NCT07523906

Brief Summary

The goal of this randomized controlled trial is to compare the effectiveness of lumbar stabilization exercises and muscular chain therapy on reducing pain intensity and functional disability in patients with mechanical CLBP.

  • Participants will be randomly assigned to two groups:
  • Group A: Lumbar stabilization exercises
  • Group B: Muscular chain therapy (posterior sagittal muscle chain) Outcomes will be assessed at baseline and on week 6 to evaluate which exercise program is more effective in reducing pain and improving functional outcomes.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
42

participants targeted

Target at P25-P50 for not_applicable

Timeline
1mo left

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
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 Progress71%
Feb 2026Jun 2026

Study Start

First participant enrolled

February 4, 2026

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

April 5, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

April 13, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 30, 2026

Expected
16 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2026

Last Updated

April 13, 2026

Status Verified

April 1, 2026

Enrollment Period

4 months

First QC Date

April 5, 2026

Last Update Submit

April 5, 2026

Conditions

Keywords

Low Back PainLumbar Stabilization ExercisesMuscular Chain TherapyFunctional Disability

Outcome Measures

Primary Outcomes (2)

  • Pain Intensity

    Pain Intensity will be measured by Numerical Pain Rating Scale

    Assessment will be done at baseline and on Week 6.

  • Functional Disability

    Functional Disability will be assessed using Oswestry Disability Index

    Assessment will be done at baseline and on Week 6

Study Arms (2)

Lumbar Stabilization Exercises

EXPERIMENTAL

Participants will receive lumbar stabilization exercises (Abdominal drawing-in maneuver, Pelvic tilts, Bridging exercise), Repetitions: 10-15 reps per exercise- Sets: 2-3 sets per exercise, Rest Between Sets: 30-45 seconds.

Other: Lumbar Stabilization Exercises

Muscular Chain Therapy

EXPERIMENTAL

1. Straightening the lumbar spine while maintaining hip neutrality and preventing knee flexion. 2. Hip flexion while avoiding lumbar flexion. Static holds: 3-5 repetitions per posture, Hold Duration: 2-3 minutes initially, progressing to 5 minutes ,Rest Interval: 1-2 minutes between repetitions

Other: Muscular Chain Therapy

Interventions

Participants will receive lumbar stabilization exercises (Abdominal drawing-in maneuver, Pelvic tilts, Bridging exercise), Repetitions: 10-15 reps per exercise- Sets: 2-3 sets per exercise, Rest Between Sets: 30-45 seconds.

Lumbar Stabilization Exercises

1. Straightening the lumbar spine while maintaining hip neutrality and preventing knee flexion. 2. Hip flexion while avoiding lumbar flexion. Static holds: 3-5 repetitions per posture, Hold Duration: 2-3 minutes initially, progressing to 5 minutes ,Rest Interval: 1-2 minutes between repetitions

Muscular Chain Therapy

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patients aged between 18-30 years will be included in the study.
  • Participants must have a history of mechanical CLBP.
  • The pain must be localized to the lumbar region.
  • Participants must be able to perform physical activities and participate in exercise-based interventions.
  • Participants who have pain range \> 4 will be included in the study.

You may not qualify if:

  • Patient with structural lesions, such as spondylolisthesis, stenosis, vertebral bone fracture, scoliosis and kyphosis on x-ray, will be excluded.
  • Pregnant females would be excluded.
  • Females with a history of neurological, infections, and systemic disease, including cerebrovascular disease, spondylitis, cancer, spinal cord disease, cauda equine, rheumatologic disorders.
  • Females who have undergone spinal surgery or any surgical intervention related to the lower back or pelvis will be excluded.
  • Lumbar radiculopathy will be excluded in the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Allied Health & Biological Sciences

Islamabad, Pakistan

RECRUITING

MeSH Terms

Conditions

Low Back Pain

Condition Hierarchy (Ancestors)

Back PainPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Muhammad Nazim Farooq, PhD-PT

    Ibadat International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Inza Farooq, MS-PT(MSK)*

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
This randomized controlled trial was double-blinded. Participants were randomly assigned to either the lumbar Stabilization Exercise group or the muscular chain therapy group using a simple randomization (lottery) method. Participants were informed that both interventions were effective physiotherapy treatments for chronic low back pain but were not told which group they belonged to. The outcome assessor, who had over fifteen years of experience, remained blinded to group allocation throughout data collection at baseline and week 6. To maintain blinding, participants were instructed not to disclose their exercise details during assessment, and all data were recorded using coded identifiers (Group A or B).
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 5, 2026

First Posted

April 13, 2026

Study Start

February 4, 2026

Primary Completion (Estimated)

May 30, 2026

Study Completion (Estimated)

June 15, 2026

Last Updated

April 13, 2026

Record last verified: 2026-04

Locations