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Sensory and Functional Impairments in Cervical Disc Herniation

I

Inonu University

Status

Enrolling

Conditions

Cervical Disc Herniation

Treatments

Other: The Visual Analog Scale
Other: Pain Threshold and Tolerance Assessment
Other: Upper extremity functionality
Other: Somatosensory Perception Tests

Study type

Observational

Funder types

Other

Identifiers

NCT07282522
2025/8426

Details and patient eligibility

About

The aim of the study was to evaluate the levels of somatosensory perception, pain threshold and kinesiophobia in individuals with SDH, to examine their relationship with upper extremity functional skills and to compare them with healthy individuals.

Full description

Cervical disc herniation (SDH) occurs when nerve roots and/or spinal cord are compressed due to degeneration or displacement of the cervical intervertebral disc and can present with pain, sensory loss, muscle weakness, and functional limitations. Because the C5-T1 nerve roots provide motor and sensory innervation from the shoulder to the hand, SDH can cause not only pain but also impairments in somatosensory perception, tactile sensations, and proprioceptive awareness. Nerve root compression disrupts the integrity of sensory functions such as touch, vibration, and two-point discrimination, negatively impacting upper extremity abilities. Furthermore, pain and central sensitization processes lower the pain threshold, further limiting motor performance and activities of daily living. Therefore, the combined evaluation of somatosensory perception, pain, and functional abilities in individuals with SDH is crucial for a holistic understanding of the clinical picture.

Enrollment

64 estimated patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria for volunteers in the study: Neck pain lasting at least 3 months, Being between the ages of 18-65 with a diagnosis of cervical disc herniation, Being able to cooperate with the applied parameters, Having good cognitive function, Being literate, Agreeing to participate in the study.

For the control group, having no complaints of neck pain and not having any neck-related diagnosis.

Exclusion criteria for volunteers in the study: Neck pain intensity during activity according to the Visual Analog Scale (VAS) below 3, Individuals who have undergone any surgery related to neck problems, Individuals who have undergone surgery related to upper extremity problems, Individuals with cervical radiculopathy, Having a systemic malignant disease anywhere in the body, Having any disease related to connective tissue or inflammatory rheumatic diseases, Having a psychiatric diagnosis and receiving treatment, Being illiterate, Not having sufficient cognitive function, Having received any neck-related physical therapy in the last 6 months for the CBA group.

Trial design

64 participants in 2 patient groups

Individuals with SDH
Description:
Individuals with SDH are patients diagnosed with cervical disc herniation by a physical therapist.
Treatment:
Other: Upper extremity functionality
Other: Somatosensory Perception Tests
Other: Pain Threshold and Tolerance Assessment
Other: The Visual Analog Scale
healthy participants.
Description:
Individuals with similar demographic characteristics who did not have any neck pain during the initial interview were considered healthy participants.
Treatment:
Other: Upper extremity functionality
Other: Somatosensory Perception Tests
Other: Pain Threshold and Tolerance Assessment
Other: The Visual Analog Scale

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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