Aging Well with Independence Using Sensors in the Environment

  • STATUS
    Recruiting
Updated on 25 February 2022
Accepts healthy volunteers

Summary

This study is looking for people over the age of 65 who are in good health. The study is testing a technology system for in-home monitoring of routine daily activities.

Description

Study schedule:
There will be four study visits: one per year. Each study visit will be 2-3 hours long. During these visits:
-You will answer questions about your health.
-You will have cognitive assessments.
-Each week, you will complete an online health survey at home.
-Each month, you will complete an online memory test at home.
-Additionally, unobtrusive sensor technologies will be installed in your home during the duration of the study.
The study will end after about four years.

Study activities may include:
-Answering questions about your health and completing cognitive assessments. This may be in the form of interview-style conversations, paper-and-pencil questionnaires, computer tests, and/or other activities.
-Completing online questionnaires.
-Completing online memory tests.
-Using sensor technologies in your home.

Details
Condition Mild Cognitive Impairment,*Healthy Volunteers
Clinical Study IdentifierTX249066
Last Modified on25 February 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

You could be eligible for this study if
You are 65 or older
You are in relatively good health
You live at home (alone or with a partner)
You drive a car at least once per week
You have a ‘study partner’—a family member or friend—who would be willing to answer questions about you
<b>You may not be eligible for this study if:</b>
You have dementia
You have had a stroke
You have a serious or chronic medical condition
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

0/250

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Browse trials for

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note