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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02095327
Other study ID # 20130429
Secondary ID
Status Completed
Phase N/A
First received March 18, 2014
Last updated August 26, 2015
Start date July 2013
Est. completion date June 2015

Study information

Verified date August 2015
Source University of Miami
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of our study is to better understand how caregivers of individuals with dementia cope with their family member's illness. If you are eligible for the study and would like to participate, we will schedule a one-time phone interview, which will last approximately 2 hours for which you will be compensated for your time.


Description:

Eventually, results of this study will be used to develop treatments that will hopefully help caregivers cope more effectively with managing dementia in a loved one.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Caregiver of individual with dementia

- Relative who is 60 years or older with dementia

- Live-in, unpaid caregiver

- Have a working telephone number

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Miami Coral Gables Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Miami

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Depression Measured continuously using the Depression, Anxiety and Stress Scale on a scale of 1 - 56. 3 months No
Secondary Anxiety Measured continuously on the Depression, Anxiety, and Stress Scale on a scale of 1 - 56. 3 months No
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