Chronic non-specific low back pain. Low back pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with non-specific chronic low back pain (NSCLBP) with duration of more than 3 months (=12 weeks). Age between 18 and 70 years. Presence of mechanical low back dysfunction based on clinical assessment. Presence of at least one tender point in the iliopsoas muscle (unilateral or bilateral). Absence of relevant lateral shift.
Exclusion criteria
Exclusion criteria: Loss or absence of Directional Preference (DP) in the initial assessment Skin infection in the groin area. Acute iliopsoas injury (hematoma or acute strain). History of inguinal hernia repair with mesh. Pelvic visceral disorders. History of pelvic surgery. Pregnancy at the time of the study. Fracture, tumor, inflammatory or infectious diseases of the spine. Evidence of nerve root involvement (radiculopathy) such as muscle weakness, reflex changes, or sensory deficits in the lower extremities. History of lumbar spine surgery. Lumbar spinal fusion. Bowel or bladder incontinence, or saddle anesthesia (symptoms of Cauda Equina Syndrome). Cognitive impairment or inability to communicate effectively. Unwillingness to continue participation in the study. Inability to read and write.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Directional Preference status, Directional Preference status is categorized into three groups: stable (direction remains the same before and after treatment), changed (direction changes after treatment), or newly developed (directional preference appears after treatment). Timepoint: before the intervention (baseline) and after completion of three treatment sessions (post-intervention). Method of measurement: Assessed using the standards McKenzie Lumbar Assessment Form by a certified McKenzie therapist. Directional preference is determined based on the patient's response to repeated movements in different directions. | — |
Secondary
| Measure | Time frame |
|---|---|
| Intensity and quality of pain. Timepoint: Before intervention and after three treatment sessions. Method of measurement: Short-Form McGill Pain Questionnaire (SF-MPQ).;Flexion and extension range of motion of the lumbar spine. Timepoint: Before intervention and after three treatment sessions. Method of measurement: Using TiltMeter smartphone application installed on an iPhone. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tehran University of Medical Sciences