- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04007926
Mechanisms of Insulin Resistance and Exercise in South Asians
October 7, 2020 updated by: Professor Jason Gill, University of Glasgow
Effects of Exercise Training on Insulin Sensitivity in South Asians at Risk of Diabetes: the Roles of Skeletal Muscle Microvasculature and Mitochondrial Metabolism
This study determines the effect of aerobic and resistance exercise training on whole-body and skeletal muscle insulin sensitivity in south Asians and evaluate the mechanisms which contribute to improvements in insulin sensitivity after exercise training.
Study Overview
Status
Suspended
Conditions
Intervention / Treatment
Detailed Description
South Asians (SA) have 2-4 fold higher risk of type 2 diabetes and develop the disease at lower body weights and younger ages than white Europeans.
Lower cardiorespiratory fitness and capacity for muscle fat oxidation contributes substantially to SAs' greater insulin resistance, the extent to which this can be improved by exercise training is unclear.
This randomised controlled trial will investigate the effects of a 12-week aerobic or resistance exercise training intervention on insulin sensitivity (hyperinsulinaemic-euglycaemic clamp) in South Asian adults (22 control, 22 aerobic exercise group and 22 resistance exercise group).
The study will also explore the mechanisms within skeletal muscle which mediate these changes by evaluating aerobic and resistance exercise-training induced changes: in basal and insulin-stimulated microvascular blood volume (using contrast-enhanced ultrasound); skeletal muscle mitochondrial function; and lipid droplet morphology and spatial interaction with mitochrondria, muscle fibre capillarisation, endothelial content of key enzymes controlling dilation/constriction and GLUT-4 translocation (using confocal immunofluorescence microscopy and transmission electron microscopy methods).
Thus, this work will integrate physiological and molecular data to determine the extent to which exercise training can improve insulin sensitivity in SA and the mechanisms underpinning this improvement.
This knowledge is important for optimising diabetes prevention interventions in SAs and identification of potential novel therapeutic targets.
Study Type
Interventional
Enrollment (Anticipated)
66
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
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Glasgow, United Kingdom, G12 8QQ
- University of Glasgow
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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
30 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Male
- South Asian ethnicity (self-report of both parents of Indian, Pakistani, Bangladeshi or Sri Lankan origin)
- Age 30-65 years
- At least 10% 10-year risk of developing type 2 diabetes, determined using the QDiabetes®2018 risk score (http://qdiabetes.org/2018/index.php)
Exclusion Criteria:
- Female
- Diabetes (physician diagnosed or HbA1c ≥48 mmol/mol on screening)
- History of cardiovascular disease
- Hypertension (taking anti-hypertensives or BP consistently ≥ 150/90 mmHg on screening).
- Regular participation in vigorous physical activity
- Regular participation in resistance exercise
- Current smoking
- Taking drugs or supplements thought to affect carbohydrate or lipid metabolism
- Taking drugs affecting blood clotting (e.g. aspirin)
- Current treatment with anti-obesity drugs
- Any other significant illness that would prevent full participation in the study
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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No Intervention: Control Group
Participants assigned to the control arm of the study will be asked to maintain their normal dietary and exercise habits.
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Experimental: Aerobic exercise group
Participants randomised to the aerobic exercise intervention will undertake a 12-week aerobic exercise training programme.
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Participants will start with 3 x 20 minute exercise sessions in the first week, building up to 5 x 60 minutes of exercise by weeks 9-12 of the intervention, at an intensity of 65-80% of predicted maximum heart rate.
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Experimental: Resistance exercise group
Participants randomised to the resistance exercise intervention will undertake a 12-week aerobic exercise training programme.
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Participants will undertake two supervised sessions per week.
The exercises performed during each session will consist of leg press, calf press, leg extension, leg curl, chest press, shoulder press, lateral pull down and seated row.
Exercises will be performed at 60-80% 1RM.
In weeks 1-2 participants will perform, during each session, a single set of 5-10 repetitions of each exercise (tiring but comfortably achievable) to ensure they are comfortable with the exercises and are performing these in the correct form.
In weeks 3-4 participants will perform, during each session, two sets of each exercise to voluntary muscular failure - defined as not being able to perform single another repetition.
In weeks 5-12 this will progress to 3 sets of each exercise to voluntary muscular failure, in each session.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Whole-body Insulin sensitivity
Time Frame: Change between baseline and 12 weeks.
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Change in whole-body insulin sensitivity measured by hyperinsulinaemic-euglycaemic clamp.
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Change between baseline and 12 weeks.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Insulin-stimulated GLUT4 translocation
Time Frame: Change between baseline and 12 weeks.
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Change in insulin-stimulated GLUT4 translocation in muscle biopsies from vastus lateralis using immunofluorescence microscopy
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Change between baseline and 12 weeks.
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Microvascular blood volume
Time Frame: Change between baseline and 12 weeks.
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Change in fold-increase in insulin stimulated quadriceps muscle blood volume measured using contrast enhanced ultrasound.
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Change between baseline and 12 weeks.
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Muscle mitochondrial function
Time Frame: Change between baseline and 12 weeks.
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Change in mitochondrial function (oxygen consumption rate) in isolated skeletal muscle mitochondria from the vastus lateralis measured using respirometry
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Change between baseline and 12 weeks.
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Lipid droplet content in skeletal muscle
Time Frame: Change between baseline and 12 weeks.
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Change in fibre type-specific (type 1 and type 2) and subcellular-specific (subsarcolemmal and intermyofibrillar) lipid droplet content in muscle biopsies from vastus lateralis using immunofluorescence microscopy
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Change between baseline and 12 weeks.
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Lipid droplet proximity to mitochondria in skeletal muscle
Time Frame: Change between baseline and 12 weeks.
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Change in proportion of lipid droplets in contact with mitochondria in subsarcolemmal and intermyofibrillar compartments of type 1 and type 2 muscle fibres in muscle biopsies from vastus lateralis using immunofluorescence microscopy
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Change between baseline and 12 weeks.
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Microvascular density in skeletal muscle
Time Frame: Change between baseline and 12 weeks.
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Change in fibre-type specific capillarisation in muscle biopsies from vastus lateralis
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Change between baseline and 12 weeks.
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Change in enzymes controlling insulin-mediated increases in perfusion in skeletal muscle
Time Frame: Change between baseline and 12 weeks.
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Change in endothelial specific protein content and phosphorylation of key microvascular enzymes in muscle biopsies from vastus lateralis assessed using quantitative immunofluorescence.
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Change between baseline and 12 weeks.
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Maximal oxygen uptake
Time Frame: Change between baseline and 12 weeks.
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Change in maximal oxygen uptake consumption assessed using continuous incremental uphill walking protocol until volitional exhaustion.
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Change between baseline and 12 weeks.
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Muscle maximal voluntary contraction
Time Frame: Change between baseline and 12 weeks.
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Change in knee extensor muscles maximal voluntary contraction
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Change between baseline and 12 weeks.
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Lower body muscle strength
Time Frame: Change between baseline and 12 weeks.
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Change in 1-RM (one maximal repetition) (kg) for leg press.
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Change between baseline and 12 weeks.
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Upper body muscle strength
Time Frame: Change between baseline and 12 weeks.
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Change in 1-RM (one maximal repetition) (kg) for chest press.
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Change between baseline and 12 weeks.
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Grip strength
Time Frame: Change between baseline and 12 weeks.
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Change in grip strength (kg).
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Change between baseline and 12 weeks.
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Fat mass
Time Frame: Change between baseline and 12 weeks.
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Change in fat mass measured with bioelectrical impedance analysis (BIA).
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Change between baseline and 12 weeks.
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Fat-free mass
Time Frame: Change between baseline and 12 weeks.
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Change in fat-free mass measured with bioelectrical impedance analysis (BIA).
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Change between baseline and 12 weeks.
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Weight
Time Frame: Change between baseline and 12 weeks.
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Change in weight (kg).
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Change between baseline and 12 weeks.
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Waist circumference
Time Frame: Change between baseline and 12 weeks.
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Change in waist circumference (cm)
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Change between baseline and 12 weeks.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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 (Anticipated)
August 1, 2021
Primary Completion (Anticipated)
March 1, 2023
Study Completion (Anticipated)
January 1, 2025
Study Registration Dates
First Submitted
June 28, 2019
First Submitted That Met QC Criteria
July 2, 2019
First Posted (Actual)
July 5, 2019
Study Record Updates
Last Update Posted (Actual)
October 8, 2020
Last Update Submitted That Met QC Criteria
October 7, 2020
Last Verified
October 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 265320
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
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