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Clinical Trials/NCT06221566
NCT06221566
Completed
Not Applicable

Effectiveness of Muscle Energy Technique (MET) Versus Stretching Exercises In Acute And Subacute Postural Neck Pain. A Randomized Controlled Trial

Dow University of Health Sciences1 site in 1 country40 target enrollmentJuly 13, 2024
ConditionsCervical Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cervical Pain
Sponsor
Dow University of Health Sciences
Enrollment
40
Locations
1
Primary Endpoint
Visual Analog Scale
Status
Completed
Last Updated
last year

Overview

Brief Summary

This study will provide better evidence that which technique is more effective in acute and subacute postural neck pain. To find out the effectiveness of Muscle energy technique (MET) and stretching exercises in acute and subacute postural neck pain.

Detailed Description

Study Design: Randomized Controlled Trial Study Setting: The study will be conducted at the Institute of Physical Medicine and Rehabilitation, Dow University of Health Sciences, Karachi, Pakistan. Intervention: This study will identify effects of two intervention approaches. The Experimental group consists of muscle energy technique (MET) for upper trapezius and levetor scapulae muscle of neck. The Control group will receive a stretching exercises program for upper trapezius and levetor scapulae muscle of neck.

Registry
clinicaltrials.gov
Start Date
July 13, 2024
End Date
November 26, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Targeted population: Students of MBBS, Pharmacy and Doctor of physical therapy.
  • Age between 18 and 30 years
  • Patient having acute or subacute postural neck pain
  • Acute postural neck pain should not last longer than 4weeks
  • Subacute postural neck pain should not last longer than 4-12 weeks.

Exclusion Criteria

  • Cervicogenic headaches
  • Musculoskeletal disorders involve the nerve root compression, i.e.; (Intervertebral disc dysfunction and derangement syndrome)
  • Whiplash associated disorders
  • Fibromyalgia
  • Spinal cord injury
  • Neurological disorders i.e.; (Multiple sclerosis, Young Parkinsonism etc.)

Outcomes

Primary Outcomes

Visual Analog Scale

Time Frame: 03 weeks (1st, 8th, 15th, 21st day)

The pain intensity is measured subjectively on a scale of 0 to 10 cm, where '0 cm' indicates the absence of pain and '10 cm' signifies excruciating pain. Increasing in score suggests worst pain intensity.

Study Sites (1)

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