Aging Clinical Trial
Official title:
The Impact of High Intensity Interval Training on Inflammatory State and Immune Function in Elderly Individuals
Verified date | February 2017 |
Source | Duke University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
PURPOSE: The purpose of this study is to investigate whether High Intensity Interval Training
(HIIT)can improve the health and wellbeing of pre-diabetic elderly adults. In particular,
there is specific interest in describing the effects of an interval exercise program on
inflammatory state and immune function.
DESIGN: Subjects will be sedentary, 65 to 80 years old adults, with prediabetes as defined by
fasting plasma glucose (100 to 125 mg/dl). Before and after a 10-12 week High Intensity
Interval Exercise training program subjects will undergo several tests including: 1) a
maximal treadmill test, 2) an Oral Glucose Tolerance Test, 3) muscle biopsy, 4) body
composition, 5) several physical function tests and 6) other health related measures
including lung function, arterial stiffness and several blood measures (e.g. liver enzymes,
kidney function).
DATA ANALYSES & SAFETY ISSUES: As there are no comparison groups, data analyses will consist
of performing paired t-tests on pre and post exercise training values for each of the
measurement variables of interest. In addition, the data will be used to provide power
calculations for future grant proposals. High Intensity Interval Training is a very safe
exercise modality. The regular use of vigorous intensity exercise intervals have been used
extensively in exercise training. In fact, the exercise intervals will start at levels lower
and will be of shorter duration than were used during the maximal exercise test. They will
then be carefully and slowly made to be more challenging as each subject is able to safely
tolerate.
HYPOTHESIS: The investigators hypothesize that HIIT will result in significant improvements
in markers of inflammation, immune system markers and other health-related risk factors.
Status | Completed |
Enrollment | 30 |
Est. completion date | November 14, 2016 |
Est. primary completion date | November 14, 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 65 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Age 65-80 years - Prediabetic - Fasting plasma glucose is 100 - 125 on two separate days - Able to walk for 2 minutes or more without stopping - LDL Cholesterol = 190; Triglycerides < 600; - Blood Pressure = 160/90 - Inactive: Exercise < 2 days per week - Medications: Stable use of all medications = three months Exclusion Criteria: - Smoker: tobacco use within the last 12 months - Dieting or intending to diet; not weight stable = six months (weight change < 5 pounds) - Use of confounding inflammatory medications: aspirin, ibuprofen, naproxen (NSAIDS - nonsteriodal anti-inflammatory drugs) - History of diabetes, heart disease or taking medications for those conditions - History of hypertension (high blood pressure) not controlled with medication - Unwillingness to undergo muscle biopsies and all other study testing, or to continuously participate in exercise training for 12 weeks. - Inability to give blood continuously through a catheter (please notify the study nurse of any difficulties you have had in the past when having your blood drawn; the study nurse will determine whether you are excluded for this reason) - Unwillingness to conduct ALL exercise sessions at the fitness facility during research study staff supervised times. - Orthopedic limitations, musculoskeletal disease and/or injury Due to the nature of the study, persons with known joint, muscle or other orthopedic limitations that restrict physical activity may be excluded. - Able to decide if you want to take part in the study - Lack of transportation to the exercise and testing facilities |
Country | Name | City | State |
---|---|---|---|
United States | Duke Center for Living | Durham | North Carolina |
Lead Sponsor | Collaborator |
---|---|
Duke University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in Physical Function outcome measures composite score | Peak VO2, 400 meter walk time, short physical performance battery (SPPB) | baseline and following exercise training, approximately 10-12 weeks | |
Primary | Change in inflammatory markers in plasma | baseline and following exercise training, approximately 10-12 weeks | ||
Primary | Change in inflammatory markers in muscle | baseline and following exercise training, approximately 10-12 weeks | ||
Primary | Change in immune markers in peripheral blood | baseline and following exercise training, approximately 10-12 weeks | ||
Primary | Change in immune markers in muscle | baseline and following exercise training, approximately 10-12 weeks | ||
Secondary | Change in Metabolic Syndrome risk factors composite score | Classic and additional Metabolic Syndrome measures include: blood pressure, waist circumference, triglycerides, HDL, fasting glucose; plus liver and kidney function, insulin sensitivity, glucose tolerance, etc... | baseline and following exercise training, approximately 10-12 weeks |
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