An Insole and Ankle Device for Monitoring Cognitive Decline in Individuals at Risk for Alzheimer's Disease and/or Alzheimer's Disease Related Dementias (AD/ADRD)

Lead Sponsor

HealthPartners Institute

Collaborators

Age

55 - No limit years

Sex

ALL

Healthy Volunteers

Yes

•Age 55 or older
•Ability to ambulate without the use of an assistive device. For this study, we will assume participants are ambulatory if they can complete the functional outcome measures (i.e., TUG) without the use of an assistive device
•Ability to understand and provide informed consent, or has a legally authorized representative (LAR) to provide consent on their behalf
•Ability to don and doff the insole and leg module independently or have assistance for the duration of the study

•Non-English Speaking
•Use of ankle-foot orthosis for ambulation that prevents use of the system
•Self-reported acute thrombophlebitis including deep vein thrombosis
•Untreated lymphedema or lesion of any kind, swelling, infection, inflamed area of skin or eruptions on or near product use (foot and ankle)
•Untreated fractures in the foot and ankle
•Any other significant medical condition that may affect participation or performance in the study, as determined by investigators