[ONLINE] Daily Reflections of Dementia Caregivers

  • STATUS
    Recruiting
Updated on 28 January 2021
Investigator
Dr. Carolyn Pickering
Primary Contact
Online163 (7.8 mi away) Contact
+252 other location

Summary

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
210-560-3075
pickeringc@uthscsa.edu

Study Website:

Description

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.

Details
Condition *Healthy Volunteers
Clinical Study IdentifierTX249126
Last Modified on28 January 2021

Eligibility

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
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How to participate?

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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.

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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.

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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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