Effectiveness of Muscle Energy Technique (MET) Versus Stretching Exercises In Acute And Subacute Postural Neck Pain

December 10, 2024 updated by: Dow University of Health Sciences

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

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.

Study Overview

Status

Completed

Conditions

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.

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Sindh
      • Karachi, Sindh, Pakistan
        • Nida Naqi

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

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.)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group A
Muscle energy technique (MET)

Muscle energy technique (MET) for upper trapezius and levetor scapulae muscle of neck with 7 to 10 second hold, 3 to 5 repetitions.

Transcutaneous electrical nerve stimulation (TENS) with Cold pack.

Home exercise program (HEP) will receive by both the groups which will be not supervised by the principal investigator or any other investigator.

Active Comparator: Group B
Stretching exercise program

Stretching exercises program for upper trapezius and levetor scapulae muscle of neck with 10 second hold, 15 repetitions.

Transcutaneous electrical nerve stimulation (TENS) with Cold pack.

Home exercise program (HEP) will receive by both the groups which will be not supervised by the principal investigator or any other investigator.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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.
03 weeks (1st, 8th, 15th, 21st day)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: NIDA NAQI, MSAPT, Dow University of Health Sciences

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 13, 2024

Primary Completion (Actual)

November 26, 2024

Study Completion (Actual)

November 26, 2024

Study Registration Dates

First Submitted

January 6, 2024

First Submitted That Met QC Criteria

January 22, 2024

First Posted (Actual)

January 24, 2024

Study Record Updates

Last Update Posted (Estimated)

December 13, 2024

Last Update Submitted That Met QC Criteria

December 10, 2024

Last Verified

December 1, 2023

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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