NCT07444112

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
62

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

2 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 22, 2026

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

February 24, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 2, 2026

Completed
20 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 22, 2026

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 5, 2026

Completed
Last Updated

March 2, 2026

Status Verified

February 1, 2026

Enrollment Period

28 days

First QC Date

February 24, 2026

Last Update Submit

February 24, 2026

Conditions

Keywords

text neck syndromeneck painforward head postureperceived stressmyofascial release therapyrandomized controlled trial

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

EXPERIMENTAL

Participants 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.

Behavioral: Myofascial Release TherapyBehavioral: Standard Care (Treatment as Usual)

Conventional Physical Therapy

ACTIVE COMPARATOR

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.

Behavioral: Standard Care (Treatment as Usual)

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.

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.

Conventional Physical TherapyIntervention

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

RECRUITING

Dr. Wajeeha Mahmood

Lahore, Pakistan

RECRUITING

MeSH Terms

Conditions

Neck Pain

Interventions

Myofascial Release TherapyStandard of CareTherapeutics

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

MassageTherapy, Soft TissueMusculoskeletal ManipulationsComplementary TherapiesPhysical Therapy ModalitiesRehabilitationQuality Indicators, Health CareQuality of Health CareHealth Services AdministrationHealth Care Quality, Access, and Evaluation

Study Officials

  • Zara Zahid, Doctor of Physical Therapy

    University of Health Sciences Lahore

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Zara Zahid, Doctor of Physical Therapy

CONTACT

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
Model Details: Participants are randomly assigned to either Myofascial Release Therapy group or conventional physiotherapy group, and outcomes will be measured at baseline and after the intervention period.
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.

Locations