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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01738568
Other study ID # 12-003357
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2012
Est. completion date February 12, 2015

Study information

Verified date August 2021
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Aging is associated with a loss of brain function and conditions such as dementia and Alzheimer's disease. It is likely that decreased brain metabolism is contributing to the progression of age related degenerative diseases. Aerobic exercise training can increase brain volumes and is associated with decreased risk for degenerative brain conditions. However, little is know about the changes that occur to brain metabolism with aerobic training and aging.


Recruitment information / eligibility

Status Completed
Enrollment 27
Est. completion date February 12, 2015
Est. primary completion date February 12, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Healthy sedentary adults aged 18-30 or 65-80 years of all ethnicities will be eligible. Pregnant women, children, prisoners or other at risk populations will not be recruited. Inclusion Criteria: - Age 18-30 years or 65-80 years Exclusion Criteria: - Body mass index (BMI) >31 kg/m2 - Smoking - Pregnancy - Participation in structured exercise (>2 times per week for 30 minutes or longer) - Cardiovascular, metabolic (type 2 diabetes, fasting plasma glucose at or above 110 mg/dL and untreated hypo- or hyperthyroidism) or renal disease - Orthopedic problems that would keep them from being able to ride an exercise bicycle, lift weights or do a combination of these exercise - Medications that are known to impact on mitochondrial function: Corticosteroids, opiates, benzodiazepines, tricyclic antidepressants, beta blockers, sulfonylureas, insulin, anticoagulants, barbiturates, insulin sensitizers, fibrates (PPAR gamma agonist) - Claustrophobia

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
High intensity aerobic training
High intensity aerobic interval training will be performed 12-weeks. Exercise training will last 1 hour per day, 5 days per week and include high intensity interval cycling at ~70-95% maximum workload for 4 minutes followed by 3 minutes of rest.
Sedentary Control
Sedentary control participants will not perform any regular exercise for 12-weeks.

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Brain Glucose Uptake The investigators will assess brain glucose uptake using positron emission tomography at baseline and following 12-weeks of either aerobic exercise training or sedentary control period. 12 weeks
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