ClinicalTrials.Veeva

Menu

Effect of Myofascial Release Technique in Patients with Unilateral Cervical Radiculopathy

M

Medipol Health Group

Status

Completed

Conditions

Cervical Radicular Pain
Cervical Disc Herniation
Cervical; Hernia
Cervical Disc Disease
Cervical Radiculopathy
Pain

Treatments

Other: Exercise
Other: Myofascial Release Technique

Study type

Interventional

Funder types

Other

Identifiers

NCT04597112
10840098-604.01.01-E.1062

Details and patient eligibility

About

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).

Enrollment

40 patients

Sex

All

Ages

30 to 65 years old

Volunteers

No Healthy Volunteers

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
  • Migraine
  • Cancer
  • Tumor
  • Osteoporosis
  • Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Myofascial Release Group
Experimental group
Description:
Intervention group, who received conventional therapy and myofascial release therapy.All participants will be given conventional treatment 3 days a week for 4 weeks. Conventional treatment will include 20 minutes hotpack, 5 minutes ultrasound, 20 minutes Transcutaneous Electrical Stimulation. In the intervention group, the myofascial release technique will be applied to the wrist flexors and extensors, elbow flexors and extensors, pectoralis, supraspinatus, infraspinatus, trapezius muscles, starting from the fingers after the conventional treatment, 3 days a week for 4 weeks.
Treatment:
Other: Myofascial Release Technique
Exercise Group
Active Comparator group
Description:
The control group will consist of patients who received conventional therapy and exercise therapy. All participants will be given conventional treatment 3 days a week for 4 weeks. Conventional treatment will include 20 minutes hotpack, 5 minutes ultrasound, 20 minutes Transcutaneous Electrical Stimulation. After conventional treatment, a program consisting of neck extension, lateral flexion and rotation range of motion, stretching of the trapezius muscles and strengthening of the neck extensor muscles will be applied to the control group in the presence of a physiotherapist 3 days a week for 4 weeks.
Treatment:
Other: Exercise

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems