Three-dimensional Lumbar Myofascial Release and Motor Control in Lumbar Radiculopathy

Not Applicable

Recruiting

• Conditions: Lumbar Radiculopathy

• Registration Number: NCT06990113
• Lead Sponsor: October 6 University

Brief Summary

to investigate The Efficacy of three-dimensional lumbar myofascial release with motor control training on back perception and pain in lumbar radiculopathy Patients with lumbar radiculopathy demonstrate impairments in function and range of motion to deficits in patient's quality of life.

Detailed Description

PURPOSE: to investigate The Efficacy of three-dimensional lumbar myofascial release with motor control training on back perception and pain in lumbar radiculopathy Patients with lumbar radiculopathy demonstrate impairments in function and range of motion to deficits in patient's quality of life.

HYPOTHESES: It will be hypothesized that there will be no statically Effect of three dimensional lumbar myofascial release with motor control training on back perception and pain in lumbar radiculopathy RESEARCH QUESTION: Is there an Effect of three-dimensional lumbar myofascial release with motor control training on back perception and pain in lumbar radiculopathy

Study Timeline

• Study Start: 2025-04-15
• Status Verified: 2025-05
• Study First Submitted: 2025-05-18
• Study First Submitted QC: 2025-05-18
• Last Update Submitted: 2025-05-18
• Study First Posted: 2025-05-25
• Last Update Posted: 2025-05-25
• Primary Completion: 2025-06-30
• Study Completion: 2025-07-15

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 32

Inclusion Criteria

• Their ages range from 35 to 50 years.
• Both sex
• Unilateral lumbar radiculopathy for more than 6 months.
• Normal body mass index (18.5 - 24.99Kg/m2).

Exclusion Criteria

• • Any other musculoskeletal disorders of the spine or upper extremity

  • Patients with any other Neurological deficits, psychiatric disease lumbar myelopathy, Cognitive problems, vertebral fractures and previous history of spine or lumbar surgery.
  • Clinical instability, recent trauma
  • Structural abnormalities of the spine, osteoporosis, and spasmodic torticollis.
  • Inflammatory or other specific disorders of spina such as ankylosing spondylitis and rheumatoid arthritis

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Fremantle Back Awareness Questionnaire	four weeks	The Fremantle Back Awareness Questionnaire (FreBAQ) has been found to possess adequate psychometric properties in low back pain (LBP) patients worldwide
Oswestry Low Back Pain Disability Questionnaire	four weeks	The Oswestry Disability Index (ODI) a patient-completed questionnaire which gives a subjective percentage score of level of function (disability) in activities of daily living in those rehabilitating from low back pain

Secondary Outcome Measures

Name	Time	Method
pressure pain algometer	four weeks	Algometers are designed to quantify and document levels of tenderness via pressure pain threshold measurement and pain sensitivity via pressure pain tolerance measurement.
visual analog scale	four weeks	The pain VAS is a unidimensional measure of pain intensity, used to record patients' pain progression, or compare pain severity between patients with similar conditions

Trial Locations

Locations (1)

Lama Saad El-Din Mahmoud; 🇪🇬 Al Jīzah, Select State, Egypt