Living Alone in Older Age with Cognitive Impairment.

  • STATUS
    Recruiting
Updated on 15 September 2020
cognitive impairment
mild cognitive impairment

Summary

This study is looking for people who live alone and have mild cognitive impairment or Alzheimer’s. The study is interested in learning about participants’ experiences in an open-ended way.

Description

This study is looking for people who live alone and have mild cognitive impairment or Alzheimer’s. The study is interested in learning about participants’ experiences in an open-ended way.
Study schedule:
-You will meet with the researcher at a location that is convenient to you.
-There will be about 5 meetings. Each meeting will be about one hour.

Study activities may include:
-Talking with the researcher about your experiences living alone.

Treatment or experiment details:
-This study is interested in learning about your experiences in an open-ended way.
-There is no treatment or experiment being tested in this study.

Additional details:
-You will receive a $30 gift card for participating.

Details
Condition Alzheimer's Disease, Mild Cognitive Impairment
Clinical Study IdentifierTX249057
Last Modified on15 September 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have any of these conditions: Alzheimer's Disease or Mild Cognitive Impairment?
You could be eligible for this study if
You have a medical diagnosis of Alzheimer’s or mild cognitive impairment
You live alone—that is, without family members, friends, housemates, or professional caregivers
You may not be eligible for this study if
You live in an institution such as an assisted living facility or a nursing home
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How to participate?

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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.

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

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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.

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

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