[ONLINE] Safety issues in dementia: A survey of caregivers’ needs and preferences.

  • STATUS
    Recruiting
Updated on 6 October 2020
Investigator
Marian Betz, MD, MPH
Primary Contact
Online27 (3.6 mi away) Contact
+248 other location

Summary

This study is looking for adults who are caregivers for a person with dementia. The study is collecting surveys about caregiver experiences.

Description

 
Study schedule:
-You will complete an online survey. It will take 10-20 minutes.

Study activities may include:
-Using a computer, tablet, or device to access the internet.
-Completing an online survey.

Treatment or experiment details:
-This study is about the needs of dementia caregivers, specifically around being involved with important life decisions.

Additional details:
-The is an online study. If you will like to participate click here

Details
Clinical Study IdentifierTX249062
Last Modified on6 October 2020

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Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age greater than or equal to 18 yrs?
Gender: Male or Female
Do you have any of these conditions: Dementia or *Healthy Volunteers?
You could be eligible for this study if
You are 18 or older
You live in the United States
You are currently a caregiver for a family member or friend with dementia, or have been in the last five years
You are/were involved in the daily care and/or decision-making for your family member or friend with dementia
You may not be eligible for this study if
You have dementia
You do not meet all eligibility criteria, based on screening questions
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How to participate?

Step 1 Connect with a site
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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Step 2 Get screened

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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Step 3 Enroll in the clinical study

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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Step 4 Get your study results

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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