- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04298710
Effects of Arm Cycling and Leg Cycling on Postprandial Blood Glucose Levels in Healthy Persons
August 18, 2020 updated by: Tongyu Ma, Franklin Pierce University
A Comparison Between the Effects of Different Muscle Groups on Blood Glucose Levels at the Postprandial Status in College Students
The literature has shown that exercise is effective in decreasing blood glucose levels.
However, it remains less clear if there is any difference between muscle groups regarding the glucose-lowering effects of exercise.
The purpose of this study is to examine the differences in blood-glucose level changes in response to exercise that involves different muscle groups.
Study Overview
Status
Terminated
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
4
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New Hampshire
-
Rindge, New Hampshire, United States, 03461
- Franklin Pierce University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 79 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Apparently healthy persons
- Age 18 years or above
Exclusion Criteria:
- Cardiovascular diseases
- Pulmonary diseases
- Metabolic diseases
- Other contraindications to exercise
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Arm Cycling
Arm cycling on an arm crank ergometer for 20 minutes at light to moderate intensity.
30 minutes before the exercise, participants will consume 60g of carbohydrates mixed with plain water.
|
20 minutes of arm cycling exercise at light to moderate intensity.
|
|
Experimental: Leg Cycling
Leg cycling on a leg cycling ergometer for 20 minutes at light to moderate intensity.
30 minutes before the exercise, participants will consume 60g of carbohydrates mixed with plain water.
|
20 minutes of leg cycling exercise at light to moderate intensity.
|
|
Placebo Comparator: Sitting
Participants will remain seated after carbohydrates consumption.
|
Remain seated for 20 minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Postprandial glucose levels
Time Frame: one hour after the carbohydrates intake
|
one hour after the carbohydrates intake
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Tongyu Ma, Ph.D., Franklin Pierce University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 9, 2020
Primary Completion (Actual)
August 15, 2020
Study Completion (Actual)
August 15, 2020
Study Registration Dates
First Submitted
March 4, 2020
First Submitted That Met QC Criteria
March 4, 2020
First Posted (Actual)
March 6, 2020
Study Record Updates
Last Update Posted (Actual)
August 20, 2020
Last Update Submitted That Met QC Criteria
August 18, 2020
Last Verified
August 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CD02252020
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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