Neck Pain Clinical Trial
Official title:
Pain Modulatory Profiles in Massage for Individuals With Neck Pain
NCT number | NCT03534739 |
Other study ID # | IRB201800840 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 20, 2018 |
Est. completion date | June 9, 2022 |
Verified date | July 2022 |
Source | University of Florida |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
One in ten adults experience widespread pain. Neck pain, for example, is a prevalent condition with a high rate of recurrence that affects between 10.4% and 21.3% of the population annually. Massage is a common manual therapy intervention for individuals with musculoskeletal pain. However, the mechanisms of massage are not well established. Also, the conditioned pain modulation (CPM) paradigm is a dynamic quantitative sensory testing measure of a pain inhibitory process in which pain sensitivity is lessened in response to a remotely applied painful stimulus. This study will evaluate the association between pain inducing massage and the conditioned pain modulation paradigm in participants with a history of neck pain.
Status | Completed |
Enrollment | 26 |
Est. completion date | June 9, 2022 |
Est. primary completion date | June 9, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - currently experiencing neck pain with or without arm pain - neck pain symptom intensity rated as 4/10 or higher during the last 24 hours - neck pain for greater than or equal to 3 months Exclusion Criteria: - non-English speaking - systemic medical conditions known to affect sensation (e.g. diabetes, hypertension) - history of neck surgery or fracture within the past 6 months - current history of chronic pain condition other than neck pain - diagnosis of cervical radiculopathy or cervical myelopathy - history of whiplash; g) currently using blood thinning medication - any blood clotting disorder such as hemophilia - any contraindication to application of ice, such as: uncontrolled hypertension, cold urticaria, cryoglobulinemia, paroxysmal cold hemoglobinuria, and circulatory compromise. |
Country | Name | City | State |
---|---|---|---|
United States | UF Health | Gainesville | Florida |
Lead Sponsor | Collaborator |
---|---|
University of Florida |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline in Pressure Pain Threshold | Pressure in kilograms at which ascending pressure stimulus first changes from pressure to painful | 2 hours | |
Secondary | Change from baseline in Thermal Pain Threshold and Tolerance | Temperature at which ascending thermal stimulus first changes from warm to painful and maximum temperature tolerated | 2 hours | |
Secondary | Change from baseline in Pressure Pain Tolerance | Pressure in kilograms at which ascending pressure is no longer tolerated | 2 hours | |
Secondary | Change from baseline in Ramp and Hold | Participants will rate their pain using a 101 point mechanical visual analog scale to thermal stimuli of 45, 47, 49, and 50 degree Celsius each of 5 seconds duration will be applied to the forearm and to the muscle on the side of the neck | 2 hours | |
Secondary | Change from baseline in Temporal Summation | Participants will rate their pain using a 0 to 10 numeric rating scale to a train of 10 50 degree Celsius heat pulses will be applied to the skin in the plantar surface of the hand. | 2 hours | |
Secondary | Change from baseline in Conditioned Pain Modulation | Pressure in kilograms at which ascending pressure stimulus applied to the foot first changes from pressure to painful both prior to and immediately following immersion of the opposite hand in a cold water bath | 2 hours |
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