Comparing the Effects of Different Types of Exercise on Glucose Handling
1 other identifier
interventional
24
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started May 2018
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 31, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
October 31, 2019
CompletedFirst Submitted
Initial submission to the registry
January 8, 2024
CompletedFirst Posted
Study publicly available on registry
January 22, 2024
CompletedFebruary 6, 2024
January 1, 2024
1.5 years
January 8, 2024
February 2, 2024
Conditions
Outcome Measures
Primary Outcomes (4)
Blood insulin change
To assess the effect of sex and exercise on basal and post-exercise blood insulin
120mins
Blood glucose change
To assess the effect of sex and exercise on basal and post-exercise blood glucose.
120mins
Blood c-peptide change
To assess the effect of sex and exercise on basal and post-exercise blood c-peptide.
120mins
Insulin sensitivity change
Assess the changes in insulin sensitivity pre to post exercise
120mins
Secondary Outcomes (7)
TBC1 domain family member 4 change (TBC1D4)
35mins
TBC1 domain family member 1 change (TBC1D1)
35mins
protein kinase B change
35mins
5' adenosine monophosphate-activated protein kinase change
35mins
glucose transporter 4 change (GLUT4)
35mins
- +2 more secondary outcomes
Study Arms (4)
Control Oral Glucose Tolerance Test
EXPERIMENTALThis 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.
High intensity interval exercise (HIIE)
EXPERIMENTALParticipants 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.
Moderate intensity continuous exercise (MICE)
EXPERIMENTALParticipants 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.
Low-load, high-repetition resistance exercise (LL-HR)
EXPERIMENTALParticipants 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.
Interventions
control oral glucose tolerance test
exercise performed in randomized order
Eligibility Criteria
You may qualify if:
- In order to participate in this study, participants must be a healthy man or woman between the ages of 18 and 30 years.
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Waterloo
Waterloo, Ontario, N2L 3G1, Canada
Related Publications (1)
Beaudry KM, Surdi JC, Pancevski K, Tremblay C, Devries MC. Greater glycemic control following low-load, high-repetition resistance exercise compared with moderate-intensity continuous exercise in males and females: a randomized control trial. Appl Physiol Nutr Metab. 2024 Jul 1;49(7):943-955. doi: 10.1139/apnm-2023-0353. Epub 2024 Mar 22.
PMID: 38518263DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 8, 2024
First Posted
January 22, 2024
Study Start
May 1, 2018
Primary Completion
October 31, 2019
Study Completion
October 31, 2019
Last Updated
February 6, 2024
Record last verified: 2024-01