Attachment Behaviors in Parent Child Dyads Coping with Early Stage Alzheimer’s Disease and Related Dementias.

Updated on 25 January 2022
Accepts healthy volunteers


This study is looking for pairs of participants: a person with Alzheimer’s and their adult child. The study is interested in learning about participants’ experiences in an open-ended way.


Study schedule:
-At the start of the study, you will complete two study visits. Each visit will be 60-90 minutes.
-You will repeat the visits one year later.
-The visits will include interviews, observations, surveys, and blood pressure monitoring.

Study activities may include:
-Completing interview-style conversations.
-Interacting with study personnel.
-Completing surveys.
-Having your blood pressure checked.

Treatment or experiment details:
-There is no treatment being tested in this study.
-The study is interested in learning about your experiences with emotional support in the context of Alzheimer’s and caregiving.

Additional details:
-Study visits can be arranged on evenings, days, or weekends. Parking is free, and transportation is available.

Condition Alzheimer's Disease, Alzheimer's Disease, *Healthy Volunteers
Clinical Study IdentifierTX249120
Last Modified on25 January 2022


Yes No Not Sure

Inclusion Criteria

You could be eligible for this study if
You speak English or Spanish
You can participate in the study as a pair. The pair consists of
A person with Alzheimer’s; and
Their adult child
You may not be eligible for this study if
You do not meet all study criteria, based on screening questions
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.

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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.

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