[ONLINE] Daily Reflections of Dementia Caregivers

Updated on 25 February 2022
cognitive impairment
mild cognitive impairment
Accepts healthy volunteers


This study is looking for caregivers of family members who have mild cognitive impairment or dementia. This is a survey study that is interested in learning about caregivers’ experiences.

Contact Person
Dr. Carolyn Pickering

Study Website:


Study schedule:
At the start of the study:
-You will complete online surveys. The surveys take about 45 minutes.
-You will complete a daily diary online or by phone. The diary will be every day for three weeks. It will take about six minutes each day.
During the study:
-You will repeat the study-start activities one or more times.
The study will end after about a year.

Study activities may include:
-Completing online surveys.
-Completing daily diaries online or by phone.

Treatment or experiment details:
-There is no treatment or experiment being tested in this study. The study is interested in the experiences of caregivers.
-The surveys are about changes in health, finances, and the household. The daily diary is about emotions, behaviors, and activities.

Additional details:
-You will receive a modest gift for completing the study activities.

Condition Dementia, Mild Cognitive Impairment, *Healthy Volunteers
Clinical Study IdentifierTX249126
Last Modified on25 February 2022


Yes No Not Sure

Inclusion Criteria

You could be eligible for this study if
You are 18 or older
You are fluent in English or Spanish
You have reliable access to the internet or a phone
You are a caregiver for a spouse or family member who has mild cognitive impairment or dementia
You help your care recipient with daily activities
You live with your care recipient and/or share cooking facilities with them
You may not be eligible for this study if
Your care recipient will move to a nursing home or similar facility within the next six months
You, or your care recipient, are terminally ill
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

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Primary Contact


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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