Comparing two techniques for treating mechanical neck pain
Comparison of Cervical Sustained Natural Apophyseal Glide and Instrument Assisted Soft Tissue Mobilization on Mechanical Neck Pain
This study is testing two different treatments for neck pain to see which one helps people aged 20 to 45 feel better and move their necks more easily.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 56 (estimated) |
| Ages | 20 Years to 45 Years |
| Sex | All |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Rawalpindi, Punjab Province) |
| Trial ID | NCT06598644 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of two therapeutic techniques, Cervical Sustained Natural Apophyseal Glide (SNAG) and Instrument-Assisted Soft Tissue Mobilization (IASTM), in treating mechanical neck pain. Participants will receive either SNAG or IASTM combined with conventional physical therapy to assess pain reduction, range of motion improvement, and overall neck function enhancement. The study targets individuals aged 20 to 45 with a history of neck pain lasting more than three months, focusing on specific muscle tenderness and pain during head movements.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 20 to 45 with chronic neck pain lasting over three months and specific tenderness in neck muscles.
Not a fit: Patients with recent neck injuries, surgeries, or specific conditions like radiculopathy or rheumatoid arthritis may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide patients with more effective treatment options for managing mechanical neck pain.
How similar studies have performed: Previous studies have shown promise in using similar manual therapy techniques for neck pain, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * • Both genders (males and females) * Age between 20 and 45 years * History of neck pain \>3 month, with tenderness on palpation present on sternocleidomastoid and Levator scapulae muscles and pain aggravated by activities involving turning head towards the side * Patients with pain on NPRS (at least 3) Exclusion Criteria: * • patients with recent injuries or surgeries in and around the neck region * Cervical nerve root lesion (radiculopathy) * Traumatic injuries like whiplash injury * malignancy in and around the neck region * rheumatoid arthritis * pregnant females * cervicogenic headache * Patients with unwillingness or inability to provide informed consent * Current participation in another neck pain treatment program
Where this trial is running
Rawalpindi, Punjab Province
- Pakistan Railway hospital — Rawalpindi, Punjab Province, Pakistan (Recruiting)
Study contacts
- Principal investigator: Kinza Anwar, Ms-Ompt — Riphah International University
- Study coordinator: Kinza Anwar, Ms-Ompt
- Email: kinza.anwar@riphah.edu.pk
- Phone: +92-3239735427
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.