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Comparative Effects of METs and Core Strengthening on Anterior Sacral Torsion Dysfunction

Comparative Effects of Muscle Energy Technique and Core Strengthening on Pain, Sacral Tilt and Disability in Patients With Anterior Sacral Torsion Dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07905118
Enrollment
48
Registered
2026-10-29
Start date
2026-10-22
Completion date
2026-12-31
Last updated
2026-10-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Sacral Torsion Dysfunction

Keywords

Sacral Torsion, METs, SIJD, Core Strengthening, Stretching

Brief summary

This study aims to compare the effects of Muscle Energy Technique (MET) and core strengthening exercises in patients with anterior sacral torsion dysfunction. It will evaluate changes in pain intensity, sacral tilt, and functional disability following the interventions. Participants will be randomly allocated into two groups: Group A will receive MET targeting specific muscles, while Group B will perform core strengthening exercises to improve trunk stability and muscular control. The outcomes will be assessed using the Numeric Pain Rating Scale (NPRS) for pain, smartphone inclinometer for sacral tilt, and Modified Oswestry Disability Index (MODI) for disability. The findings may help determine which intervention is more effective in improving these outcomes in patients with anterior sacral torsion dysfunction.

Interventions

OTHERMETs

Participants will receive MET targeting the piriformis, iliopsoas, and quadratus lumborum muscles.The technique involves positioning the targeted muscle at its restrictive barrier, followed by a gentle isometric contraction against the therapist's resistance for approximately 10 seconds at 20% of maximal voluntary contraction. The muscle is then relaxed, and the therapist gently moves it further into the new range.

Participants will perform core strengthening exercises, including the abdominal drawing-in maneuver, Bridging, Pelvic Tilts alongside the common treatment protocol.

Sponsors

University of Management and Technology Lahore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

Low Back Pain or sacroiliac region pain. Age 20 to 45 years. Both males and females Numeric Pain Rating Scale (NPRS) scoring 3 to 6 at baseline. Pain from at least past three months At least 3/5 positive provocation test for SIJD, Compression Test, Thigh Thrust Test, Sacral Thrust Test, and Gaenslen's Test. A positive Seated Flexion Test, and a negative Standing Flexion were used for the diagnosis of sacroiliac Dysfunction.

Exclusion criteria

Diagnosis of systemic metabolic (DM) and/or neurological disorder (MS, Parkinson or any inflammatory disease Pathological conditions or diagnosed with disk herniation, spinal stenosis, spondylolysthesis, and spondylitis other medical illnesses such as tumor, kidney disease, and visceral disease that can be related with low back pain excluded in this study. Participants who had undergone surgery for LBP. Pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Numeric Pain Rating Scale (NPRS)Baseline and after 6 weeksPain intensity was assessed using the 11-point NPRS, ranging from 0 (no pain) to 10 (worst pain imaginable). It demonstrates good responsiveness in patients with low back pain, with approximately 2 points considered a clinically important change.
Sacral Tilt MeasurementBaseline and after 6 weeksSacral tilt was measured in degrees using a IHandy Level inclinometer, following the landmark-based method of Koumantakis et al. (2016). Three readings were taken in relaxed standing, and their mean was recorded. The same blinded assessor performed measurements at baseline and post-intervention under standardized conditions. Excellent intrarater reliability was reported (ICC = 0.97)
Modified Oswestry Disability Index (MODI)Baseline and after 6 weeksDisability was assessed using the 10-item MODI. Each section is scored from 0 to 5, and the total score is expressed as a percentage. Higher scores indicate greater disability. English and Urdu versions were used according to participants' language preference; appropriate validation references should be cited for both versions.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Oct 30, 2026