Neck Pain Clinical Trial
Official title:
Dry-needling Added to Physical Therapy for Treating Patients With Chronic Non-specific Neck Pain: a Randomized Controlled Trial
NCT number | NCT02927977 |
Other study ID # | DRY01 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | December 2016 |
Est. completion date | March 2018 |
Verified date | November 2018 |
Source | Federal University of Health Science of Porto Alegre |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this randomized clinical trial is to verify the effectiveness of the addition of the dry needling in individuals with non-specific neck pain who receive a multimodal physical therapy rehabilitation program.
Status | Completed |
Enrollment | 116 |
Est. completion date | March 2018 |
Est. primary completion date | May 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - able to speaking and reading in Portuguese, severity of the symptoms at least 3 points on 0-10 numeric pain rating and at least 14% disability on Neck Disability Index. Exclusion Criteria: - history of whiplash associated injuries, fibromyalgia, cervical spine symptoms of radiculopathy or myelopathy, use of anticoagulant medication, pregnancy, history of spinal surgeries and "red flags" (spinal fracture, inflammatory diseases, tumor, fracture, rheumatoid arthritis, osteoporosis). |
Country | Name | City | State |
---|---|---|---|
Brazil | UFCSPA | Porto Alegre | RS |
Lead Sponsor | Collaborator |
---|---|
Federal University of Health Science of Porto Alegre |
Brazil,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | pain intensity | measured by 11-point numeric rating scale | 4 weeks after randomisation | |
Primary | disability | measured by neck disability index | 4 weeks after randomisation | |
Secondary | pain intensity | measured by 11-point numeric rating scale | 12, 24 weeks after randomisation | |
Secondary | disability | measured by neck disability index | 12, 24 weeks after randomisation | |
Secondary | global perceived effect | measured by global perceived rating scale | 4,12, 24 weeks after randomisation | |
Secondary | quality of sleep | measure by Pittsburgh quality index | 4,12, 24 weeks after randomisation | |
Secondary | catastrophizing | measure by pain catastrophizing scale | 4,12, 24 weeks after randomisation | |
Secondary | self-efficacy | measured by The Pain Self-Efficacy Questionnaire | 4,12, 24 weeks after randomisation | |
Secondary | adverse events | record of the adverse events | 24h, 72h and four weeks after randomisation |
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