Last updated: December 23, 2022
Sponsor: Rutgers, The State University of New Jersey
Overall Status: Active - Recruiting
Phase
2/3
Condition
Diabetes Prevention
Diabetes And Hypertension
High Cholesterol (Hyperlipidemia)
Treatment
N/AClinical Study ID
NCT04817787
Pro2020002029
5R01HL130296-04
Ages 40-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Male or female ≥ 40 and ≤ 80 years old
- Has a body mass index ≥ 25 and ≤ 47 kg/m^2
- Not diagnosed with Type 2 diabetes
- Not currently engaged in > 150 min/wk of exercise
- At minimum, subjects will have abdominal obesity (increased waist circumference asdefined below) and may have any additional National Cholesterol Education AdultTreatment Panel III Metabolic Syndrome criteria:
- Increased waist circumference (≥ 102 cm in men; ≥ 88 cm in women)
- Elevated triglycerides (≥ 150 mg/dl), or on medication for treating the condition
- Reduced HDL-cholesterol (< 40 mg/dl in men, < 50 mg/dl in women), or on medication fortreating the condition
- High blood pressure (≥ 130 mmHg systolic or ≥ 85 mmHg diastolic), or on medication fortreating the condition
- Elevated fasting glucose (≥ 100 mg/dl), or on medication for treating the condition
- Subjects currently taking medications that affect heart rate and rhythm (i.e.calcium-channel blockers, nitrates, alpha- or beta-blockers)
- Other major risk factors to be noted based on the Framingham Risk Score:
- HbA1c 5.7-6.4%
- LDL > 130 mg/dL
- Family history of type 2 diabetes (immediate family, i.e. parent/sibling)
- History of gestational diabetes
- History of Polycystic Ovarian Syndrome
- Family history of pre-mature cardiovascular disease (immediate family i.e.parent/sibling) before 55 for males or 65 for females that can include heart attack,peripheral arterial disease, abdominal aortic aneurysm, symptomatic carotid arterydisease or clinical coronary heart disease)
- Age ( > 45 years old for men; > 55 years old for women)
- Black/African American, Mexican, Asian, and/or Hispanic
Exclusion
Exclusion Criteria:
- Morbidly obese patients (BMI > 47 kg/m^2) and overweight/lean patients (BMI < 27kg/m^2)
- Evidence of type 1 diabetes and diabetics requiring insulin therapy
- Subjects who have not been weight stable (> 2 kg weight change in past 3 months)
- Subjects who have not been recently active (> 30 min of moderate/high intensityexercise, 2 times/week)
- Subjects who are smokers or who have quit smoking < 5 years ago
- Subjects prescribed metformin or have taken metformin within 1 year
- Subjects with abnormal estimated glomerular filtration rate (eGFR)
- Hypertriglyceridemic (> 400 mg/dl) and hypercholesterolemic (> 260 mg/dl) subjects
- Hypertensive ( > 160/100 mmHg)
- Subjects with a history of significant metabolic, cardiac, congestive heart failure,cerebrovascular, hematological, pulmonary, gastrointestinal, liver, renal, orendocrine disease or cancer that in the investigator's opinion would interfere with oralter the outcome measures, or impact subject safety
- Pregnant (as evidenced by positive pregnancy test) or nursing women
- Subjects with contraindications to participation in an exercise training program
- Currently taking active weight suppression medication (e.g. phentermine, orlistat,lorcaserin, naltrexone-bupropion in combination, liraglutide, benzphetamine,diethylpropion, phendimetrazine)
- Known hypersensitivity to perflutren (contained in Definity microbubbles)
- Subjects who are considered non-English speaking individuals
Study Design
Total Participants: 80
Study Start date:
November 28, 2017
Estimated Completion Date:
May 31, 2025
Study Description
Connect with a study center
Loree Gymnasium
New Brunswick, New Jersey 08901
United StatesActive - Recruiting
New Jersey Institute for Food, Nutrition & Health
New Brunswick, New Jersey 08901
United StatesActive - Recruiting
Rutgers Clinical Research Center
New Brunswick, New Jersey 08901
United StatesActive - Recruiting

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