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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05985382
Other study ID # 5
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 29, 2023
Est. completion date October 16, 2023

Study information

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

Clinical Trial Summary

Resistance exercise may immediately lessen the perception of pain. The purpose of this study is compare the effects of an upper body exercise to a lower body exercise on the perception of pain (pressure pain threshold).


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date October 16, 2023
Est. primary completion date October 16, 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 - medical conditions known to affect sensation, such as: uncontrolled diabetes or neurological conditions - any contraindication to the application of ice, including: 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 within the past 6 months - unable to perform exercise portions of the study - unable to attend three sessions - pregnant

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Lower Body Resistance Exercise
Participants will complete a leg extension exercise with weight equivalent to 75% of their estimated 1-repetition maximum 3 sets, 10 repetitions.
Upper Body Resistance Exercise
Participants will complete a leg extension exercise with weight equivalent to 75% of their estimated 1-repetition maximum 3 sets, 10 repetitions.

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 Heat Pain Threshold A thermode will gradually warm up from 32 degrees Celsius until the participant reports the sensation changes from comfortable warmth to slightly unpleasant pain. The temperature at threshold will be recorded. Heat pain threshold will be applied to the quadriceps, deltoid, and low back immediately before and immediately after each exercise (pre/post).
Primary Pressure Pain Threshold Pressure will be applied with a digital algometer. Pressure will be gradually increased until the participant reports the sensation changes from comfortable pressure to slightly unpleasant pain. The pressure at threshold will be recorded. Pressure pain threshold will be applied to the quadriceps, deltoid, and low back immediately before and immediately after each exercise (pre/post).
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