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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05063890
Other study ID # FUI/CTR/2021/6
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2017
Est. completion date January 30, 2019

Study information

Verified date September 2021
Source Foundation University Islamabad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the purpose of this study is to compare the effects of muscle-specific muscle energy technique and movement-specific muscle energy technique in terms of pain, function and cervical range of motion in persons with mechanical neck pain.


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date January 30, 2019
Est. primary completion date January 30, 2019
Accepts healthy volunteers No
Gender All
Age group 19 Years to 44 Years
Eligibility Inclusion Criteria: Mechanical neck pain ranging from 40-80 mm on visual analogue scale (VAS) Age between 19-44 years Pain or limitation on cervical motion - Exclusion Criteria: History of fracture, surgery or trauma in the neck Cervical radiculopathy Myelopathy Spondylosis Syringomyelia Thoracic outlet syndrome Infection Malignancy Inflammatory or rheumatic disorders Vascular syndromes

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Muscle Specific Post Isometric Relaxation MET
3-5 reps of Post Isometric Relaxation MET targeted at muscles of the neck prone to get short
Movement Specific Post Isometric Relaxation MET
3-5 reps of Post Isometric Relaxation MET targeted at specific movements of the cervical spine
unilateral postero-anterior glide
3 sets of unilateral posteroanterior glide (10-15 oscillations) at the involved segment
Heating and TENS
Heating and TENS for 10 minutes

Locations

Country Name City State
Pakistan Foundation University Institute of Rehabilitation Sciences. Islamabad Federal

Sponsors (1)

Lead Sponsor Collaborator
Foundation University Islamabad

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale Pain will be measured using Visual Analogue Scale, with greater score signifying greater pain 5 days
Primary Neck Disability Index Function and neck related disability will be measured using Neck Disability Index, with greater score signifying greater disability and poorer outcome 5 days
Primary Cervical Range of Motion Cervical Range of Motion will be measured using a universal goniometer, with greater score signifying more favorable outcome 5 days
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