Comparing Physical Therapy Interventions on Craniovertebral Angle (CVA) in Cervical Myofas
Myofascial pain syndrome (MPS) and radiculopathy are prevalent musculoskeletal conditions that afflict a substantial portion of the population, causing significant discomfort and impairments in daily functioning. MPS is characterized by localized muscle pain, trigger points, and referred pain, often accompanied by stif
| Condition(s) | Myofascial Pain Syndrome - Neck |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | Myofascial pain syndrome (MPS) and radiculopathy are prevalent musculoskeletal conditions that afflict a substantial portion of the population, causing significant discomfort and impairments in daily functioning. MPS is characterized by localized muscle pain, trigger points, and referred pain, often accompanied by stiffness and restricted range of motion. A common feature shared by individuals with MPS and radiculopathy is the presence of postural abnormalities and balance impairments . The craniovertebral angle, which reflects the relationship between the head and neck, is often compromised in these individuals due to muscle imbalances, pain-related guarding, and structural changes in the spine. Various physiotherapy modalities, including dry needling, manual mobilization and soft tissue |
| Who can participate | Inclusion Criteria: 1. Age: Participants must be between 20 and 40 years old. 2. Gender: Both genders, Male and Female have equal chance of selection as participant in the study. 3. Diagnosis: Participants must have a confirmed diagnosis of myofascial pain syndrome (MPS), altered cervical posture, restricted range of motion of cervical spine due to muscular spasm etc, altered craniovertebral angle, pain in cervical region or upper extremity and/or radiculopathy by a qualified healthcare professional, based on standardized diagnostic criteria (e.g., clinical examination, imaging studies). 4. Severity: Participants should have mild to moderate symptoms of MPS and/or radiculopathy, as determined by the assessing healthcare provider. 5. Willingness to Participate: Participants must be willing |
| Ages | 20 Years to 40 Years |
| Sex | All |
| Lead sponsor | National Orthopedic and General Hospital |
| Locations | Bahawalpur, Punjab Province, Pakistan |
| Start date | 2025-03-15 |
| NCT ID | NCT07098754 |
| Official listing | https://clinicaltrials.gov/study/NCT07098754 |