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Clinical Trials/NCT06217679
NCT06217679CompletedNot Applicable

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

University of Waterloo1 site in 1 country24 target enrollmentStarted: May 1, 2018Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
24
Locations
1
Primary Endpoint
Blood insulin change

Study Overview

Brief 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.

Detailed 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 30 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

Arms & Interventions

Control Oral Glucose Tolerance Test

Experimental

This visit will include a baseline OGTT to be used as a pre-exercise baseline measure for each of the arms. Participants will then consume a 75g glucose beverage (Trutol, Thermo Scientific) and blood samples will be drawn at 0, 10, 20, 30, 45, 60, 75, 90 and 120 minutes post consumption.

Intervention: Control Oral Glucose Tolerance Test (Other)

Control Oral Glucose Tolerance Test

Experimental

This visit will include a baseline OGTT to be used as a pre-exercise baseline measure for each of the arms. Participants will then consume a 75g glucose beverage (Trutol, Thermo Scientific) and blood samples will be drawn at 0, 10, 20, 30, 45, 60, 75, 90 and 120 minutes post consumption.

Intervention: Mixed Exercise (Other)

High intensity interval exercise (HIIE)

Experimental

Participants performed a High intensity interval exercise (HIIE) bout which includes 10 x 1 min at 90% maximum heart rate (HRmax) with 5 min warm up and 5 min cool down at 50watts (low state steady cycling). 90mins following the exercise bout participants will undergo another oral glucose tolerance test.

Intervention: Control Oral Glucose Tolerance Test (Other)

High intensity interval exercise (HIIE)

Experimental

Participants performed a High intensity interval exercise (HIIE) bout which includes 10 x 1 min at 90% maximum heart rate (HRmax) with 5 min warm up and 5 min cool down at 50watts (low state steady cycling). 90mins following the exercise bout participants will undergo another oral glucose tolerance test.

Intervention: Mixed Exercise (Other)

Moderate intensity continuous exercise (MICE)

Experimental

Participants performed a Moderate intensity continuous exercise (MICE) bout which includes 30 min at 65% maximal aerobic capacity (VO2max). 90mins following the exercise bout participants will undergo another oral glucose tolerance test.

Intervention: Control Oral Glucose Tolerance Test (Other)

Moderate intensity continuous exercise (MICE)

Experimental

Participants performed a Moderate intensity continuous exercise (MICE) bout which includes 30 min at 65% maximal aerobic capacity (VO2max). 90mins following the exercise bout participants will undergo another oral glucose tolerance test.

Intervention: Mixed Exercise (Other)

Low-load, high-repetition resistance exercise (LL-HR)

Experimental

Participants performed a Low-load, high-rep resistance exercise (LL-HR) bout which includes a whole body resistance exercise bout, 3 sets at 30% maximum strength (1RM) for leg press, knee extension, hamstring curl, lat pulldown, shoulder press, chest press, 20-25 reps, last set to failure. 90mins following the exercise bout participants will undergo another oral glucose tolerance test.

Intervention: Control Oral Glucose Tolerance Test (Other)

Low-load, high-repetition resistance exercise (LL-HR)

Experimental

Participants performed a Low-load, high-rep resistance exercise (LL-HR) bout which includes a whole body resistance exercise bout, 3 sets at 30% maximum strength (1RM) for leg press, knee extension, hamstring curl, lat pulldown, shoulder press, chest press, 20-25 reps, last set to failure. 90mins following the exercise bout participants will undergo another oral glucose tolerance test.

Intervention: Mixed Exercise (Other)

Outcomes

Primary Outcomes

Blood insulin change

Time Frame: 120mins

To assess the effect of sex and exercise on basal and post-exercise blood insulin

Insulin sensitivity change

Time Frame: 120mins

Assess the changes in insulin sensitivity pre to post exercise

Blood glucose change

Time Frame: 120mins

To assess the effect of sex and exercise on basal and post-exercise blood glucose.

Blood c-peptide change

Time Frame: 120mins

To assess the effect of sex and exercise on basal and post-exercise blood c-peptide.

Secondary Outcomes

  • TBC1 domain family member 1 change (TBC1D1)(35mins)
  • protein kinase B change(35mins)
  • TBC1 domain family member 4 change (TBC1D4)(35mins)
  • estrogen concentration(30mins)
  • progesterone concentration(30mins)
  • 5' adenosine monophosphate-activated protein kinase change(35mins)
  • glucose transporter 4 change (GLUT4)(35mins)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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