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Enhancing Function in Later Life: Exercise and Functional Network Connectivity (FORCE)

U

University of Colorado Boulder (CU)

Status

Completed

Conditions

Aging

Treatments

Behavioral: Moderate Intensity Continuous Training+Interval Training
Behavioral: Low Intensity Continuous Training

Study type

Interventional

Funder types

Other

Identifiers

NCT02068612
1R01AG043452-01A1

Details and patient eligibility

About

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.

Enrollment

317 patients

Sex

All

Ages

25+ years old

Volunteers

Accepts Healthy Volunteers

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.)

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

317 participants in 2 patient groups

MICT + IT
Experimental group
Description:
Moderate Intensity Continuous Training+Interval Training
Treatment:
Behavioral: Moderate Intensity Continuous Training+Interval Training
LICT
Active Comparator group
Description:
Low Intensity Continuous Training
Treatment:
Behavioral: Low Intensity Continuous Training

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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