- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06897995
Aerobic Exercise on Platelet Mitochondrial Function
The Effects of Aerobic Exercise on Aerobic Fitness and Platelet Mitochondrial Bioenergetics
This study explores how exercise affects blood platelets and their role in clotting. Regular exercise can influence how efficiently clots form in the body. Intense exercise tends to increase platelet activity and the expression of certain molecules on their surface, while moderate exercise can decrease this activity. Since platelets are responsible for blood clotting, understanding how they function can be crucial.
Understanding Platelets:
Platelets are blood cells that help in clotting. The mitochondria within platelets help regulate their function. If these mitochondria don't work properly, it can lead to issues with clotting. By examining how exercise changes platelet mitochondria, the investigators can potentially identify important markers for health and disease progression.
Study Design:
This study compares two types of exercise routines: circuit training and stationary bicycle training.
Participants will be randomly assigned to one of the two groups:
Circuit Training Group: This involves moving through different exercise stations within a set time, targeting various body parts. It's tailored for those who might find regular exercise challenging, helping to reduce fatigue in any single area and improve overall fitness.
Bicycle Training Group: This involves exercising on a stationary bike. Both exercise groups will engage in high-intensity interval training for about 40 minutes, five times a week, over six weeks.
Assessment: Participants will undergo tests to measure endurance and physical function.
Blood Sampling: Blood will be drawn before and after the exercise tests, with 20 milliliters taken from the arm vein. Blood samples will also be collected at the start and end of a 6-week intervention, totaling 80 milliliters throughout the study. This helps the investigators analyze how platelets are affected by exercise.
This study is designed to help the investigators better understand how different types of exercise can benefit platelet function and overall health. Participanting in this research could contribute to the knowledge about how could exercise influence blood clotting and related health conditions. Participants' involvement will include exercise routines or maintaining your current lifestyle, along with simple blood tests. Participation is highly valuable and can help pave the way for new health insights and treatments.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Taoyuan, Taiwan, 333
- Chang Gung University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Willing to sign a written informed consent form.
- Ages 18 to 28.
- No regular exercise habit (defined as exercising 2 times a week or less, for 60 minutes or less each time, for over a year).
Exclusion Criteria:
- Overweight (BMI > 24) or underweight (BMI < 19).
- Smoked within the past year, or consumed alcohol in the past month exceeding 60 grams of alcohol per occasion.
- Having metabolic, circulatory, respiratory, or immune-related diseases or risk factors such as diabetes, hyperlipidemia, hypertension, heart disease, clotting disorders, asthma, allergies, autoimmune diseases, etc.
- Long-term use of any nutritional supplements or medications (e.g., vitamins, pain relievers, aspirin, traditional Chinese medicine).
- Significant knee injuries within the past year (e.g., ligament damage, fractures).
- Students and laboratory staff taught, assessed, evaluated, tested, or appraised by the principal investigator of this study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Circuit training group
|
Participants in the exercise groups were trained five times a week for six weeks.
The regimen began with a 5-min warm-up and ended with a 5-min cool-down, both at 40% of heart rate reserved (HRR).
The circuit training participants were trained for three bouts of 10-min moderate-intensity exercise (60% of HRR) with 1-min rest intervals at a stationary ergometer, a rowing machine, and an elliptical trainer, respectively.
The cycling training group was trained on an ergometer for three bouts of 10-min cycling on a stationary ergometer.
|
|
Active Comparator: Cycle ergometer group
|
Participants in the exercise groups were trained five times a week for six weeks.
The regimen began with a 5-min warm-up and ended with a 5-min cool-down, both at 40% of heart rate reserved (HRR).
The circuit training participants were trained for three bouts of 10-min moderate-intensity exercise (60% of HRR) with 1-min rest intervals at a stationary ergometer, a rowing machine, and an elliptical trainer, respectively.
The cycling training group was trained on an ergometer for three bouts of 10-min cycling on a stationary ergometer.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Platelet mitochondrial respiration
Time Frame: baseline and 2 days upon the completion of the 6-week intervention
|
The mitochondrial OXPHOS and ET capacities in platelets were analyzed.
|
baseline and 2 days upon the completion of the 6-week intervention
|
|
Cardiopulmonary fitness
Time Frame: baseline and 2 days upon the completion of the 6-week intervention
|
Graded Exercise Test was performed on an ergometer.
|
baseline and 2 days upon the completion of the 6-week intervention
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 202300538B0
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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