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Clinical Trials/NCT07329478
NCT07329478
Recruiting
Not Applicable

Effects of Muscle Specific as Compared to Movement Specific Muscle Energy Technique on Isometric Muscle Strength and Muscular Endurance in Individuals With Mechanical Neck Pain

Foundation University Islamabad1 site in 1 country30 target enrollmentStarted: January 15, 2025Last updated:

Overview

Phase
Not Applicable
Status
Recruiting
Enrollment
30
Locations
1
Primary Endpoint
Pain Intensity

Overview

Brief Summary

Neck pain, prevalent in young adults due to poor posture, sedentary habits, and muscle imbalance. This study aims to compare the effects of muscle-specific versus movement-specific MET on pain, isometric muscle strength, and endurance of neck flexors and extensors. Pre- and post-intervention assessments using VAS, Modified Sphygmomanometer Dynamometer, and cranio-cervical flexion/extension tests will evaluate treatment outcomes.

Detailed Description

Neck pain, affecting nearly 75.7% of young adults, is commonly linked to poor posture, sedentary lifestyles, and muscle imbalances. If left untreated, it may lead to disability and degenerative changes. Among rehabilitation approaches, muscle energy techniques (METs) have shown effectiveness in improving pain, mobility, and function by targeting neuromuscular dysfunction. This study aims to compare the effects of muscle- specific MET with movement-specific MET on pain, isometric muscle strength, and muscular endurance of neck flexors and extensors in individuals with neck pain. A randomized control trial will be conducted using purposive sampling. Thirty participants will be divided into two groups: Group A (movement-specific MET) and Group B (muscle-specific MET), with both groups following a standard protocol of Tens and Hotpack applied for 10 mins proceeding every session for five sessions.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Masking Description

assessor will be blind

Eligibility Criteria

Ages
19 Years to 44 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age 19-44 years.
  • Both Genders (Male and Female).
  • Limitation on cervical motion
  • Pain ranging from 40-80 mm on visual analogue scale (VAS)

Exclusion Criteria

  • Participants with a positive history of fracture, surgery or trauma in the neck region, thoracic outlet syndrome, infection, any malignancy.
  • Vascular syndromes such as vertebrobasilar insufficiency.
  • Inflammatory, or rheumatic disorders, cervical radiculopathy, myelopathy, spondylosis, or syringomyelia.

Outcomes

Primary Outcomes

Pain Intensity

Time Frame: 5 days

Visual Analog Scale will be used for measuring pain intensity, 0 is no pain and 10 is worst pain.

Isometric muscle strength

Time Frame: 5 days

Modified Sphygmomanometer Dynamometer will be used to measure isometric muscle strength. In which Higher pressure is stronger muscles; lower values suggest weakness or dysfunction.

Muscle endurance

Time Frame: 5 days

Cranio-cervical flexion Test/ Cranio-cervical extension Test will be used for measuring muscle endurance. Strong contraction means normal; weakness suggests flexors/extensors' dysfunction.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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