both groups will receive Conventional Therapy (Thermotherapy, Electrotherapy and Core stabilization exercises). Study variables include:
- Independent Variable: Type of MET applied (Innominate vs Sacral Torsion)
- Dependent Variables: Pain (measured by Visual Analog Scale), Functional Disability (assessed via Denver SIJ Disability Questionnaire)
- Control Variables: Age, Gender, BMI, Baseline Pain/ Disability Scores The intervention will last 4 weeks with 8 sessions (2 sessions per week). Assessments will be conducted at baseline (Week 1, Pre-treatment) and Post every second session. Data will be analyzed to compare immediate and short-term effects of the two interventions. This study aims to provide evidence for targeted manual therapy approaches in SIJD, potentially guiding clinicians toward the most effective technique for pain reduction and functional improvement.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Dec 2025
Shorter than P25 for not_applicable
1 active site
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
First Submitted
Initial submission to the registry
September 9, 2025
CompletedFirst Posted
Study publicly available on registry
September 16, 2025
CompletedStudy Start
First participant enrolled
December 30, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
June 1, 2026
January 2, 2026
September 1, 2025
5 months
September 9, 2025
December 26, 2025
Conditions
Outcome Measures
Primary Outcomes (2)
JOINT DISABILITY
The Denver Sacroiliac Joint Disability Questionnaire (DSIJQ) comprises 10 items that assess various aspects of SIJ-related disability, including pain intensity, mobility, self-care, and social participation. Each item is scored on a 6-point Likert scale ranging from 0 to 5. (0 - No Disability; 5 - Unable to perform activity). To calculate the total percentage, the obtained score is divided by 50 and multiplied by 100 to calculate total percentage. Then it is compared with an Ordinal Scale grading, shown as follows: * 0-20% = Minimal Disability * 21-40% = Moderate Disability * 41-60% = Severe Disability * 61-80% = Crippled * 81-100% = Bed-bound or Exaggerating symptoms
Before and After 4 weeks.
JOINT PAIN
The Visual Analog Scale (VAS) is a simple patient-reported measure of current Pain Intensity. Scoring - Patients mark their pain on a 10-cm horizontal line, anchored by "No Pain" (0-cm) and "Worst Possible Pain" (10-cm), and the distance between 0-cm to the Point of Pain perception is marked as the recorded score (in millimeters or centimeters). High Value means Severe Pain and vice versa.
Before Treatment and After 4 weeks
Study Arms (2)
Group A: Sacral Torsion Correction
ACTIVE COMPARATORParticipants allocated to this arm will receive Muscle Energy Techniques (METs) for Sacral Torsion Correction. Covering Patterns: * Left-on-Left Torsion * Right-on-Right Torsion * Left-on-Right Torsion * Right-on-Left Torsion * Bilateral Nutation * Bilateral Counternutation Each participant will undergo 8 sessions over 4 weeks (2 Sessions/week), and receive Conventional Physiotherapy
Group B: Innominate Rotation Correction
EXPERIMENTALParticipants allocated to this arm will receive Muscle Energy Techniques (METs) for Innominate Rotation Correction along with Conventional Treatment. * Anterior Rotation * Posterior Rotation Each participant will undergo 8 Sessions over a period of 4 weeks (2 Sessions/week).
Interventions
Conventional management including Electrotherapy by application of Thermotherapy or Cryotherapy, Transcutaneous Electrical Nerve Stimulation (TENS) for 20 minutes, Core-stabilization Exercises, * Clamshells * Four Point Kneeling * Bridging/Side Bridges * Bird-Dog Pose * Dead Bugs * Dynamic Core Stability (Unstable Surfaces) For Sacral Torsions, Six MET protocols address Forward and Backward torsions on Left and Right Oblique axis using patient generated force in Prone or Side-lying positions. Left-on-Left (LOL) Forward Torsion, Right -on-Right (ROR) Forward Torsion, Right-On-Left (ROL) Backward Torsion, Left-on-Right (LOR) Backward Torsion, Bilateral Sacral Nutation, Bilateral Sacral Counternutation
Conventional management including Electrotherapy by application of Thermotherapy or Cryotherapy, Transcutaneous Electrical Nerve Stimulation (TENS) for 20 minutes, Core-stabilization Exercises, • Clamshells • Four Point Kneeling • Bridging/Side Bridges • Bird-Dog Pose • Dead Bugs • Dynamic Core Stability (Unstable Surfaces). Anterior Innominate Rotation and Posterior Innominate Rotation.
Eligibility Criteria
You may qualify if:
- Dysfunction based on at least 3 of the following tests
- Distraction Test
- Compression Test
- Gaenslen's Test
- Thigh Thrust Test
- Sacral Thrust Test
- Presence of Pain in Buttock, Posterior Pelvis, or Lower Lumbar Region for more than 2 weeks
- Confirmed Pelvic Asymmetry through Palpation (i.e., ASIS/PSIS Landmarks, Gillet's Test)
You may not qualify if:
- History of Lumbar or Pelvic Fracture, Recent Surgery, or Hip/Knee Pathology affecting Gait/Posture.
- Pregnancy or Post-partum less than 6 months - due to Hormonal Laxity \& Altered Biomechanics
- Systemic Inflammatory conditions - Rheumatoid Arthritis, Ankylosing Spondylitis
- Neurological Deficits - Cauda Equina Syndrome, Radiculopathy with Motor Loss
- Ongoing Physiotherapy treatment for Low Back Pain in past 4 weeks
- Inability/Contraindications to tolerate Manual Therapy - Osteoporosis
- Leg Length Discrepancy - \>1.5 cm or Structural Scoliosis
- BMI \> 35 (ASIA) - it may affect assessment validity due to obesity
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Foundation University College of Physical Therapy
Islamabad, Punjab Province, 46000, Pakistan
Study Officials
- PRINCIPAL INVESTIGATOR
Muhammad Shafay Ali, DPT
Foundation University Islamabad
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 9, 2025
First Posted
September 16, 2025
Study Start
December 30, 2025
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
June 1, 2026
Last Updated
January 2, 2026
Record last verified: 2025-09