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

  • STATUS
    Recruiting
Updated on 25 January 2022
Accepts healthy volunteers

Summary

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.

Description

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.

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

Eligibility

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.

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