Comparative Effects of SNAG Vis GONG's Mobilization in Text Neck Syndrome Patients
SNAG-GONG
Comparative Effects of SNAG Versus GONG's Mobilization in Text Neck Syndrome Among Final Year Medical Students of The University of Faisalabad
1 other identifier
interventional
48
1 country
1
Brief Summary
Text neck syndrome is a common musculoskeletal disorder caused by prolonged smartphone and computer use, resulting in neck pain, forward head posture, and functional disability. Manual therapy techniques, including Sustained Natural Apophyseal Glides (SNAG) and GONG's Mobilization, are frequently used to manage cervical dysfunction. This quasi-experimental pretest-posttest comparative study aimed to compare the effectiveness of SNAG and GONG's Mobilization on pain intensity, craniovertebral angle, and neck disability in individuals with text neck syndrome. Participants divided into 2 groups (Treatment group A and B) were undergo baseline and post-intervention assessments followed a 12-week treatment program
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
1 active site
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
October 25, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 10, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 15, 2026
CompletedFirst Submitted
Initial submission to the registry
July 17, 2026
CompletedFirst Posted
Study publicly available on registry
July 22, 2026
CompletedJuly 22, 2026
July 1, 2026
6 months
July 17, 2026
July 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Craniovertebral Angle
Craniovertebral angle was measured using a universal goniometer to assess forward head posture
Baseline and Week 12 (end of the intervention)
Secondary Outcomes (1)
Pain intensity
Baseline and Week 12 (end of intervention)
Study Arms (2)
Baseline PLUS GONG's mobilization
EXPERIMENTALParticipants in this arm received baseline treatment consisting of a moist hot pack applied to the cervical region for 10 minutes, followed by GONG's Mobilization. GONG's Mobilization was administered for 10-15 repetitions per session over approximately 20 minutes, three sessions per week on alternate days for 12 weeks. Outcome measures, including pain intensity (Numeric Pain Rating Scale), craniovertebral angle, and Neck Disability Index, were assessed before and after the intervention period.
Baseline plus SNAG
ACTIVE COMPARATORParticipants in this arm received baseline treatment consisting of a moist hot pack applied to the cervical region for 10 minutes, followed by Sustained Natural Apophyseal Glides (SNAG). SNAG was administered for 10-15 repetitions per session over approximately 20 minutes, three sessions per week on alternate days for 12 weeks. Outcome measures, including pain intensity (Numeric Pain Rating Scale), craniovertebral angle, and Neck Disability Index, were assessed before and after the intervention period
Interventions
GONG's Mobilization was administered to the cervical spine using 10-15 repetitions per session for approximately 20 minutes, three sessions per week on alternate days for 12 weeks
A moist hot pack was applied to the cervical region for 10 minutes before the manual therapy intervention in both study groups
SNAG mobilization was applied to the cervical spine with 10-15 repetitions per session for approximately 20 minutes, 3 sessions per week on alternate days for 12 weeks
Eligibility Criteria
You may qualify if:
- Both Male and Female who engage in prolonged computer and phone usage for more than 4 hours per day for over a year
- Neck pain (3 to 8 on NPRS)
- Altered cranio-vertebral angle\<49 degree
You may not qualify if:
- Recent cervical spine fracture/injury
- Congenital malformation
- Recent history of head and neck surgery
- Congenital torticollis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The University of Faisalabad (TUF)
Faisalabad, Punjab Province, 38000, Pakistan
Study Officials
- PRINCIPAL INVESTIGATOR
Noreen Kiran, PhD
University of Faisalabad
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr Noreen Kiran; PT
Study Record Dates
First Submitted
July 17, 2026
First Posted
July 22, 2026
Study Start
October 25, 2025
Primary Completion
April 10, 2026
Study Completion
June 15, 2026
Last Updated
July 22, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share