- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07720492
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
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
Study Overview
Status
Conditions
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).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab Province
-
Faisalabad, Punjab Province, Pakistan, 38000
- The University of Faisalabad (TUF)
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
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:
- Recent cervical spine fracture/injury
- Congenital malformation
- Recent history of head and neck surgery
- Congenital torticollis
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
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.
|
A moist hot pack was applied to the cervical region for 10 minutes before the manual therapy intervention in both study groups
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
|
|
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
|
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
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Craniovertebral Angle
Time Frame: Baseline and Week 12 (end of the intervention)
|
Craniovertebral angle was measured using a universal goniometer to assess forward head posture
|
Baseline and Week 12 (end of the intervention)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain intensity
Time Frame: Baseline and Week 12 (end of intervention)
|
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)
|
Baseline and Week 12 (end of intervention)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Noreen Kiran, PhD, University of Faisalabad
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2023-MS-PT-064
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Forward Head Posture
-
Sahmyook UniversityCompletedForward Head Posture | Normal Head PostureSouth Korea
-
Cairo UniversityRecruiting
-
Riphah International UniversityRecruitingForward Head PosturePakistan
-
Beirut Arab UniversityRecruitingForward Head PostureLebanon
-
Egyptian Chinese UniversityRecruitingForward Head PostureEgypt
-
Cairo UniversityNot yet recruiting
-
Cairo UniversityRecruitingForward Head PostureEgypt
-
Dokuz Eylul UniversityThe Scientific and Technological Research Council of TurkeyCompletedForward Head PostureTurkey (Türkiye)
-
Tokat Gaziosmanpasa UniversityCompleted
-
Cukurova UniversityCompletedForward Head PostureTurkey
Clinical Trials on Moist Heat Therapy
-
King Saud UniversityCompletedTendinopathy | LasersSaudi Arabia
-
Alexandria UniversityCompletedPain, Postoperative | Wound HealEgypt
-
University of HailCompleted
-
Universidad Católica del MauleCompletedPhysical Therapy Techniques
-
University of DelawareCompletedLow Back PainUnited States
-
University of Alabama at BirminghamBruder Healthcare CompanyCompletedMeibomian Gland Dysfunction | Dry Eye Disease | Contact Lens DiscomfortUnited States
-
Dow University of Health SciencesCompletedForward Head Posture | Upper Cross SyndromePakistan
-
Foundation University IslamabadCompletedLow Back Pain | Sciatica | Low Back Pain, MechanicalPakistan
-
Integra LifeSciences CorporationTerminatedFoot Ulcer, DiabeticUnited States, Puerto Rico
-
Tribhuvan University, NepalCompletedLabour Pain | Heat Therapy | Cold TherapyNepal