Zinnia All Day Application - Clinical Trial

What is the Purpose of this Study?

Copilot said: If you choose to join this study, you will first complete a short screening. You will then use Zinnia TV at home for about one month. After that, you will attend one in-person study visit in Durham, North Carolina, lasting about 2.5 hours. During the visit, you will try the new Zinnia All Day app, complete activities, and take part in an interview to share your thoughts and feedback. Participants who complete the visit will receive payment for their time.

What is the Condition Being Studied?

Copilot said: This study is for adults who care for a family member or loved one with Alzheimer’s disease or a related dementia. Researchers want to learn more about the experiences and needs of caregivers and find ways to better support people who provide care for individuals living with these conditions.

Who Can Participate in the Study?

Adults may be able to join this study if they are 18 years of age or older and provide care for a family member or loved one age 55 or older who has memory loss. Participants must currently use Zinnia TV or be willing to use it for about one month before the study visit. They must also be able to attend an in-person study visit in Durham, North Carolina, without the person they care for.

Age Group
Adults

What is Involved?

This study is testing the Zinnia All Day app, a tool designed to help people with Alzheimer’s disease and related dementias stay on track with daily routines and activities. Researchers want to find out if the app is easy to use and helpful for caregivers. Participants will provide feedback about their experience using the app, and that information will be used to improve it for people living with dementia and their care partners.

Study Details

Full Title
Zinnia All Day: An application for mobile devices and connected TVs to assist care partners promote routine in activities of daily living in persons with Alzheimer's Disease and Related Dementias
Principal Investigator
Protocol Number
IRB: PRO00120379
NCT: NA
Phase
Phase N/A
ClinicalTrials.gov
Enrollment Status
Open for Enrollment
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