Healthy Clinical Trial
Official title:
Pain Modulatory Profiles in Stretching in Healthy Participants
NCT number | NCT05891353 |
Other study ID # | 4 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 20, 2023 |
Est. completion date | September 27, 2023 |
Verified date | September 2023 |
Source | University of Central Florida |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to characterize immediate changes in pain sensitivity during stretching to the point of pain, stretching in a pain free range, and a cold water immersion task. Participants will attend three sessions during which they will undergo pain sensitivity assessment and complete the assigned intervention.
Status | Completed |
Enrollment | 30 |
Est. completion date | September 27, 2023 |
Est. primary completion date | September 27, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Pain Free Exclusion Criteria: - Non-English speaking - Regular use of prescription pain medications - Current or history of chronic pain condition - Currently taking blood-thinning medication - Any blood clotting disorder, such as hemophilia - Systemic medical condition known to affect sensation, such as uncontrolled diabetes or neurological conditions - Any contraindication to the application of ice, such as: uncontrolled hypertension, cold urticaria, cryoglobulinemia, paroxysmal cold hemoglobinuria, circulatory compromise - Not physically ready to exercise without a medical exam as indicated by the Physical Activity Readiness Questionnaire Plus (PAR-Q+) - Surgery, injury, or fracture to the neck or upper extremity within the past 6 months - Unable to perform the stretch - Unable to attend all three sessions |
Country | Name | City | State |
---|---|---|---|
United States | University of Central Florida | Orlando | Florida |
Lead Sponsor | Collaborator |
---|---|
University of Central Florida |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Pressure Pain Threshold | A pressure algometer will be applied between the first and second toe until the pressure sensation first becomes painful. Pressure pain threshold is applied between each one minute interval of the intervention. | Change in PPT is applied between minutes 1,2,3,4 of the intervention and for up to 15 minutes after each intervention. |
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