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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05812625
Enrollment
68
Registered
2023-04-13
Start date
2023-03-10
Completion date
2023-06-10
Last updated
2023-04-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Radiculopathy

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.

Interventions

Myokinetic stretching technique (MST) is a form of myofascial release, which involves active or passive stretching and movement as well as muscle energy techniques until a desirable release from the taut band is achieved.

OTHERPost Isometric Relaxation

Post Isometric Relaxation (PIR) is the effect of the decrease in muscle tone in a single or group of muscles, after a brief period of submaximal isometric contraction of the same muscle.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Cervical Pain8 weeksCervical Pain will be measured by Numeric Pain Rating Scale
Neck Disability8 weeksNeck disability will be measured by Neck Disability Index
Cervical Range of motion8 weeksCervical Range of motion will be measured by Goniometer

Countries

Pakistan

Contacts

Primary ContactSahreen Anwar, Ph.D
sahreen.anwar@riphahfsd.edu.pk03346591705
Backup ContactMuhammad Talha Hassan Javed, Masters
drtalhahassan97@gmail.com03348196967

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026