Actively Recruiting

Phase Not Applicable
Age: 18Years - 30Years
All Genders
NCT07444112

Effect of Myofascial Release Therapy on University Students With Text Neck Syndrome.

Led by University of Health Sciences Lahore · Updated on 2026-03-02

62

Participants Needed

2

Research Sites

6 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized controlled trial aims to determine the effectiveness of myofascial release therapy in university students with text neck syndrome as prolonged smartphone and digital gadgets use has been associated with neck pain, forward head posture, and increased perceived stress among young adults with screen time more than 3 hours. Participants will be randomly allocated into control group and intervention group and will be treated for 4 weeks. Clinical outcomes including neck pain, neck pain intensity, craniovertebral angle for posture assessment, and perceived stress levels will be measured at baseline and post-intervention. The study seeks to determine whether Myofascial Release Therapy acts as a non-invasive technique in improving musculoskeletal and psychosocial parameters related to text neck.

CONDITIONS

Official Title

Effect of Myofascial Release Therapy on University Students With Text Neck Syndrome.

Who Can Participate

Age: 18Years - 30Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • University students aged 18 to 30 years
  • Both genders
  • Diagnosed with Text Neck Syndrome by a forward head posture with craniovertebral angle less than 50 degrees
  • Neck pain with a Visual Analog Scale (VAS) score of 3 or higher out of 10
  • Neck pain intensity with a Neck Disability Index (NDI) score greater than 10%
  • Perceived Stress Scale-10 (PSS-10) score over 14 with daily gadget use and forward head posture
  • Use of handheld digital devices like smartphones or tablets for 3 or more hours daily
Not Eligible

You will not qualify if you...

  • History of cervical trauma, surgery, or congenital spine deformity
  • Diagnosed cervical disorders such as spondylosis, spondylolisthesis, or disc herniation
  • Any neurological condition affecting cognition or previous cervical spine surgery
  • History of diagnosed anxiety or psychiatric conditions
  • Currently receiving physical therapy or using muscle relaxants or painkillers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Zara Zahid

Lahore, Punjab Province, Pakistan, 54600

Actively Recruiting

2

Dr. Wajeeha Mahmood

Lahore, Pakistan

Actively Recruiting

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Research Team

Z

Zara Zahid, Doctor of Physical Therapy

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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