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CompletedNCT07720492SNAG-GONGUpdated Jul 22, 2026

Comparative Effects of SNAG Vis GONG's Mobilization in Text Neck Syndrome Patients

An interventional study of Moist Heat Therapy and Sustained Natural Apophyseal Glide (SNAG) in Text Neck Syndrome and Forward Head Posture, sponsored by University of Faisalabad. Completed at 1 site in Pakistan. Open to participants aged 18 Years to 25 Years. Per ClinicalTrials.gov, last updated 2026-07-22.

Sponsored by University of Faisalabad · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Oct 2025, registered Jul 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
48
Allocation
Non-randomized
Ages
18 Years to 25 Years
Sex
All
01

Study 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

Read the detailed description

Text neck syndrome has emerged as a growing health concern due to increased use of smartphones, laptops, and other digital devices. Prolonged forward head posture places excessive mechanical stress on cervical structures, leading to neck pain, muscle imbalance, postural abnormalities, and functional limitations.

Manual therapy interventions such as Sustained Natural Apophyseal Glides (SNAG) and GONG's Mobilization have demonstrated beneficial effects in managing cervical spine dysfunction. However, evidence comparing these two techniques specifically in individuals with text neck syndrome remains limited.

A quasi-experimental pretest-posttest comparative study conducted. 48 participants were recruited aged 18-25 years from The University of Faisalabad. Participants diagnosed with text neck syndrome allocated into two treatment groups according to the study protocol. The participants divided into 2 groups (A and B) Both groups received moist heat therapy for 10 minutes before intervention. Group A received SNAG mobilization, while Group B received GONG's Mobilization. Treatment sessions were conducted three times per week on alternate days for 12 weeks.

Outcomes and outcome measuring tools were pain intensity by using the Numeric Pain Rating Scale (NPRS), Craniovertebral angle by Goniometer, and neck disability by Neck Disability Index (NDI).

02

Conditions studied

  • Text Neck Syndrome
  • Forward Head Posture

Keywords

  • Text neck syndrome
  • Forward head posture
  • GONG's Mobilization
  • sustained natural appophyseal glide
  • neck disability
  • craniovertebral angle
03

In context

Lead sponsor

University of Faisalabad is the lead sponsor of 83 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 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

Exclusion criteria

Exclusion Criteria:

  • Recent cervical spine fracture/injury
  • Congenital malformation
  • Recent history of head and neck surgery
  • Congenital torticollis
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
48 participants (actual)

Study arms

  • Experimental
    Baseline PLUS GONG's mobilization

    Participants 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.

    Procedure: Moist Heat Therapy · Procedure: GONG's Mobilization

  • Active comparator
    Baseline plus SNAG

    Participants 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

    Procedure: Moist Heat Therapy · Procedure: Sustained Natural Apophyseal Glide (SNAG)

Interventions

  • ProcedureMoist Heat Therapy

    A moist hot pack was applied to the cervical region for 10 minutes before the manual therapy intervention in both study groups

  • ProcedureSustained Natural Apophyseal Glide (SNAG)

    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

  • ProcedureGONG's Mobilization

    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

06

What researchers measure

Primary outcomes

  1. Craniovertebral Angle

    Craniovertebral angle was measured using a universal goniometer to assess forward head posture

    Time frame: Baseline and Week 12 (end of the intervention)

Secondary outcomes

  1. Pain intensity

    Pain intensity was assessed using the Numeric Pain Rating Scale (NPRS), an 11-point self-reported scale ranging from 0 (no pain) to 10 (worst imaginable pain)

    Time frame: Baseline and Week 12 (end of intervention)

07

Study locations

1 site
  • The University of Faisalabad (TUF)
    Faisalabad, Punjab Province 38000, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07720492
Lead sponsor
University of Faisalabad
Responsible party
Dr Noreen Kiran; PT (Dr Noreen Kiran; PT, University of Faisalabad) — Principal investigator
First posted
Jul 22, 2026
Start date
Oct 25, 2025
Primary completion
Apr 10, 2026
Completion
Jun 15, 2026
Last update
Jul 22, 2026

Study contacts

Noreen Kiran, PhD
principal investigator · University of Faisalabad

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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