Can Local Vibration be Used to Alleviate Symptoms of Cervical Radiculopathy?
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Cervical Radiculopathy
- Sponsor
- Bitlis Eren University
- Enrollment
- 34
- Locations
- 1
- Primary Endpoint
- Paresthesia
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
The aim of this study is to evaluate the effect of local vibration application on the upper extremity pain, paresthesia, neck pain, and limitations in cervical joint range of motion experienced by patients with cervical radiculopathy.
Detailed Description
At least 34 patients diagnosed with cervical radiculopathy who meet the inclusion and exclusion criteria will be included in the study. Subsequently, the patients will be randomly divided into two groups. Patients in the first group will receive placebo local vibration application in addition to conventional treatment, while patients in the second group will receive local vibration application in addition to conventional treatment
Investigators
Omer Dursun
Asst. Prof.
Bitlis Eren University
Eligibility Criteria
Inclusion Criteria
- •Between the ages of 18 and 70,
- •Nerve root compression according to the magnetic resonance imaging,
- •Unilateral or bilateral neck pain rated 3 or higher on the Numeric Pain Rating Scale, or neck pain with paresthesia or upper extremity pain rated 3 or higher on the Numeric Pain Rating Scale.
Exclusion Criteria
- •History of previous cervical or thoracic spinal surgery,
- •Symptoms or signs of upper motor neuron disorder,
- •Body mass index (BMI) higher than 35 kg/m2,
- •Having received spinal injection in the last two weeks,
- •Presence of local infection at the application site,
- •Upper extremity nerve entrapment syndrome (such as carpal tunnel or cubital tunnel syndrome),
- •Diagnosis of systemic inflammatory arthritis (such as rheumatoid arthritis, etc.),
- •Having engaged in strenuous exercise in the last 24 hours,
- •Poor or noncompliance to the treatment program
Outcomes
Primary Outcomes
Paresthesia
Time Frame: Change from baseline neck pain immediately and five days after the intervention
The effect of local vibration intervention on patients' paresthesia will be evaluated using the Patients' Global Impression of Improvement Scale. In this scale, patients will be asked to mark their perceived change in paresthesia using the following options: 'very much better,' 'much better,' 'a little better,' 'no change,' 'a little worse,' 'much worse,' and 'very much worse.'
Neck Pain
Time Frame: Change from baseline neck pain immediately and five days after the intervention
The effect of local vibration intervention on patients' neck pain will be evaluated using the Patients' Global Impression of Improvement Scale. In this scale, patients will be asked to mark their perceived change in pain using the following options: 'very much better,' 'much better,' 'a little better,' 'no change,' 'a little worse,' 'much worse,' and 'very much worse.'
Upper Limb Pain
Time Frame: Change from baseline neck pain immediately and five days after the intervention
The effect of local vibration intervention on patients' upper limb pain will be evaluated using the Patients' Global Impression of Improvement Scale. In this scale, patients will be asked to mark their perceived change in pain using the following options: 'very much better,' 'much better,' 'a little better,' 'no change,' 'a little worse,' 'much worse,' and 'very much worse.'
Secondary Outcomes
- Cervical Range of Motion(Change from baseline neck pain immediately and five days after the intervention)
- The Change in the Pressure Pain Threshold of the Upper Trapezius(Change from baseline neck pain immediately and five days after the intervention)
- The Change in the Viscoelastic Properties of the Upper Trapezius(Change from baseline neck pain immediately and five days after the intervention)