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Resistance Training and Cardiometabolic Health

Primary Purpose

Insulin Sensitivity, Endothelial Dysfunction, Blood Pressure

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
High Load/Low Rep Resistance Training
Low Load/High Rep Resistance Training
Sponsored by
Arizona State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Insulin Sensitivity focused on measuring insulin sensitivity, muscle, strength, resistance training, strength training, vascular function, arterial stiffness, glucose tolerance

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Male and female
  • 18-55 years of age
  • BMI 25-40
  • No recent history of starting a structured exercise program or diet in the last 3 months

Exclusion Criteria:

  • Current smoker and/or recreational drug user
  • Answers "yes" to one or more questions on the Physical Activity Readiness Questionnaire
  • Diagnosed diabetes, heart disease
  • History of anabolic steroid use in the past six months
  • Taking medications for treatment of diabetes, heart disease, and hypertension.
  • Orthopedic or musculoskeletal contraindications to resistance training
  • Unwilling to follow any aspect of the study protocol including blood sampling and weight training

Sites / Locations

  • Arizona State University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Resistance Training 1

Resistance Training 2

Wait-list control

Arm Description

Participants will perform resistance training with high training loads and low repetitions (high load/low rep resistance training).

Participants will perform resistance training with low training loads and high repetitions (Low load/high rep resistance training).

This group will be offered the option of participating in either experimental group after the study is completed.

Outcomes

Primary Outcome Measures

Arterial Stiffness
Measured via pulse wave velocity

Secondary Outcome Measures

Insulin Sensitivity
Measured via oral glucose tolerance testing (OGTT)
Endothelial Function
Measured via flow mediated dilation (FMD)
Cardiac echocardiography
Measured using ultrasound
Isokinetic Strength
Measured via dynamometry
Isometric Strength
Measured via dynamometry
Hexokinase
Measured via skeletal muscle biopsies
Insulin signaling proteins
Measured via skeletal muscle biopsies
Muscle Volume
Measured via ultrasonography
Body Composition
Measured via Dual X-Ray Absorptiometry (DXA)
Central Systolic Pressure
Measured via Pulse Wave Analysis
Central Diastolic Pressure
Measured via Pulse Wave Analysis

Full Information

First Posted
October 13, 2017
Last Updated
April 14, 2021
Sponsor
Arizona State University
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1. Study Identification

Unique Protocol Identification Number
NCT03325933
Brief Title
Resistance Training and Cardiometabolic Health
Official Title
Resistance Training and Cardiometabolic Health
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Terminated
Why Stopped
COVID-19
Study Start Date
September 21, 2017 (Actual)
Primary Completion Date
August 31, 2020 (Actual)
Study Completion Date
August 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Arizona State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will investigate the relationship between resistance training load and repetitions on cardiometabolic outcomes. The primary objective of this clinical trial is to determine whether high load or low load resistance exercise training affects arterial stiffness in overweight or obese men and women. Our secondary objectives are to investigate the effects of high and low load RT on vascular function, cardiac structure, and markers of insulin sensitivity. Finally, we are going to preliminarily explore the effects of resistance training on intestinal bacteria.
Detailed Description
While it has been firmly established that aerobic exercise training is an effective modality for managing cardiometabolic disease risk, the influence of resistance training (RT) is not as well characterized. It is well established that RT improves muscular strength, size, cross sectional area, and bone mineral density. Alterations in muscle fiber type, glycolytic and oxidative enzyme profile, skeletal muscle proteins, and rates of protein synthesis also occur in response to RT and are obtained from skeletal muscle biopsies. Data from quasi-experimental studies suggest that moderate-to-high repetition RT with lower training loads may positively affect skeletal muscle proteins (Glucose Transporter Type 4 (GLUT4), Hexokinase 2 (HK2), and Adenylate kinase 2 (AK2) involved in insulin signaling in non-diabetic, obese men. However, data on high load, low rep RT on these variables is lacking. Thus, we will collect skeletal muscle biopsies to determine if changes in insulin signaling skeletal muscle proteins are present in response to both training with both high and low training loads. There is also a body of evidence suggesting that RT may improve VO2peak values in individuals with low baseline VO2peak values via a possible increase in capillary density, however, results are currently mixed. Low VO2peak values in overweight and obese individuals are positively associated with high risk of cardiovascular and all-cause mortality. Thus, we will measure VO2peak values to determine if (A) starting previously untrained obese individuals with RT can also improve VO2peak and (B) potential changes in VO2peak are load dependent. RT has also been reported to improve insulin sensitivity and central pressure. Additionally, aerobic exercise training may positively influence alterations in the intestinal microbiome, with no currently available evidence on the effects of RT, Although RT has been shown to be beneficial for improving arterial stiffness and insulin sensitivity, most of the available literature is based on protocols prescribing moderate-to-high repetitions and thus lower training loads. Thus, the effects of prescribing higher training loads on the aforementioned variables are not fully understood. Increased arterial stiffness (as characterized by carotid-femoral pulse wave velocity (PWV) and augmentation index) is a clinical marker for cardiovascular disease and an independent risk factor for adverse cardiovascular events and all-cause mortality. Increased arterial stiffness has is positively associated with insulin resistance and type II diabetes. In the early stages of insulin resistance, peripheral insulin action, which occurs primarily in the skeletal muscle is impaired. This leads to a compensatory increase in insulin release in order to maintain glucose homeostasis, thus leading to hypertrophy of the pancreatic β cells. During the early stages of insulin resistance, fasting glucose levels will remain normal, with hyperglycemia manifesting in the later stages. Chronic hyperinsulinemia and hyperglycemia in turn cause increases in the renin-angiotensin aldosterone system as well expression of the angiotensin type I receptor in vascular tissue, thus stimulating VSMC proliferation, which leads to an increase in arterial stiffness. Chronic hyperglycemia and/or type II diabetes can lead to an increase in the production of advanced glycation end products (AGEs), which are proteins or lipids that become glycated due to exposure to glucose. Excessive production of AGEs can lead to an increase in collagen cross linking in the vascular walls, which thus leads to an increase in arterial stiffness. Thus, it appears that increases in arterial stiffness occur due to perturbations in pulsatile shear and flow, which leads to abnormal turnover of scaffolding proteins, specifically excessive collagen production, and the proliferation of VSMCs, which results in a stiffer vasculature. This is exacerbated by the insulin resistant and/or hyperglycemic state due to an increase in local activity of the RAAS and expression of angiotensin I receptor activation in the vascular wall and an increase in age production, which leads to an increase in VSMCs and collagen cross-linking, respectively, thus further contributing to the development of a stiffer vasculature. These structural changes can have deleterious downstream consequences that include ischemic heart disease, myocardial infarction, and heart failure. Current studies on the effects of RT on arterial stiffness have reported mixed results. It has been suggested that training with higher loads may cause greater increases in stiffness than training with lower loads due to greater acute elevations in blood pressure that occur with high load RT. Case control studies have reported that resistance trained young and middle aged non obese men demonstrated higher levels of arterial stiffness when compared to their aged-matched counterparts. Alternative cross-sectional studies reported that muscular strength was inversely related with arterial stiffness. Follow-up randomized control trials (RCT) investigated changes in arterial stiffness after several months of RT in non-obese, resistance training naïve adults. Improvements in central pressure, in the absence of changes in PWV, have been reported in non-diabetic obese adults after 12 weeks of RT but the study lacked an effective control group. Additionally, improvements in insulin sensitivity in non-diabetic obese males after 12 weeks of RT but was not a randomized controlled trial (RCT). Improvements in endothelial function has also been reported after six months of progressive RT that included both moderate and high training loads. This is significant because endothelial dysfunction is a downstream consequence of increased arterial stiffness, and thus an improvement in endothelial function, as measured by relative flow mediated dilation (%FMD), in response to RT is a reflects an improvement in vascular function, which is unlikely to occur in conjunction with an increase in vascular stiffness. To our knowledge, there are no current published RCTs on the effects of high load RT that have measured both arterial stiffness and endothelial function. This study will follow up on previous studies by comparing the effects of two distinct RT protocols (high load vs low load) on arterial stiffness as, measured by PWV and augmentation index, and endothelial function, as measured by %FMD, to a nonexercising control group. A body of literature exists to suggest that morphological changes of the left ventricle take place in response to resistance training. Case control studies have reported that elite resistance trained athletes demonstrate evidence of left ventricular wall thickening. The increase in left ventricular wall thickness is referred to as concentric hypertrophy, which occurs in response to a chronic increase in afterload. This occurs in the presence of increased arterial stiffness, uncontrolled hypertension, and aortic stenosis, all of which can lead to heart failure (HF). RT induced concentric hypertrophy appears to be a physiological training adaptation, similar to the eccentric hypertrophy that takes place in response to aerobic training, and thus does not appear to be deleterious. Furthermore, current RCTs on the effects of RT on morphological changes of the LV suggest that this adaptation does not always occur or may occur in response to specific training volumes, frequencies, intensities, and/or over a longer training duration. Since the main outcome of this study is arterial stiffness, which is a precursor for concentric hypertrophy of the LV, we will also measure left ventricular wall thickness to see if A) morphological changes in the LV take place and B) if LV morphological changes are influenced by training load. Thus, it appears that moderate training loads are shown to improve insulin sensitivity in obese individuals. This is significant because insulin resistance is a precursor to increases in arterial stiffness. However, the effects of training with higher loads on insulin sensitivity is a current gap in the literature. It has been previously proposed that high load RT may reduce arterial compliance and/or lead to concentric hypertrophy of the left ventricular walls. However, current evidence suggests that both moderate and high training loads improve endothelial function, without negatively affecting the left ventricular wall. Since endothelial dysfunction is a negative downstream consequence of an increase in arterial stiffness, it is unlikely that it would improve in conjunction with an increase in stiffness. Thus, this study will be the first to measure all of these variables to determine if and how they are influenced by training load. The intestinal human microbiome is a recent target of interest due to its role in metabolic disease risk. Current evidence reports a link between cardiometabolic diseases and changes in the intestinal microbiota. The effects of exercise training on changes in the intestinal microbiome is also currently under investigation. Evidence in rat models currently suggest that voluntary and controlled aerobic exercise training is associated with favorable changes in the gut microbiome. However, human studies on the effects of exercise on the intestinal microbiome are currently lacking. . The purpose of this study is to investigate the effects and potential differences between high load and low load RT on arterial stiffness. Based on the above described gaps in the literature the current study will serve as a follow up RCT to previous studies and will further explore the link between RT, arterial stiffness, and insulin sensitivity. From an exploratory stand-point we will examine changes if any in the gut microbiome following resistance training versus control. The proposed study will serve as a follow up RCT to investigate the differences between high load and low load RT on markers of arterial stiffness and insulin sensitivity. This study will also serve as the first RCT to investigate the long-term effects of RT in the intestinal microbiome. Studies investigating the effects of high load/low repetition RT on cardiometabolic biomarkers are currently lacking, with the current body of literature focusing on the effects of moderate and low loads and high repetitions, with limited data on the effects of high load RT.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insulin Sensitivity, Endothelial Dysfunction, Blood Pressure
Keywords
insulin sensitivity, muscle, strength, resistance training, strength training, vascular function, arterial stiffness, glucose tolerance

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
62 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Resistance Training 1
Arm Type
Experimental
Arm Description
Participants will perform resistance training with high training loads and low repetitions (high load/low rep resistance training).
Arm Title
Resistance Training 2
Arm Type
Experimental
Arm Description
Participants will perform resistance training with low training loads and high repetitions (Low load/high rep resistance training).
Arm Title
Wait-list control
Arm Type
No Intervention
Arm Description
This group will be offered the option of participating in either experimental group after the study is completed.
Intervention Type
Other
Intervention Name(s)
High Load/Low Rep Resistance Training
Intervention Description
Participants will be prescribed High Load/Low Rep resistance training.
Intervention Type
Other
Intervention Name(s)
Low Load/High Rep Resistance Training
Intervention Description
Participants will be prescribed Low Load/High Rep resistance training.
Primary Outcome Measure Information:
Title
Arterial Stiffness
Description
Measured via pulse wave velocity
Time Frame
Change from Baseline Pulse Wave Velocity at 12 weeks
Secondary Outcome Measure Information:
Title
Insulin Sensitivity
Description
Measured via oral glucose tolerance testing (OGTT)
Time Frame
Change from Baseline Matsuda Index at 12 weeks
Title
Endothelial Function
Description
Measured via flow mediated dilation (FMD)
Time Frame
Change from Baseline %FMD at 12 weeks
Title
Cardiac echocardiography
Description
Measured using ultrasound
Time Frame
Changes in systolic and diastolic parameters from baseline to 12 weeks
Title
Isokinetic Strength
Description
Measured via dynamometry
Time Frame
Change from Baseline isokinetic strength at 12 weeks
Title
Isometric Strength
Description
Measured via dynamometry
Time Frame
Change from Baseline Isometric strength at 12 weeks
Title
Hexokinase
Description
Measured via skeletal muscle biopsies
Time Frame
Change from Baseline in insulin signalling proteins at 12 weeks
Title
Insulin signaling proteins
Description
Measured via skeletal muscle biopsies
Time Frame
Change from Baseline in insulin signaling proteins at 12 weeks
Title
Muscle Volume
Description
Measured via ultrasonography
Time Frame
Change from Baseline Muscle Volume at 12 weeks
Title
Body Composition
Description
Measured via Dual X-Ray Absorptiometry (DXA)
Time Frame
Change from Baseline body composition at 12 weeks
Title
Central Systolic Pressure
Description
Measured via Pulse Wave Analysis
Time Frame
Change from Baseline Central Systolic Pressure at 12 weeks
Title
Central Diastolic Pressure
Description
Measured via Pulse Wave Analysis
Time Frame
Change from Baseline Central Systolic Pressure at 12 weeks
Other Pre-specified Outcome Measures:
Title
Maximal Oxygen Consumption
Description
Measured via VO2peak testing using an integrated metabolic system.
Time Frame
Change from Baseline VO2peak at 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male and female 18-55 years of age BMI 25-40 No recent history of starting a structured exercise program or diet in the last 3 months Exclusion Criteria: Current smoker and/or recreational drug user Answers "yes" to one or more questions on the Physical Activity Readiness Questionnaire Diagnosed diabetes, heart disease History of anabolic steroid use in the past six months Taking medications for treatment of diabetes, heart disease, and hypertension. Orthopedic or musculoskeletal contraindications to resistance training Unwilling to follow any aspect of the study protocol including blood sampling and weight training
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Siddhartha S Angadi, PhD
Organizational Affiliation
Arizona State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Arizona State University
City
Phoenix
State/Province
Arizona
ZIP/Postal Code
85004
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
This data will be used primarily for a doctoral dissertation project as well as manuscript publication.
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Resistance Training and Cardiometabolic Health

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