Comparing the Effects of Upper and Lower Body Resistance Training on Pain Sensitivity
NCT ID: NCT05985382
Last Updated: 2025-03-04
Study Results
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View full resultsBasic Information
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COMPLETED
NA
30 participants
INTERVENTIONAL
2023-08-29
2023-10-16
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
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Lower Body Resistance Exercise
Participants will perform a leg extension exercise with weight that is 75% of their estimated 1-repetition maximum (1-RM) for 3 sets of 10 repetitions.
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 perform a shoulder press with weight that is 75% of their estimated 1-repetition maximum (1-RM) for 3 sets of 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.
Interventions
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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.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* 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
18 Years
60 Years
ALL
Yes
Sponsors
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University of Central Florida
OTHER
Responsible Party
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Abigail Wilson
Assistant Professor
Principal Investigators
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Abigail Wilson, PT, DPT, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Central Florida
Locations
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University of Central Florida
Orlando, Florida, United States
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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5
Identifier Type: -
Identifier Source: org_study_id
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