Comparing the Effects of Different Types of Exercise on Glucose Handling

Insulin Sensitivity Clinical Trial

Official title:

Comparing the Effects of Different Types of Exercise on Glucose Handling and Muscle Metabolism in Young Males and Females

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06217679
• Other study ID #: ORE #22477
• Status: Completed
• Phase: N/A
• Start date: May 1, 2018
• Est. completion date: October 31, 2019

Study information

• Verified date: January 2024
• Source: University of Waterloo
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the proposed study is to compare the acute effects of different types of exercise modalities on glucose handling in young, healthy males and females. The exercise modalities that will be compared include: a high intensity interval exercise (HIIE) protocol, a moderate intensity continuous exercise (MICE) protocol and a low-load, high-repetition (LL-HR) resistance exercise protocol.

Description:

The purpose of this study is to compare the effects of different exercise modalities (High intensity interval exercise, Moderate intensity continuous exercise, and Low-load-high repetition resistance exercise) on blood sugar control in young healthy, males and females. To test this theory, a sugar challenge (oral glucose tolerance test - OGTT) will be performed during the pre-testing visit to determine the baseline blood sugar response. An OGTT will also be performed 2 hours after each single exercise session to determine how each type of exercise affects the blood sugar response. Investigators will take multiple blood samples throughout the trial to allow us to measure blood sugar, insulin and concentrations and oxidative stress. Muscle biopsies will be taken before and after each exercise bout so that investigators can examine the underlying mechanisms that contribute to the effectiveness of the different types of exercise on blood sugar control. Investigators will also use an ultrasound to measure factors related to of cardiovascular health such as artery stress and vascular conductance during the exercise bouts. Direct benefits of this study include characterizing sex differences of blood sugar handling after single exercise sessions. This study could have direct benefits on deterring the effectiveness of different forms of exercise on blood sugar levels.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 24
• Est. completion date: October 31, 2019
• Est. primary completion date: October 31, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 30 Years

Eligibility

Inclusion Criteria:

• In order to participate in this study, participants must be a healthy man or woman between the ages of 18 and 30 years.

Exclusion Criteria:

• Presence of chronic health condition(s) [i.e. metabolic (i.e. Type 1 or type 2 diabetes), cardiovascular (i.e hypertension), respiratory (i.e. chronic pulmonary obstructive disorder) or digestive (i.e. ulcerative colitis) disorders.
• Are pregnant, or suspect that they may be pregnant, or nursing
• Inability to complete the single exercise sessions.
• Regularly participate in cardiovascular (>3 sessions/week) or resistance training (>2 sessions/week) exercise.
• Have an allergy to local anesthetic (or family history of allergy)
• Have undergone a barium swallow or an infusion of a contrast agent in the past 3 weeks
• Are taking prescription anti-coagulant or anti-platelet medications (e.g., warfarin, heparin, clopidogrel)
• Inability to exercise as suggested by the get active questionnaire (GAQ)
• BMI > 27 kg/m2

Related Conditions & MeSH terms

• Glycemic Control
• Insulin Resistance
• Insulin Sensitivity
• Sex Differences

Intervention

Other:
• Control Oral Glucose Tolerance Test
control oral glucose tolerance test
• Mixed Exercise
exercise performed in randomized order

Locations

Country	Name	City	State
Canada	University of Waterloo	Waterloo	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
University of Waterloo

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Blood insulin change	To assess the effect of sex and exercise on basal and post-exercise blood insulin	120mins
Primary	Blood glucose change	To assess the effect of sex and exercise on basal and post-exercise blood glucose.	120mins
Primary	Blood c-peptide change	To assess the effect of sex and exercise on basal and post-exercise blood c-peptide.	120mins
Primary	Insulin sensitivity change	Assess the changes in insulin sensitivity pre to post exercise	120mins
Secondary	TBC1 domain family member 4 change (TBC1D4)	examine protein content changes from pre to post exercise	35mins
Secondary	TBC1 domain family member 1 change (TBC1D1)	examine protein content changes from pre to post exercise	35mins
Secondary	protein kinase B change	examine protein content changes from pre to post exercise	35mins
Secondary	5' adenosine monophosphate-activated protein kinase change	examine protein content changes from pre to post exercise	35mins
Secondary	glucose transporter 4 change (GLUT4)	examine protein content changes from pre to post exercise	35mins
Secondary	estrogen concentration	to assess the differences in estrogen concentration between males and females	30mins
Secondary	progesterone concentration	to assess the differences in progesterone concentration between males and females	30mins