Nerve Gliding Exercises in Cervical Radiculopathy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-55
SponsorZonguldak Bulent Ecevit University

About this trial

The aim of this study is to investigate the effect of nerve gliding exercises on pain, cervical range of motion, joint position sense, grip strength, functional status and quality of life in individuals with cervical radiculopathy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Have been diagnosed with cervical radiculopathy by a specialist physician

Have disc herniation at the C5-C6, C6-C7 or C7-T1 level according to imaging (magnetic resonance imaging, MRI) findings (in the bulging or protrusion stage)

Have unilateral nerve root involvement

Disqualifiers

Predominance of primary peripheral entrapment neuropathy (carpal/cubital/radial tunnel, etc.)

Multiple nerve root involvement

Progressive neurological deficit

History of trauma or surgery to the cervical and upper extremity region

Trial design

Design model

Parallel

Treatments tested in this trial

  • Convantional rehabilitation

    Other intervention

    This group will have convantional rehabilitation program.

  • Neuromobilization

    Other intervention

    This group will have convantional rehabilitation program and neuromobilization exercises.

Treatment groups

28 Participants
are divided into 2 treatment groups
Group A: Control GroupActive comparator 1 intervention
Group B: Intervention GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Visual Analog Scale (VAS)

The Visual Analog Scale (VAS) will be used to evaluate pain for rest, activity and night periods. The data will be recorded in centimeters.

Time frame
3 weeks

Secondary outcomes

1

Cervical range of motion (CROM)

For CROM, a CROM goniometer will be used to measure cervical flexion, extension, right and left rotation, and right and left lateral flexion movements. The individual will be asked to move to the maximum extent in one direction, and the final position reached will be recorded in degrees.

Time frame
3 weeks
2

Nerve cross-sectional area (CSA)

Will be measured using ultrasound imaging. The results will be recorded in mm².

Time frame
3 weeks
3

Cervical joint position sense

The cervical joint position sense assessment will be performed using the CROM goniometer, targeting 30 and 50 degrees in the directions of flexion, extension, right and left rotation, and right and left lateral flexion. The deviation amount will be calculated by taking the difference between the targeted angle and the position achieved by the individual and will be recorded in degrees.

Time frame
3 weeks
4

Nerve excursion measurement

It will be measured using ultrasound imaging. The results will be recorded in mm.

Time frame
3 weeks.

Other outcomes

Sponsors and contacts

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