Actively Recruiting
Effects of SNAGs & CBT on Pain, Craniovertebral Angle & Disability in Non Specific Neck Pain
Led by Riphah International University · Updated on 2025-07-04
32
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Non-specific neck pain is a prevalent condition causing discomfort, reduced craniovertebral angle, and disability. This randomized controlled trial will evaluate the combined effects of Sustained Natural Apophyseal Glides (SNAGs) and Cognitive Behavioral Therapy (CBT) on pain, posture, and function. Group A will receive SNAGs and CBT, while Group B will undergo SNAGs with cervical stabilization exercises, twice weekly for four weeks. Outcomes will include pain, craniovertebral angle, and disability, analyzed using SPSS.
CONDITIONS
Official Title
Effects of SNAGs & CBT on Pain, Craniovertebral Angle & Disability in Non Specific Neck Pain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 to 28 years
- Male or female participants
- Craniovertebral angle less than 53 degrees
- Grade 2 neck pain according to KNGF Guidelines
- Localized pain or stiffness between C3 and C7 vertebrae without upper limb radiculopathy
- No neck pain treatment received in the last 3 months
- Willingness to sign a written consent form
You will not qualify if you...
- History of spinal surgery
- Neck pain caused by rheumatoid arthritis, ankylosing spondylitis, fracture, tumor, or similar conditions
- Nerve root compression
- Positive vertebrobasilar artery test
- Severe radiculopathy
- Osteoporosis or osteopenia
- Long-term use of corticosteroids or anticoagulants
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Syeda Khatoon e Jannat Trust Hospital,
Faisalabad, Punjab Province, Pakistan, 38000
Actively Recruiting
Research Team
I
Imran Amjad, pHD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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