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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05574413
Other study ID # AEX2022
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 15, 2022
Est. completion date September 1, 2023

Study information

Verified date December 2023
Source University of British Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The immune system helps prevent illness, fights off infections, and repairs damaged tissues following an injury. However, when immune cells remain active for prolonged periods of time - a state known as "chronic inflammation" - they can contribute to the development and progression of chronic diseases like heart disease and diabetes. Exercise can reduce the risk of developing many of these diseases and at least part of the health benefits of exercise are due to the ability of exercise to reduce "chronic inflammation". The inflammation-lowering effects of exercise are typically captured by measuring hormone-like molecules released from immune cells called "cytokines" in the blood. In addition to changes in circulating cytokine levels, exercise may also alter how immune cells respond to these cytokines. How exercise intensity (i.e., how hard you are working during exercise) and pattern (i.e., exercising as a long continuous bout or in short intervals) impact the ability of immune cells to respond to cytokines is not well understood. A better understanding of how exercise intensity and pattern of exercise for reducing chronic inflammation may help determine the best types of exercises for improving health and preventing chronic diseases.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date September 1, 2023
Est. primary completion date August 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - 18-35 years of age - Body mass index between 18.5-30 kg/m^2 - Free of cardiometabolic and autoimmune/inflammatory disease Exclusion Criteria: - Competitive endurance athlete - Cigarette smoker - Currently taking immunomodulatory/anti-inflammatory medications - Currently pregnant

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Moderate intensity continuous exercise
Participants will perform an acute bout of continuous cycling at 70% of the power output at lactate threshold until an energy expenditure of 350 kcal is achieved. Blood samples will be obtained immediately before and immediately, 30, and 90 minutes after exercise.
High intensity continuous exercise
Participants will perform an acute bout of continuous cycling at 10% of the difference between lactate threshold and VO2peak until an energy expenditure of 350 kcal is achieved. Blood samples will be obtained immediately before and immediately, 30, and 90 minutes after exercise.
High intensity interval exercise
Participants will perform an acute bout of interval cycling at at 10% of the difference between lactate threshold and VO2peak until an energy expenditure of 350 kcal is achieved. Blood samples will be obtained immediately before and immediately, 30, and 90 minutes after exercise.
Resting (no exercise) control
Participants will remain in a rested state (i.e., no exercise) for the entire session. Blood samples will be obtained at the same time-points as the exercise sessions.

Locations

Country Name City State
Canada UBC Okanagan Kelowna British Columbia

Sponsors (1)

Lead Sponsor Collaborator
University of British Columbia

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary IL-10 mediated STAT3 phosphorylation Ex vivo leukocyte STAT3 phosphorylation in response to IL-10 treatment Change from pre-exercise to immediately and 90-min post-exercise
Secondary IL-10 mediated TNF-alpha inhibition Ex vivo inhibition of TNF-alpha production in response to IL-10 treatment Change from pre-exercise to immediately and 90-min post-exercise
Secondary IL-6 mediated STAT3 phosphorylation Ex vivo leukocyte STAT3 phosphorylation in response to IL-6 treatment Change from pre-exercise to immediately and 90-min post-exercise
Secondary IL-6 mediated TNF-alpha inhibition Ex vivo inhibition of TNF-alpha production in response to IL-6 treatment Change from pre-exercise to immediately and 90-min post-exercise
Secondary Plasma IL-10 Concentration of IL-10 in plasma samples Change from pre-exercise to immediately, 30-, and 90-min post-exercise
Secondary Plasma IL-6 Concentration of IL-6 in plasma samples Change from pre-exercise to immediately, 30-, and 90-min post-exercise
Secondary Plasma TNF-alpha Concentration of TNF-alpha in plasma samples Change from pre-exercise to immediately, 30-, and 90-min post-exercise
Secondary Hematology panel Complete blood count Change from pre-exercise to immediately, 30-, and 90-min post-exercise
Secondary Extracellular vesicles Concentration of extracellular vesicles in plasma Change from pre-exercise to immediately, 30-, and 90-min post-exercise
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