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Upper Extremity Dysfunction in Patients With Cervical Radiculopathy (CerRad-UE)

U

University of Beykent

Status

Completed

Conditions

Cervical Radiculopathy

Treatments

Other: Observational Assessment Only

Study type

Observational

Funder types

Other

Identifiers

NCT06923085
GO 21/906

Details and patient eligibility

About

This study will examine how cervical radiculopathy (a pinched nerve in the neck) affects function in both arms, not just the symptomatic side. The investigators will evaluate 42 patients with different cervical nerve root involvement (C4-5, C5-6, or C6-7) and compare them to 16 control subjects with non-specific neck pain. The assessments will measure muscle strength, sensory function, hand performance, pain levels, and psychological factors. These evaluations may contribute to the development of rehabilitation programs for cervical radiculopathy.

Enrollment

58 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-65 years
  • Clinical diagnosis of unilateral cervical radiculopathy at C4-5, C5-6, or C6-7 level
  • Diagnosis confirmed by clinical examination and MRI
  • Symptoms present for at least 4 weeks prior to enrollment
  • Ability to understand and follow study instructions
  • Ability to provide informed consent for participation
  • For control group: non-specific neck pain without radiculopathy
  • Ability to complete required assessments

Exclusion criteria

  • Systemic disorders
  • Neurological disorders (excluding CR)
  • Previous spinal surgery
  • Acute trauma
  • Fracture
  • Malignancy
  • Osteoporosis
  • Rheumatic disease
  • Ongoing pharmacological treatment for chronic neck pain

Trial design

58 participants in 4 patient groups

Group 1: C4-5 Radiculopathy Group
Description:
Patients with confirmed C4-5 cervical radiculopathy. Assessments included pain (VAS), neck disability (NDI), upper extremity functionality (DASH), muscle strength measurements, sensory function, hand performance, kinesiophobia (TAMPA) and emotional status (Beck Inventory).
Treatment:
Other: Observational Assessment Only
Group 2: C5-6 Radiculopathy Group
Description:
Patients with confirmed C5-6 cervical radiculopathy. Assessments included pain (VAS), neck disability (NDI), upper extremity functionality (DASH), muscle strength measurements, sensory function, hand performance, kinesiophobia (TAMPA) and emotional status (Beck Inventory).
Treatment:
Other: Observational Assessment Only
Group 3: C6-7 Radiculopathy Group
Description:
Patients with confirmed C6-7 cervical radiculopathy. Assessments included pain (VAS), neck disability (NDI), upper extremity functionality (DASH), muscle strength measurements, sensory function, hand performance, kinesiophobia (TAMPA) and emotional status (Beck Inventory).
Treatment:
Other: Observational Assessment Only
Control Group
Description:
Control subjects with non-specific neck pain without radiculopathy. Assessments included pain (VAS), neck disability (NDI), upper extremity functionality (DASH), muscle strength measurements, sensory function, hand performance, kinesiophobia (TAMPA) and emotional status (Beck Inventory).
Treatment:
Other: Observational Assessment Only

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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