Effect of Myofascial Release Therapy on University Students With Text Neck Syndrome.
1 other identifier
interventional
62
1 country
2
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 22, 2026
CompletedFirst Submitted
Initial submission to the registry
February 24, 2026
CompletedFirst Posted
Study publicly available on registry
March 2, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 22, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 5, 2026
CompletedMarch 2, 2026
February 1, 2026
28 days
February 24, 2026
February 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Neck Pain
Neck pain will be assessed using the Visual Analog Scale (VAS), where participants rate their pain intensity on a scale from 0 (no pain) to 10 (worst imaginable pain)
Baseline and after 4 weeks of intervention
Perceived Stress
Perceived stress will be assessed using the Perceived Stress Scale (PSS), a validated questionnaire measuring the degree to which situations in one's life are appraised as stressful.
Baseline and after 4 weeks of intervention
Forward Head Posture
Forward Head Posture will be measured using the craniovertebral angle (CVA) from lateral photographs using Kinovea Software. A smaller angle indicates a more pronounced forward head posture.
Baseline and after 4 weeks
Study Arms (2)
Intervention
EXPERIMENTALParticipants will receive Myofascial Release Therapy targeting neck and upper back which will release the fascial restrictions by providing sustained pressure. Outcomes such as neck pain, forward head posture, and perceived stress will be measured after the intervention.
Conventional Physical Therapy
ACTIVE COMPARATORParticipants will receive conventional physiotherapy including postural correction exercises, stretching of neck and upper back muscles, and ergonomic education. Outcomes will be measured after the intervention.
Interventions
Participants will receive Myofascial Release Therapy targeting neck and upper back muscles, 3 sessions per week for 4 weeks. This is a physical therapy intervention.
Participants will receive conventional physiotherapy including postural correction exercises, stretching of neck and upper back muscles, and ergonomic education. Outcomes will be measured after the intervention.
Eligibility Criteria
You may qualify if:
- \. university students from age group of 18-30 2. Both genders 3. Students with Text Neck Syndrome diagnosed via Forward head Posture (through measuring craniovertebral angle) \<50° 4. Minimum Pain measured by Visual Analog Scale (VAS) ≥ 3/10 5. Pain Intensity measured through Neck Disability Index (NDI \> 10%) 6. A PSS-10 Score of \>14 in individuals with daily gadget use and FHP. 7. Usage of handheld digital gadgets including smartphones and tablets ≥ 3 hours
You may not qualify if:
- \. History of cervical trauma, surgery or any spine deformity which is congenital 2. History of diagnosed cervical disorders i.e cervical spondylosis, cervical spondylolisthesis, disc herniation 3. Any diagnosed neurological condition which affects cognition or any previous cervical spine surgery 4. Any history of diagnosed anxiety and psychiatric conditions 5. Currently receiving any form of physical therapy or using any muscle relaxants or painkillers
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Zara Zahid
Lahore, Punjab Province, 54600, Pakistan
Dr. Wajeeha Mahmood
Lahore, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Zara Zahid, Doctor of Physical Therapy
University of Health Sciences Lahore
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- This will be an assessor blinded Randomized Controlled Trial. Outcome assessors measuring neck pain, forward head posture, and perceived stress will be blinded to group assignment. Participants and therapists are not blinded due to the nature of the intervention
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr. Zara Zahid
Study Record Dates
First Submitted
February 24, 2026
First Posted
March 2, 2026
Study Start
February 22, 2026
Primary Completion
March 22, 2026
Study Completion
April 5, 2026
Last Updated
March 2, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared.