Neck Pain Clinical Trial
Official title:
The Comparative Effectiveness of Mechanical Diagnosis and Therapy and Management According to the Cervical Spine Clinical Practice Guidelines in People With Neck Pain Who Exhibit Directional Preference: A Randomized Clinical Trial
The goal of this clinical trial is to compare physical therapy treatments in people with neck pain. The main aim is to compare the short-term effectiveness of physical therapy treatment for neck pain as delivered through Mechanical Diagnosis and Therapy (MDT) as compared to the Cervical Spine Clinical Practice Guidelines (CPGs) in patients with neck pain. Participants will be randomly allocated to receive treatment according to MDT or CPG guidelines. Researchers will compare outcomes between the two groups over 1 year.
| Status | Not yet recruiting |
| Enrollment | 200 |
| Est. completion date | July 1, 2025 |
| Est. primary completion date | January 1, 2025 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 90 Years |
| Eligibility | Inclusion Criteria: 1. Patients who are consecutively referred to physical therapy for the treatment of neck pain will be recruited from three hospital-based outpatient physical therapy clinics. Patients will be included if they demonstrate directional preference in the physical therapy initial examination. 2. Patients aged 18-90 years Exclusion Criteria: Patients will be excluded if they: 1. Have a history of spinal surgery 2. Have cervical instability, and/or vertebral basilar insufficiency 3. Have a serious medical condition such as cancer, spondylolisthesis, rheumatoid arthritis, ankylosing spondylitis, or other related autoimmune diseases 4. Are currently pregnant 5. Are positive for upper motor neuron signs 6. Are experiencing problems with dizziness, tinnitus, swallowing, or bowel and bladder dysfunction. 7. Do not experience directional preference in the physical therapy initial examination. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Shirley Ryan AbilityLab | Chicago | Illinois |
| United States | Good Shepard Penn Partners | Radnor | Pennsylvania |
| United States | WellSpan Health | York | Pennsylvania |
| Lead Sponsor | Collaborator |
|---|---|
| Tufts University |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Neck Disability Index (NDI) | The NDI is an outcome tool used to measure patient's perceived level of function in relation to their neck pain. | 1 year | |
| Secondary | Fear Avoidance Belief Questionnaire (FABQ) | The FABQ is an outcome tool used to measure a patient's fear in relation to their neck pain. | 1 year | |
| Secondary | Numerical Pain Rating Scale (NPRS) | The NPRS is a tool used to measure the patient's perception of the neck pain on a scale ranging from 0-10 with 10 representing the worst pain possible. | 1 year | |
| Secondary | Patient Specific Functional Scale (PSFS) | The PSFS is an outcome tool used to assess which particular functional activities are most impacted by their pain. | 1 year | |
| Secondary | Global Rating of Change Scale (GROC) | The GROC is an outcome tool used independently to measure improvements in a patient's condition or as an anchor for other outcome measures. | 1 year |
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