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Cervical Radiculopathy at C5 Nerve RootNCT07429981

Nerve Gliding Exercises in Cervical Radiculopathy

A study testing Convantional rehabilitation and Neuromobilization in people with Cervical Radiculopathy at C5 Nerve Root and Cervical Radiculopathy at C6 Nerve Root, run by Zonguldak Bulent Ecevit University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 55 years
What is being tested?
Convantional rehabilitation and Neuromobilization
Could I receive a placebo?
No, everyone receives an active treatment
How many people
26 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Apr 2026to 20 Jul 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 55 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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

Who cannot join

  • 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
  • Systemic disease contraindicating exercise
  • Pregnancy
  • Manual therapy, injection, or regular physiotherapy applied to the cervical region within the last 3 months
  • Cognitive/psychiatric condition preventing compliance with the assessment protocol

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Zonguldak Ataturk State Hospital

    Zonguldak

Other trials in Turkey (Türkiye)

About this study

Official title: Investigation of the Effectiveness of Nerve Gliding Exercises in Individuals With Cervical Radiculopathy

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.

Read the detailed description

The cervical spine is not only the most mobile region of the spine, but also acts as a functional bridge between the head and the torso, consisting of a total of seven vertebrae. The vertebrae in this region are relatively small in size and have a high capacity for movement due to the need for a wide range of joint motion; these characteristics allow for free movement of the head and enable optimal head-neck positioning in response to environmental stimuli.

Mechanical compression, irritation or inflammation of the cervical nerve roots results in a clinical picture of cervical radiculopathy (broadly defined as cervical neuropathy). This condition presents with symptoms such as pain radiating from the neck to the upper extremities, paraesthesia, muscle weakness and sensory loss. Spondylotic changes in the mobile cervical segments can lead to a decrease in intervertebral disc height, disc protrusion, and degenerative changes in the facet joint capsule.

In cervical radiculopathy, patients may only complain of upper extremity pain; however, they report significant difficulties in functions such as hand-eye coordination, gross and fine grip strength, dressing, and heavy lifting. Indeed, in radiculopathy, in addition to pain and sensory changes, decreased grip strength and reduced upper extremity function are frequently observed findings.

The specific clinical presentations at the root level vary. In C5 root involvement, pain radiates from the end of the cervical level over the shoulder to the upper lateral aspect of the arm; involvement of the deltoid and biceps muscles may cause painful limitation in shoulder abduction and elbow flexion. Degenerative disc disease most commonly affects the C5-6 and C6-7 levels. In C6 root compression, pain starts in the lower part of the neck and extends to the biceps, lateral forearm, and dorsal hand/fingers; it is often accompanied by pain in the proximal arm and sensory deficit in the hand. The most common cause of C7 root radiculopathy is disc herniation; pain in the back of the shoulder and dorsolateral arm with decreased triceps reflex is typical; triceps weakness during overhead activities may be a prominent complaint. The flexor carpi radialis, pronator teres, extensor digitorum communis, and latissimus dorsi may also be affected. The C8 root innervates sensation in the ulnar side of the forearm and hand; compression may cause pain and numbness similar to ulnar nerve lesions. With involvement of the flexor digitorum profundus/superficialis and intrinsic hand muscles, finger flexion and abduction become difficult; weakness of the first dorsal interosseous muscle impairs fine hand skills (e.g., turning a key, holding small objects) and reduces grip strength.

The primary goals of rehabilitation are to reduce pain, preserve nerve function, increase range of motion, and improve quality of life. Among conservative approaches, neural gliding/sliding exercises have gained increasing prominence in recent years. These exercises are targeted manual/exercise-based applications that aim to increase the relative movement of compressed nerve tissue in relation to surrounding tissues; they are reported to improve transmission by reducing intraneural pressure, increase intraneural circulation, and improve the mobility of the connective tissue surrounding the nerve. These mechanisms target pain reduction, increased functional capacity, and improved nerve mobility.

The current literature reports positive effects of nerve gliding exercises on pain, function, and cervical range of motion in cervical radiculopathy. However, most studies have focused on a single peripheral nerve (mostly the median nerve) and applied nerve mobilisation using "one-size-fits-all" protocols independent of the affected root level. This approach carries the risk of overlooking the clinically distinct patterns of radiculopathy that vary according to the root level.

Therefore, our planned study aims to compare the effectiveness of targeted nerve gliding exercises specific to the peripheral nerves (median, ulnar, radial) in cases affected at the C5-C6, C6-C7, and C7-T1 levels. Thus, the effect of nerve mobilisation will be evaluated based on specific nerve-root relationships; determining which nerve mobilisation is more effective at which root level will provide a unique contribution to individualised clinical decision-making processes in the treatment of cervical radiculopathy.

Being tested
Convantional rehabilitation, Neuromobilization
Keywords
Cervical radiculopathy, Neural glide, Neuromobilization
Medical subject headings
Radiculopathy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Convantional rehabilitationOther

    This group will have convantional rehabilitation program.

  • NeuromobilizationOther

    This group will have convantional rehabilitation program and neuromobilization exercises.

Study groups in NCT07429981
Study groupRoleWhat they receive
Control GroupActive comparatorConventional rehabilitation program (isometric neck strengthening exercises, neck stretching exercises) for cervical radiculopathy.
Receives: Other: Convantional rehabilitation
Intervention GroupExperimentalConventional rehabilitation program (isometric neck strengthening exercises, neck stretching exercises) for cervical radiculopathy and neuromobilization exercises.
Receives: Other: Neuromobilization

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: 3 weeks

Secondary outcomes (8)
  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.

    Measured: 3 weeks

  2. Nerve cross-sectional area (CSA)

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

    Measured: 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.

    Measured: 3 weeks

  4. Nerve excursion measurement

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

    Measured: 3 weeks.

  5. Deep cervical flexor muscle endurance

    The endurance of the deep cervical flexor muscles will be assessed using the craniocervical flexion test with the Stabilizer Pressure Biofeedback device. Using the device's feedback, the patient will be asked to perform craniocervical flexion movements starting at 20 mmHg and increasing progressively in 2 mmHg increments up to 30 mmHg. The pressure level at which the individual can successfully hold the position for 10 seconds will be recorded as the activation point, while the number of repetitions at the pressure level at which the patient can hold the position for 10 seconds will be recorded as the performance index.

    Measured: 3 weeks

  6. Gross grip strength

    For gross grip strength measurement, a hydraulic hand dynamometer (Baseline®, USA) will be used. The measurement will be conducted in the standard position specified by the American Society of Hand Therapists. In this position, the individual will sit on a chair with back support, with the elbow at 90 degrees of flexion and the wrist in a neutral position. The person will be asked to squeeze the dynamometer with maximum force. The measurement will be repeated three times, and the average will be recorded in kg/f.

    Measured: 3 weeks

  7. Pinch grip strength

    For pinch grip strength measurement, a mechanical pinch meter (Baseline®, USA) will be used. Lateral (key) pinch, two-point (bipod, tip) pinch, and three point (tripod, palmar) pinch measurements will be performed separately. The measurements will be repeated three times for each side, and the averages will be recorded in kg/f.

    Measured: 3 weeks

  8. Neck Disability Index

    The Neck Disability Index (NDI) is designed to measure neck-specific disability, with the aim of assessing function and quality of life. The questionnaire consists of 10 items related to pain and daily living activities, including personal care, lifting, reading, headaches, concentration, work status, driving, sleep, and leisure. Each item is scored out of five (no disability response is given 0 points) and a total score out of 50 is given for the questionnaire. Higher scores represent greater disability levels. The result will be reported out of 100 by doubling the total score.

    Measured: 3 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Feb 2026
  2. Study start1 Apr 2026
  3. Primary completion1 Jul 2026
  4. Study completion20 Jul 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
26 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07429981
Sponsor's protocol ID
BEUN-AKBAS-3
Status last verified
Feb 2026
First submitted
18 Feb 2026
Last updated
22 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Convantional rehabilitation and Neuromobilization in people with Cervical Radiculopathy at C5 Nerve Root and Cervical Radiculopathy at C6 Nerve Root, run by Zonguldak Bulent Ecevit University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Visual Analog Scale (VAS) (time frame: 3 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Jul 2026.

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