NCT07720492

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

87
On Track

Trial Health Score

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

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

October 25, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 10, 2026

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

July 17, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 22, 2026

Completed
Last Updated

July 22, 2026

Status Verified

July 1, 2026

Enrollment Period

6 months

First QC Date

July 17, 2026

Last Update Submit

July 17, 2026

Conditions

Keywords

Text neck syndromeForward head postureGONG's Mobilizationsustained natural appophyseal glideneck disabilitycraniovertebral angle

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

EXPERIMENTAL

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 TherapyProcedure: GONG's Mobilization

Baseline plus SNAG

ACTIVE COMPARATOR

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 TherapyProcedure: Sustained Natural Apophyseal Glide (SNAG)

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

Baseline PLUS GONG's mobilization

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

Baseline PLUS GONG's mobilizationBaseline plus 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

Baseline plus SNAG

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Location

Study Officials

  • Noreen Kiran, PhD

    University of Faisalabad

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: The study was conducted with a nonrandomized, pretest-posttest quasi-experimental design of 2 parallel groups. As per the study protocol, the participants were randomly allocated to one of the two intervention groups. Pre and after intervention assessments were done to examine the effects of SNAG and GONG's Mobilization on pain, craniovertebral angle and neck impairment after a 12 week treatment period.
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

Locations