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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00753363
Other study ID # AGCG-003-05F
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2007
Est. completion date November 29, 2012

Study information

Verified date March 2018
Source VA Office of Research and Development
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Persistent low-grade inflammation and impaired fibrinolysis, are independent predictors of several chronic diseases highly prevalent in the older Veteran population including cardiovascular disease (CVD), stroke, and diabetes. Inflammation is likely to be a causative underlying mechanism of insulin resistance. Lifestyle changes such as weight loss and physical activity are advocated for the treatment of these chronic diseases and endpoints, and data are emerging which suggest that these treatments may be beneficial, in part, due to their anti-inflammatory effects. Identification of effective therapies that reduce chronic inflammation for Veterans is important given the widespread adverse health effects of a chronically elevated inflammatory state.


Description:

This study will compare the effects of 6 month trial of aerobic exercise (AEX) vs. weight loss (WL) in older individuals on:

1. adipokine secretion and expression (tumor necrosis factor alpha, adiponectin);

2. adipose tissue and skeletal muscle inflammatory proximal receptor expression (adiponectin and tumor necrosis factor alpha expression) and signaling pathways; and

3. whether the changes in signal transduction are associated with changes in peripheral whole body insulin sensitivity by a hyperinsulinemic-euglycemic clamp.

The prevention and treatment of insulin resistance, the metabolic syndrome, and their CVD complications through exercise and weight loss could improve Veterans' health and reduce health care costs. Knowledge of their effectiveness has important implications for the cardiovascular health of Veterans given the widespread adverse health effects of chronic inflammation on vascular biology, skeletal muscle function and insulin action.


Recruitment information / eligibility

Status Completed
Enrollment 119
Est. completion date November 29, 2012
Est. primary completion date November 29, 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 45 Years to 80 Years
Eligibility Inclusion Criteria:

- Male and Female

- 45-80 yrs of age

- Non-smoking for one year

- Body mass index greater than 20 kg/m2 and less than 50 kg/m2

- Menopause over 1 year

Exclusion Criteria:

- Symptomatic heart disease, coronary artery disease, congestive heart failure, or uncontrolled hypertension (blood pressure over 180/100 mm Hg) unless medically stabilized

- Currently being treated for active cancer

- Type 1 diabetes; Insulin or oral agent treatment for diabetes, poorly controlled diabetes fasting blood glucose over 160 mg/dl

- Allergic to lidocaine

- Untreated dyslipidemia with National Cholesterol Adult Treatment Panel III 10 year cardiac risk score greater than 10%, or receiving triglyceride lowering meds

- Other systemic disorders that are not medically treated and stable

- Taking beta-blockers, oral steroids, warfarin or any other medications interfering with fat/muscle metabolism that may not be safely discontinued temporarily for specific procedures (ie for 72 hours prior)

- Abnormal response to exercise test (ST segment depression greater than 2mm, chest pain, significant arrhythmias, extreme shortness of breath, cyanosis, exercising BP above 240/120mm Hg, or other contraindications to exercise) *requires follow up treatment w/ primary MD for continued participation in study

- Abnormal liver function

- Abnormal renal function

- Chronic pulmonary disease

- Anemia hematocrit below 35 mg/dl, platelets below 100,000/cm3

- Mini-mental state exam below 24, dementia or unstable clinical depression by exam

- Aerobically trained with maximal oxygen consumption greater than 2 standard deviations above age-adjusted mean

- Exercise group only: History of cerebrovascular disease (by medical history) with symptoms limiting the ability to exercise

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Weight Loss
6 months of weight loss
Aerobic Exercise Training
6 months of aerobic exercise training

Locations

Country Name City State
United States Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD Baltimore Maryland

Sponsors (3)

Lead Sponsor Collaborator
VA Office of Research and Development Johns Hopkins University, University of Maryland

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Insulin Sensitivity Insulin resistance is defined as a reduction in glucose utilization rate elicited by a given insulin concentration. Glucose utilization is measured during a three hour hyperinsulinemic-euglycemic clamp and is presented as a measure of insulin sensitivity. This is one of the most sophisticated methods to measure insulin sensitivity. Baseline and 6 month
Secondary Body Weight Baseline and 6 month
Secondary Fitness Maximal oxygen consumption (VO2max) on a treadmill Baseline and 6 month
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