Analgesia Clinical Trial
Official title:
Effect of Exercise on Pain Responses in Non-Hispanic Blacks and Whites
NCT number | NCT03609957 |
Other study ID # | R01HL141205 |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | |
Last updated | |
Start date | February 2019 |
Est. completion date | December 2019 |
Verified date | December 2018 |
Source | Georgia State University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Non-Hispanic Blacks tend to report higher levels of pain, experience pain more frequently, and be under-treated for pain compared to non-Hispanic Whites. Acute (single session) exercise is known to be effective at reducing pain but it is unknown what effect chronic exercise training has on pain responses. The broad goal of this study is to determine whether regular exercise training is more effective at reducing pain responses in non-Hispanic Blacks compared to non-Hispanic Whites. The investigators are interested in comparing regular aerobic exercise training versus high-intensity interval training.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 2019 |
Est. primary completion date | December 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 40 Years |
Eligibility |
Inclusion Criteria: - Healthy - Normotensive - Identify as non-Hispanic Black or non-Hispanic White - Healthy enough to participate in regular exercise - Not taking any medications other than birth control Exclusion Criteria: - Heart disease (high blood pressure, previous stroke or heart attack) - Type 1 or 2 diabetes - History of cancer treated with chemotherapy - History of nerve damage - History of chronic pain - Current smoker/tobacco user or quit less than 1 year ago - Skin disorders (psoriasis, etc.) - Pregnant - Taking any medications other than birth control |
Country | Name | City | State |
---|---|---|---|
United States | Georgia State University | Atlanta | Georgia |
Lead Sponsor | Collaborator |
---|---|
Georgia State University |
United States,
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* Note: There are 44 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in skin blood flow response to local heating | Vasodilation in response to painful and non-painful heating of the skin | Baseline (prior to intervention or control) and at the conclusion of the 5-week intervention or control. The post-intervention assessment will be performed no later than 3-5 days after completion of the 5-week intervention or control. |
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