Virtual Patient Behavioral Response Training for Family Caregivers

  • STATUS
    Recruiting
  • participants needed
    150
  • sponsor
    Photozig, Inc.
Send
Updated on 19 February 2024
See if I qualify
alzheimer's disease
dementia

Summary

Our study is designed to help caregivers of someone with Alzheimer's Disease and related dementia to understand and deal with the difficult behaviors of a person with dementia.

Description

The goal of this study is to develop and evaluate the Caring Response mobile app, containing a training that builds skills and stimulates practice. The investigators are evaluating different materials, which may encourage caregiver participation, enable user interaction, and promote better assimilation of concepts. The research team is designing the program to help to enhance caregivers' skills to deal with difficult behaviors, reduce distress, and improve quality of life.

Details
Condition Dementia, Dementia, Alzheimer's Disease, Alzheimer's Disease
Age 18years - 100years
Treatment Caring Response App, Traditional Educational/Resources Program
Clinical Study IdentifierNCT04489303
SponsorPhotozig, Inc.
Last Modified on19 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

Care for an individual with Alzheimer's Disease or other dementia
Own a smartphone or tablet and have Internet access
Minimum age of 18 years old
Spend at least 8 hours/week caring for a person with dementia

Exclusion Criteria

Severe psychological or physical illness
Inability to read and follow English instructions
High level of depressive symptoms
Unwillingness to participate in all aspects of the study
Clear my responses
Read more

How to participate?

Step 1 Connect with a study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

First name*
Last name*
Email*
Phone number*
Other language

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

Browse trials for

alzheimer's disease
dementia

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