Health Condition 1: M999- Biomechanical lesion, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Acute mechanical neck pain group Adults (greater than 18 years) Both men and women Acute mechanical neck pain (less than 6 weeks) Chronic mechanical neck pain group Adults (greater than 18 years) Both men and women Chronic mechanical neck pain (greater than 12 weeks)
Exclusion criteria
Exclusion criteria: Diagnosis of fibromyalgia whiplash-associated injury or trauma Cervical spine surgery Clinical diagnosis of cervical radiculopathy or myelopathy or cervical disc herniation Malignancy or systemic inflammatory conditions Shoulder related conditions (rotator cuff tendinopathy, shoulder impingement) Any active injuries or skin infection in the lower leg
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of this cross-sectional study is to compare pressure pain threshold in individuals with acute and chronic mechanical neck pain.Timepoint: The data will be collected at a single time point from individuals with mechanical neck pain using Quantitative Sensory Testing (QST). Each participant will undergo a testing session lasting approximately 15-20 minutes. No follow-up sessions are planned, as the study is cross-sectional and exploratory in nature. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome of this study is to compare two-point discrimination & temporal summation in individuals with acute & chronic mechanical neck pain. Also to explore associations between quantitative sensory test outcomes, pain intensity (numerical pain rating scale) & neck pain duration.Timepoint: The secondary outcome is assessed only once at the first OPD visit (baseline) | — |
Countries
India
Contacts
Manipal College of Health Professions