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Exercise in Asymptomatic Pre-Alzheimer's Disease Pilot Study

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Mayo Clinic

Status

Completed

Conditions

Alzheimer's Disease Prevention

Treatments

Behavioral: Aerobic vs. Non-Aerobic exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT01834716
12-002817

Details and patient eligibility

About

Researchers are trying to determine if cognitively normal subjects undergoing a moderate aerobic exercise program will accumulate less amyloid-ß (Aβ) concentration in their brain than subjects undergoing a non-aerobic exercise program, and further evaluating the safety and imaging characteristics of florbetapir F 18, the radioactive drug that will allow us to image changes in the brain amyloid-ß (Aβ).

Full description

After screening assessments have been completed, subjects will be randomized into one of two groups: aerobic exercise group and non-aerobic exercise group. All subjects will be trained on the Physical Activity Scale for the Elderly (PASE), using the Body Media armband, and exercise diary. Subjects will also complete an online food questionnaire.

Subjects assigned to the aerobic exercise group will work with an exercise trainer who will provide individual training (six half hour sessions) until they are proficient at the use of the equipment and understand goals. Subjects will return to Brooks Family YMCA at their convenience, but at a minimum of four times per week. Subjects will complete the exercise journal daily and the Physical Activity Scale for the Elderly (PASE) questionnaire on a monthly basis.

Subjects assigned to the non-aerobic exercise group will attend supervised classes on toning and stretching at a minimum of four times per week. Subjects will complete the exercise journal daily and the Physical Activity Scale for the Elderly (PASE) questionnaire on a monthly basis.

Enrollment

16 patients

Sex

All

Ages

65+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

  • 65 years of age or older.
  • Not diagnosed with memory problems.
  • Do not exercise in which you sweat and/or raise your pulse rate more than 30 minutes two times per week.
  • Able to walk ten blocks (about one mile).
  • Willing to participate in weekly exercise classes at the Brooks YMCA for six months.
  • Able to have an MRI and CT/PET scan.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

16 participants in 2 patient groups

Aerobics exercise
Experimental group
Description:
Participants in this group will be randomized to aerobics exercise (the equivalent of walking briskly for 50 minutes three times per week).
Treatment:
Behavioral: Aerobic vs. Non-Aerobic exercise
Non-Aerobics Exercise
Experimental group
Description:
Participants in this group will be randomized to a non-aerobics (attending classes of toning and stretching a minimum of three times per week) exercise group.
Treatment:
Behavioral: Aerobic vs. Non-Aerobic exercise

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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