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Mobilization With Movement vs. Neural Mobilization on Nerve Root Function in Patients With Cervical Radiculopathy

Not Applicable
Completed
Conditions
Cervical Radiculopathy at C7 Nerve Root
Disc Herniation
Cervical Radiculopathy at C5 Nerve Root
Cervical Radiculopathy
Cervical Radiculopathy at C6 Nerve Root
Interventions
Other: Sustained natural apophyseal glides (SNAGS)
Other: Neural mobilization
Other: Traditional physical therapy
Registration Number
NCT05803954
Lead Sponsor
Cairo University
Brief Summary

This study will be conducted to compare the effect of sustained natural apophyseal glides (SNAGS) versus neural mobilization on clinical outcomes such as 1- nerve root function in the form of: (A) peak to peak amplitude; (B) latency; (C) F wave. 2- pain pressure threshold (PPT) and 3- Neck disability index (NDI) in patients with cervical disc (C5-C6 and/or C6-C7) herniation.

Seventy two patients from both gender with cervical disc (C 5-C 6 and/or C 6- C7) herniation with both sensory and motor nerve affections will be recruited for this study following referral from an experienced neurologist and confirmed diagnosis by MRI. The patients' age will range between 20-50 years, body mass index (BMI) from 18 to 25 kg/cm2.

The patients will be assigned randomly by permuted block to three equal groups; group (A) will receive SNAGS in addition to traditional therapy, group (B) will receive neural mobilization in addition to traditional therapy and group (C) will receive traditional therapy.

peak to peak amplitude, nerve latency and F wave will be measured by electromyography, , pressure pain threshold will be measured by commander algometer. Neck disability will be measured by Arabic neck disability index.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
72
Inclusion Criteria
  1. seventy patients with cervical disc (C 5-C 6 and/or C 6- C7) herniation with both sensory and motor nerve affections, referred from neurologist and confirmed diagnosis by MRI
  2. Both sexes.
  3. Age between 20-50 years.
  4. Patients with neck pain radiating down to the arm.
  5. Patients with positive findings for spurling test, Upper Limb Tension Test One (ULTTO), cervical distraction test and cervical rotation test towards the symptomatic side <60.
  6. BMI from 18 to 25 kg/cm2
  7. Existed active trigger points within middle trapezius and/ or cervical region.
  8. Positive Pittsburgh sleep quality index' value >10, means moderate and/ or sever difficulty.
Exclusion Criteria
  1. Patients experiencing primary shoulder or upper extremity problem of local origin
  2. cardiovascular disorders and respiratory disorders,
  3. pathological conditions involving cervical spine like vertebro basilar insufficiency and canal stenosis
  4. osteophytes in cervical vertebrae
  5. Patients who were undergoing treatment for neck pain with other means of physiotherapy at the time of the study
  6. Cervical fractures, spinal surgery or other spinal pathologies (i.e. ankylosing spondylitis, spondylolisthesis)
  7. Peripheral nerve lesions like neurotmesis and axonotmesis.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Group A (SNAGs group)Traditional physical therapy-
Group A (SNAGs group)Sustained natural apophyseal glides (SNAGS)-
Group B (Neural mobilization group)Traditional physical therapy-
Group B (Neural mobilization group)Neural mobilization-
Group C (traditional physical therapy)Traditional physical therapy-
Primary Outcome Measures
NameTimeMethod
F-wave parametersChange over the course of the study, from baseline to the end of treatment program at 4 weeks

Evaluation of the spinal motoneuron excitability through the measurement of the F wave parameters

Somatosensory Evoked Potentials (SEPs) Latency and AmplitudeChange over the course of the study, from baseline to the end of treatment program at 4 weeks

SEPs are the electrical signals generated by the nervous system in response to somatosensory stimuli. SEPs are read on the skull with electroencephalography (EEG)

Pain pressure threshold by Pressure algometerChange over the course of the study, from baseline to the end of treatment program at 4 weeks

An algometer will be used used to quantify pain intensity by pressure

Secondary Outcome Measures
NameTimeMethod
Neck disability IndexChange over the course of the study, from baseline to the end of treatment program at 4 weeks

Methods of assessment for such disability, especially those targeted at activities of daily living which are most affected by neck pain, questionnaire 10-item scaled entitled the Neck Disability Index (NDI)

Trial Locations

Locations (1)

Ismailia medical complex

🇪🇬

Ismailia, Egypt

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