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ACTIV- Exercise Intervention in Healthy Young Men

ACTIVValidation of a Paradigm for the Evaluation of Compounds That Activate Mitochondrial Biogenesis in Skeletal Muscle

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00401791
Enrollment
40
Registered
2006-11-22
Start date
2006-11-30
Completion date
2016-10-31
Last updated
2022-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Insulin Resistance

Brief summary

The study is designed to compare muscle energy capacity in men with obesity or diabetes as compared to athletes. This study will also enable researchers to determine whether MRS can replace muscle biopsy for this type of assessment.

Detailed description

Skeletal muscle mitochondrial defects are a sine qua non of insulin resistance in patients with type 2 diabetes mellitus (T2DM), obese and subjects with family history of T2DM (FH+). Exercise increases mitochondrial capacity whereas lipid infusion or high fat diet decreases genes involved in mitochondrial biogenesis. In this study 2 cohorts will be involved: Cohort I (athletes, T2DM and obese) and Cohort II (healthy with FH+ or without FH- family history of T2DM). This randomized, parallel arm clinical trial will consist of 4 periods: screening, stabilization (3 days), baseline (for Cohort I and II) and exercise period (14 days, only for Cohort II). The overall objective of the study is to validate a paradigm for the evaluation of compounds and drugs that activate mitochondrial biogenesis in skeletal muscle. In Specific Aim 1 we will compare and contrast biopsy and MRS power to detect differences in mitochondrial capacity in 78 subjects: athletes (N=10), FH- (N=24), FH+ (N=24), obese (N=10) and T2DM (N=10). In Specific Aim 2 we will compare mitochondrial changes in response to exercise in subjects FH - vs. FH + subjects. In Specific Aim 3 we will determine if HFD impairs mitochondrial changes in response to exercise in FH+ subjects. In Specific Aim 4 we will determine the role of mitochondrial capacity in metabolic flexibility and insulin sensitivity in T2DM, obese, FH+, FH- and athlete subjects.

Interventions

BEHAVIORALExercise

* Interval Exercise Training: Each interval training session will start with 10 minutes of warm up and will end with 10 minutes of cool down period at 40% VO2 peak. Training duration, intensity and number of exercise bout will increase with the progression of training period * Aerobic training: Each endurance training session will start with 5 minutes of warm up and will end with 5 minutes of cool down at 40% VO2 peak. Subjects will exercise at 70% VO2 peak for 45 minutes on day 3 and 5, for 55 minutes on day 8 and 10, and for 35 minutes on day 14 using a bicycle ergometer.

Sponsors

Pennington Biomedical Research Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
25 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

T2DM group: * Men aged 25-35 * BMI \> 30 kg/m2 * Sedentary lifestyle determined by activity index questionnaire (not involved in regular exercise program) and accelerometer data. * Are willing to eat only foods provided by Pennington for the study period * Diagnosed with T2DM defined by one or more of the following: * fasting plasma glucose \> 126 mg/dL at entry * a two-hour OGTT glucose \> 200mg/dL * current medication for T2DM Obese group: * Men aged 25-35 * BMI \> 30 kg/m2 * Sedentary lifestyle activity index questionnaire (not involved in regular exercise program) and accelerometer data. * Are willing to eat only foods provided by Pennington for the study period FH+ group: * Men aged 25-35 * One parent diagnosed with T2DM * fasting insulin \> 10mIU/ml (\> 50th %tile) * BMI between 22 and 30 kg/m2 * Sedentary lifestyle activity index questionnaire (not involved in regular exercise program) and accelerometer data. * Are willing to exercise every day for the study period * Are willing to eat only foods provided by Pennington for the study period FH- group: * Men aged 25-35 * Parents and grandparents were not diagnosed with T2DM * Fasting insulin \< 10mIU/ml (\< 50th %tile) * BMI between 22 and 30 kg/m2 * Sedentary lifestyle activity index questionnaire (not involved in regular exercise program) and accelerometer data. * Are willing to exercise for the study period * Are willing to eat only foods provided by Pennington for the study period Athlete group: * Men aged 25-35 * Maximal oxygen uptake \> 60 ml/kg.min * Are engaged in minimum of 1.5 h of aerobic exercise 3 times/ week * Are willing to eat only foods provided by Pennington for the study period

Exclusion criteria

* Abnormal resting or exercise ECG * Significant renal, cardiac, liver, lung, or neurological disease (controlled hypertension is acceptable if baseline bp \< 140/90 on medications) * Use of drugs known to affect energy metabolism or body weight: including, but not limited to: orlistat, sibutramine, ephedrine, phenylpropanolamine, corticosterone, etc * Alcohol or other drug abuse * Smoking * Gait problems * Unwilling or unable to abstain from caffeine (48h) prior to metabolic rate measurements * Unwilling or unable to eat all study foods * Increased liver function tests at baseline (AST/ALT/GGT/or alkaline phosphatase greater than 2.5 times the upper limit of normal) * Metal objects that would interfere with the measurement of body composition /MRS such as implanted rods, surgical clips, etc * NYHA class III/IV CHF is an exclusionary cardiac condition * history of deep vein thrombosis (DVT) or pulmonary embolism (PE) * varicose veins * major surgery on the abdomen, pelvis, or lower extremities within previous 3 months * cancer (active malignancy with or without concurrent chemotherapy) * rheumatoid disease * bypass graft in limb * known genetic factor (Factor V Leiden, etc) or hypercoagulable state * diagnosed peripheral arterial or vascular disease, or intermittent claudication * family history of primary DVT or PE (pulmonary embolism) * peripheral neuropathy

Design outcomes

Primary

MeasureTime frame
To compare/ contrast the power of skeletal muscle biopsy vs. MRS to detect differences in mitochondrial capacitybaseline and after intervention

Secondary

MeasureTime frame
To compare mitochondrial changes in response to exercise in subjects FH - vs. FH + subjects by skeletal muscle biopsy and MRSbaseline and after intervention
To determine if HFD impairs mitochondrial changes in response to exercise in the FH + group by muscle biopsy and MRS.baseline and after intervention
To determine the role of mitochondrial capacity in metabolic flexibility and insulin sensitivitybaseline and after intervention

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026