Neck Pain Clinical Trial
Official title:
Immediate and Short-term Effect of Biofreeze® Versus Placebo on Acute Neck Pain, Disability, and Range of Motion
Verified date | October 2019 |
Source | Sport and Spine Rehab Clinical Research Foundation |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study to compare the effect of Biofreeze® versus a Placebo on neck pain, disability, fear avoidance, and range of motion prior to and following cervical manipulation over the course of one week among patients with acute neck pain.
Status | Completed |
Enrollment | 59 |
Est. completion date | February 1, 2019 |
Est. primary completion date | December 1, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - neck pain for less than 2 weeks and >18 years of age Exclusion Criteria: - pregnancy, cancer, or a corticosteroid injection within the past 2 weeks. Additionally, anyone who has a history of neck surgery will be excluded |
Country | Name | City | State |
---|---|---|---|
United States | Sport and Spine Rehab | Landover | Maryland |
Lead Sponsor | Collaborator |
---|---|
Sport and Spine Rehab Clinical Research Foundation |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Numeric Pain Rating Scale (NPRS) at 1 week | Baseline (T1), 10 minutes after application (T2), immediately following manipulation [15 minutes after application] (T3), 1 week (T4) | ||
Primary | Change in Neck Disability Index (NDI) at 1 week | Baseline (T1), 1 week (T4) | ||
Primary | Change Cervical Range of Motion at 1 week | Using FDA cleared DorsaVi sensor system to measure cervical flexion, extension, side bending, and rotation | Baseline (T1), 1 week (T4) |
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