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Clinical Trials/NCT04597112
NCT04597112
Completed
Not Applicable

Effect of Myofascial Release Technique in Patients with Unilateral Cervical Radiculopathy

Istanbul Medipol University Hospital1 site in 1 country40 target enrollmentOctober 13, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cervical Radiculopathy
Sponsor
Istanbul Medipol University Hospital
Enrollment
40
Locations
1
Primary Endpoint
Myometer
Status
Completed
Last Updated
last year

Overview

Brief Summary

The aim of the study is to investigate the effectiveness of myofascial release technique on pain, range of motion, muscle strength, functionality and quality of life in individuals diagnosed with cervical radiculopathy with unilateral arm involvement and compare this with exercise. The individuals included in the study will be randomized into two groups, 17 control and 17 study groups. Sessions will be 3 days a week for 4 weeks. Conventional physiotherapy and exercise program will be applied to the control group, conventional physiotherapy and myofascial release technique will be applied in the intervention group. Conventional physiotherapy methods; It will include Transcutaneous Electrical Nerve Stimulation (TENS), Ultrasound (US), hotpack agents. Exercise program; extension, right and left lateral flexion, right and left rotation exercises, chin-tuck, right and left upper trapezius muscle group stretching, neck extensor muscle group isometric strengthening exercises. Myofascial release will be applied to the fingers, wrist flexor-extensor muscle groups, elbow flexor-extensor muscle groups, pectoral muscles and rotator cuff muscle groups. Patients will be evaluated before and after treatment with Visual Analogue Scale (VAS), Goniometric measurements, algometer, myometer, Neck Disability Scale, "Disability of Arm, Shoulder and Hand" Questionnaire (DASH).

Registry
clinicaltrials.gov
Start Date
October 13, 2020
End Date
June 1, 2021
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Istanbul Medipol University Hospital
Responsible Party
Principal Investigator
Principal Investigator

fatih bali

Lecturer

Istanbul Kent University

Eligibility Criteria

Inclusion Criteria

  • Getting a diagnosis of cervical radiculopathy
  • Unilateral upper extremity symptoms at least for a month
  • The diagnosis is confirmed by the medical board report
  • Being between the ages of 30-65
  • Voluntary acceptance to participate in the study

Exclusion Criteria

  • Previous cervical surgery
  • Previous cervical trauma
  • Have had myofascial therapy or conventional therapy for cervical radiculopathy
  • Long-term use of corticosteroids
  • Congenital torticollis history
  • Using nonsteroidal anti-inflammatory drugs for long time
  • Osteoporosis
  • Pregnancy

Outcomes

Primary Outcomes

Myometer

Time Frame: 10 minutes

Hand myometer is a means of expressing force quantitatively. It is preferred over other dynamometers because of its ease of use and portability.

Algometer

Time Frame: 10 minutes

It is a device used to evaluate the sensitivity to pain and to determine the perception of pressure. The pressure algometer has proven useful in evaluating fibrositis and hypersensitive spots, trigger points, arthritis activation, and visceral pain-pressure sensitivity.

Visual Analog Scale

Time Frame: 1 minutes

Visual Analog Scale (VAS) is used to convert some values that cannot be measured numerically into digital. Two end definitions of the parameter to be evaluated are written on both ends of a 100 mm line and the patient is asked to indicate where his / her condition is appropriate by drawing a line or by placing a dot or marking.

Electrogoniometer

Time Frame: 10 minutes

It is an evaluation tool used to record the objective measurement of joint range of motion.

Secondary Outcomes

  • Neck Disability Index(10 minutes)
  • Disability of Arm Shoulder and Hand Test(10 minutes)

Study Sites (1)

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