Non-Immersive Virtual Reality as a Cognitive Rehabilitation

  • STATUS
    Recruiting
Updated on 15 September 2020
moderate dementia

Summary

The study is looking for people over 65 who have mild-to-moderate dementia.  The study is testing a computer game.

Description

Study schedule:
There will be seven study visits.
-Visit 1 is at the study center.  It will take 1-2 hours.
-Visits 2-5 are at your home.  Each one will be about 30 minutes.
-Visits 6 and 7 are at the study center.  Each one will take 1-2 hours.

The study will end after about two months.

Study activities may include:
-Doing paper-and-pencil tests of memory and thinking.
-Performing everyday tasks, such as making a meal, at the study center.
-Doing computer tasks.
-Completing questionnaires.

Treatment or experiment details:
-During the study, you will use a computer game.  Research assistants can provide help if needed.
-The study is interested in whether the computer game can improve everyday functioning.

Additional details:

-Participants will receive $75 for completing the study.



Details
Condition Dementia, Dementia, *Healthy Volunteers
Clinical Study IdentifierTX247502
Last Modified on15 September 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

You could be eligible for this study if
You are 65 or older
You have mild-to-moderate dementia
You are fluent in English
You have a ‘study partner’—a family member, friend, or caregiver—who would be willing to answer questions about you
You may not be eligible for this study if
You have a significant neurological, medical, or psychiatric condition, including seizures, brain tumor, history of stroke, history of head injury, major infections, cancer, kidney disease, severe vitamin deficiency, schizophrenia, bipolar disorder, severe depression, or severe anxiety
You have significant impairments of your vision, hearing, or ability to move
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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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