Actively Recruiting

Phase Not Applicable
Age: 20Years - 45Years
All Genders
NCT06598644

Comparison of Sustained Natural Apophyseal Glide &Amp; Instrument Assisted Soft Tissue Mobilization

Led by Riphah International University · Updated on 2025-02-21

56

Participants Needed

1

Research Sites

66 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this randomized controlled trial is to evaluate and compare the effectiveness of two therapeutic techniques-Cervical Sustained Natural Apophyseal Glide (SNAG) and Instrument-Assisted Soft Tissue Mobilization (IASTM)-in the treatment of mechanical neck pain. The trial seeks to determine which method is more effective in reducing pain, improving range of motion, and enhancing overall neck function in individuals suffering from mechanical neck pain.

CONDITIONS

Official Title

Comparison of Sustained Natural Apophyseal Glide &Amp; Instrument Assisted Soft Tissue Mobilization

Who Can Participate

Age: 20Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Both males and females
  • Age between 20 and 45 years
  • History of neck pain lasting longer than 3 months
  • Tenderness on palpation of sternocleidomastoid and levator scapulae muscles
  • Neck pain worsened by turning head to the side
  • Pain score of at least 3 on the Numeric Pain Rating Scale
Not Eligible

You will not qualify if you...

  • Recent injuries or surgeries around the neck
  • Cervical nerve root lesion (radiculopathy)
  • Traumatic injuries such as whiplash
  • Malignancy in or around the neck
  • Rheumatoid arthritis
  • Pregnancy
  • Cervicogenic headache
  • Unwillingness or inability to give informed consent
  • Currently participating in another neck pain treatment program

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Pakistan Railway hospital

Rawalpindi, Punjab Province, Pakistan, 46600

Actively Recruiting

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Research Team

K

KINZA ANWAR, MS-OMPT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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