- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07387016
Self-Mobilization With SNAGs Vs. DIE on CMNP in Computer Professionals
Self-Mobilization With Self-Applied Sustained Natural Apophyseal Glides Versus Dynamic Isometric Exercises for Chronic Mechanical Neck Pain in Computer Professionals: A Randomized Controlled Trial
The goal of this clinical trial was to find out whether a self-applied neck mobilization technique (called self-SNAGs) or neck strengthening exercises (dynamic isometric exercises) works better to reduce pain and improve daily function in computer professionals aged 25-45 years who had long-lasting mechanical neck pain.
The main questions it aimed to answer were:
- Does self-SNAG treatment reduce neck pain more than strengthening exercises?
- Does self-SNAG treatment improve neck-related daily activities more than strengthening exercises?
Researchers compared self-SNAG exercises with dynamic isometric neck exercises to see which approach led to greater pain relief and better function over six weeks.
Participants were asked to:
- Perform either self-SNAG neck movements using a towel or neck-strengthening exercises using elastic bands.
- Do the exercises five days per week for six weeks.
- Follow ergonomic advice for proper posture during computer work.
- Complete pain and disability questionnaires before and after the program.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Utter Pradesh
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Greater Noida, Utter Pradesh, India, 201315
- Prakash Institute of Physiotherapy Rehabililation and Allied Medical Sciences
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Participants' ages ranged from 25 to 45 years.
- Having chronic mechanical neck pain persisting for at least 3 months.
- Computer users of at least 4 to 5 hours daily for greater than 3 years.
- Understand and be able to perform the indicated exercises well.
- Cooperation in the study with voluntary participation.
Exclusion Criteria:
- Prior history of musculoskeletal neck disorders, trauma, fracture, inflammation, malignancy, active infection, any neurological disorders or deficits, and any spinal surgeries.
- Acute mechanical neck pain
- Non-cooperation in the study,
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Self-SNAGs Group
Participants assigned to the self-SNAG arm engaged in structured Mulligan self-mobilization sessions conducted on a five-day weekly schedule for six weeks, with ongoing oversight and instructional feedback to promote correct application and consistent participation.
|
Participants in the Self-SNAG Group performed self-administered cervical SNAG mobilizations using a towel following initial physiotherapist instruction to ensure correct technique.
Movements included cervical extension, bilateral rotation, and bilateral lateral flexion.
The towel edge was placed beneath the targeted vertebral level to apply a sustained glide while participants actively moved through the available range, with brief end-range overpressure before returning to neutral.
Each movement was repeated 6-10 times per session.
Other Names:
All participants of both groups received a standard ergonomic education and postural advice program, which included guidance on neutral spine alignment, workstation optimization, and the incorporation of regular movement breaks during computer work to minimize cervical strain.
|
|
Active Comparator: DIE Group
Participants assigned to the DIE arm performed structured dynamic isometric cervical exercises using elastic resistance bands.
Sessions were conducted on a five-day weekly schedule for six weeks, with ongoing oversight and instructional feedback to promote correct application and consistent participation.
|
All participants of both groups received a standard ergonomic education and postural advice program, which included guidance on neutral spine alignment, workstation optimization, and the incorporation of regular movement breaks during computer work to minimize cervical strain.
Participants in the DIE Group performed dynamic isometric exercises using elastic resistance bands, including resisted flexion, extension, and lateral flexion.
The band was secured around the head and anchored to a stable surface while participants maintained upright posture and controlled cervical alignment.
The head was displaced approximately 10 cm against resistance and slowly returned to the starting position.
Each session comprised 2-3 sets of 10-15 repetitions per movement, with instruction to prevent compensatory motions.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Intensity
Time Frame: 6 weeks
|
Pain intensity was assessed using a reliable and valid Visual Analog Scale, marked with 0 and 10 at either end, indicating no pain and unbearable pain, respectively.
|
6 weeks
|
|
Functional Disability
Time Frame: 6 weeks
|
Participants' functional disability was measured using the reliable and validated Neck Disability Index (NDI), with total scores ranging from 0 (no disability) to 50 (severe disability).
|
6 weeks
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Ahmad H. Alghadir, PhD, King Saud University
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
- RRC-2021-03
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.
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