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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date September 2023
Source University of Central Florida
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cold Water Immersion
Cold Water Immersion task of hand
Pain Inducing Stretch
Moderately painful stretch of the neck
Pain Free Stretch
Pain free stretch of the neck

Locations

Country Name City State
United States University of Central Florida Orlando Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Central Florida

Country where clinical trial is conducted

United States, 

Outcome

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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