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Comparison of the immediate effects of rehabilitation manual techniques on motor control in Non- Specific Chronic Low Back Pain through EMG activities in lumbopelvic muscles and flexion-relaxation phenomenon.

Comparison of the immediate effects of rehabilitation manual techniques on motor control in Non- Specific Chronic Low Back Pain through EMG activities in lumbopelvic muscles and flexion-relaxation phenomenon

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090301001722N22
Enrollment
39
Registered
2019-12-10
Start date
2019-12-11
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Non-Specific Chronic Low Back Pain. Low back pain

Interventions

Intervention 1: Control group: Based on methodology, EMG would be performed on this healthy group without performing any treatment. Intervention 2: Intervention group: Spinal Manipulation Technique. I

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Men patients aged between (20 – 60) years old. 2. NS-CLBP repeated or continued for a minimum period of 3 months duration.3. The presence of localized pain in the lower back (pain in the area from 12th to gluteal folds) without pain referral or radicular into the lower extremities.4. Moderate pain =Numeric pain scale 5 to 7/10.5. No severe pathology or the absence of “red flags” (specific causes of LBP such as cauda equine syndrome or inflammatory disease).6. Pain/symptom provocation on static, one-sided loading and/or more specific activities/postures (e.g. desktop-workers, car driver...), whereas dynamic (low load) exercises/activities result in pain reduction and/or functional improvement.

Exclusion criteria

Exclusion criteria: The presence of non-mechanical pain generalized pain on a specific function, such as the diagnosis of (eg, spinal canal stenosis, spondylolisthesis, spinal fracture, acute inflammatory diseases, hemorrhagic diseases, active tuberculosis, and recent deep vein thrombosis).Had overt neurological signs (sensory deficits or motor paralysis).Had diagnosed spinal deformities or previous spine surgery.Any problems in hips (i.e. fractures, dislocations), knee (i.e. paresthesia below the knee) and ankle (i.e. ankle instability).Systemic diseases (diabetes, tumors).

Design outcomes

Primary

MeasureTime frame
PAIN. Timepoint: Before & after Treatment. Method of measurement: Numeric Pain Rating Scale (NPRS).;Beta-band intermuscular coherence. Timepoint: Before & after Treatment. Method of measurement: Surface EMG by Biometrics (Ltd) data Log.;Flexion-relaxation phenomena. Timepoint: Before & after Treatment. Method of measurement: Surface EMG by Biometrics (Ltd) data Log.;Muscles activity. Timepoint: Before & after Treatment. Method of measurement: Surface EMG by Biometrics (Ltd) data Log.

Secondary

MeasureTime frame
Disability. Timepoint: Before & after Treatment. Method of measurement: Oswestry Low-Back Pain Disability Index (ODI).;Fear-Avoidance Beliefs. Timepoint: Before & after Treatment. Method of measurement: Fear-Avoidance Beliefs Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Mohammad-Reza Hadian Rasanani

Tehran University of Medical Sciences

hadianrs@sina.tums.ac.ir+98 21 8891 3469

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026