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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02068612
Other study ID # 1R01AG043452-01A1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 2014
Est. completion date December 3, 2018

Study information

Verified date March 2020
Source University of Colorado, Boulder
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Physiological and neurocognitive changes experienced as a result of increasing age may influence socioemotional functioning and economic behaviors, yet, the mechanisms through which these changes occur are not well understood. Studies have also shown that aerobic exercise may protect against age-related cognitive decline in other domains. This research is designed to test the hypothesis that aerobic exercise will enhance social, emotional and economic functioning in older adults, and that these effects will occur via the effect of exercise on neurocognitive structure and function assessed via magnetic resonance imaging (MRI). Advancing our knowledge of the mechanisms that influence emotional, social and economic functioning could inform the development of targeted treatments and prevention programs for older adults.


Recruitment information / eligibility

Status Completed
Enrollment 317
Est. completion date December 3, 2018
Est. primary completion date November 13, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years and older
Eligibility Inclusion Criteria:

- Age 25-35 for younger adults, and age 60 or over for older adults

- Sedentary (i.e., < 60 minutes per week of moderate physical activity in the past 6-months)

- Able to make fewer than 3 errors on the Pfeiffer Mental Status192

- Willing to accept random assignment to condition (older adults)

- Physically capable of safely engaging in moderate exercise activity (i.e., no injuries, physical impairments, or pre-existing contraindications) as assessed by a study physician

- Able to successfully complete a maximal exercise test without evidence of cardiac or other abnormalities

- Planning to remain in the Boulder-Denver metro area for the next 4 months (older adults)

Exclusion Criteria:

- Are a heavy smoker (>20 pack years)

- Are diabetic

- Have a body size exceeding the capacity of the magnetic resonance imaging machine (approximately 23" in diameter)

- Are on antipsychotic medications

- Are currently under treatment for any psychiatric disorder, including clinical depression, Alzheimer's, or dementia

- Are currently pregnant

- Have magnetic resonance imaging contraindications (i.e., non-removable metallic implants, claustrophobia, traumatic brain injury, current pregnancy, etc.)

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Moderate Intensity Continuous Training+Interval Training

Low Intensity Continuous Training


Locations

Country Name City State
United States University of Colorado Boulder Boulder Colorado

Sponsors (1)

Lead Sponsor Collaborator
University of Colorado, Boulder

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cognitive Function Functional connectivity is measured via having participants lie in a magnetic resonance imaging scanner and passively stare at a centrally-positioned fixation crosshair for 8 min while their brain activity is recorded.
Executive function will be measured with 3 tasks characterized by the three domains of executive function: updating, shifting, and inhibition. For updating, we will utilize the Keep Track task,for shifting, we will use the Category Switch Task, and for inhibition we will use the Stroop task.
4 months
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