Correlation Between Motor Control Dysfunction and Radiographic Parameter in Non Specific Chronic Low Back Pain

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20-40
SponsorMohammad Abdelazeem Darwish Saad

About this trial

This study aims to investigate the relationship between motor control dysfunction (MCD) and radiographic parameters in non-specific chronic low back pain (NSCLBP). Participants will undergo specific clinical motor control tests and lumbar spine X-rays to evaluate the alignment and coordination of spinal and pelvic structures. Understanding this relationship may help improve rehabilitation strategies and reduce pain in affected individuals.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

. Patients diagnosed with non-specific chronic low back pain (NSCLBP) for more than 3 months

Age between 20 and 40 years

Both males and females

Body mass index (BMI) between 18.5 and 29.9

Disqualifiers

• Patients with specific causes of low back pain (e.g., disc herniation, fractures, tumors, infections)

History of spinal or lower limb surgery or injury

Radiculopathy or neurological disorders affecting motor control

Diagnosed spinal deformities (e.g., scoliosis, spondyloarthropathy, ankylosing spondylitis)

Trial population

Patients aged 20-40 years diagnosed with non-specific chronic low back pain (NSCLBP), recruited from the outpatient physical therapy clinic of Cairo University. Participants will be screened based on clinical and radiographic criteria to ensure eligibility and safety.

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

  • Pressure biofeedback assessment

    Diagnostic test

    Participants will be assessed for lumbar motor control using a pressure biofeedback unit (PBU) during the Abdominal Draw-In Maneuver (ADIM) in both crock lying and prone positions. This is a non-invasive test to evaluate deep core muscle function (TrA and MF) in patients with NSCLBP. No therapeutic intervention will be administered.

Treatment groups

64 Participants
are divided into 1 treatment group
Group A: NSCLBP Patients1 intervention

Trial outcomes

Primary outcomes

1

Lumbar Lordotic Angle

Radiographic measurement of the lumbar lordotic angle (LLA) in degrees to assess sagittal spinal alignment in patients diagnosed with non-specific chronic low back pain.

Time frame
At baseline (during initial assessment visit)
2

Pelvic Incidence Angle

Measurement of Pelvic Incidence Angle in degrees obtained from lateral radiographic imaging in patients with non-specific chronic low back pain.

Time frame
At baseline (during initial assessment visit)
3

Pelvic Tilt Angle

Assessment of pelvic tilt angle in degrees as part of the evaluation of lumbopelvic alignment in patients with non-specific chronic low back pain.

Time frame
At baseline (during initial assessment visit)
4

Sacral Slope Angle

Evaluation of sacral slope angle in degrees based on standard radiographic imaging in patients with non-specific chronic low back pain.

Time frame
At baseline (during initial assessment visit)

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Mohammad Abdelazeem Darwish Saad

Lead sponsor

Cairo University

Sponsor institution

This trial is not recruiting at the moment. You can still explore other options: