Myo-kinetic Stretching Versus Post-isometrics Relaxation Exercise With Traction in Patients of Cervical Radiculopathy

Not Applicable

Recruiting

• Conditions: Cervical Radiculopathy

• Registration Number: NCT05812625
• Lead Sponsor: Riphah International University

Brief Summary

The goal of this clinical trial is to examine the effectiveness of Myo-kinetic stretching exercises versus post-isometric relaxation exercise in patients with cervical radiculopathy. Convenient sampling technique will be used to enroll the patients. Patients will be screened on the basis of pre formulated eligibility criteria. Written Consent will be taken from each patient for participation in the trial. The calculated Sample size of this study will be 68 calculated through Epitool. Group A will receive conservative baseline treatment consisted of hot pack therapy for 10 minutes and traction for 8 minutes. Myo-kinetic stretching exercises and group B will receive conservative baseline treatment and post-isometric relaxation exercise. The assessment of patients will be done at baseline, 4th and 8th week. The outcomes from patients will be calculated by using Numeric Pain Rating Scale (NPRS), Goniometer and Neck Disability Index. The comparison between pre-treatment and post-treatment data will be done after 8th week. Data will be analyzed through SPSS 25.

Detailed Description

Not available

Study Timeline

• Status Verified: 2023-03
• Study Start: 2023-03-10
• Study First Submitted: 2023-03-31
• Study First Submitted QC: 2023-03-31
• Last Update Submitted: 2023-03-31
• Study First Posted: 2023-04-13
• Last Update Posted: 2023-04-13
• Primary Completion: 2023-05-10
• Study Completion: 2023-06-10

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 68

Inclusion Criteria

• Duration of cervical pain more than 4 weeks.
• History of positive Spurling test

Exclusion Criteria

• History of previous cervical surgery
• Cervical spine tumor.
• Rheumatoid arthritis, prolong steroid use and osteoporosis in cervical region.
• Cervical spine fracture.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Cervical Pain	8 weeks	Cervical Pain will be measured by Numeric Pain Rating Scale
Neck Disability	8 weeks	Neck disability will be measured by Neck Disability Index
Cervical Range of motion	8 weeks	Cervical Range of motion will be measured by Goniometer

Trial Locations

Locations (1)

Allied Hospital; 🇵🇰 Faisalābad, Punjab, Pakistan