- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03330587
Living Alone in Old Age With Cognitive Impairment
The purpose of this study is to better understand the experience of living alone in older age with cognitive impairment.
We recruit adults 55+ living alone with cognitive impairment such as Alzheimer's disease or mild cognitive impairment.
This study investigates the priorities and concerns of older adults living alone with cognitive impairment. Participants are interviewed 5 times for one hour in their homes within 3 months at a time that works for them.
Study Overview
Status
Detailed Description
The purpose of this study is to better understand the experience of living alone in older age with cognitive impairment. This knowledge is important to design programs that are appropriate. Dr. Elena Portacolone, an Assistant Professor from the Institute of Health and Aging is the study researcher.
Study participants are interviewed by Elena at a time and place convenient to them, usually their home. Interviews are audio recorded and last around one hour. Study participants are interviewed five times within 3 months.
After the interview, a transcriptionist will type into a computer the recording and will remove personal names. The sound recording will then be destroyed.
Participants can stop being in the study at any time.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
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California
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San Francisco, California, United States, 94705
- Institute for Health & Aging
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Living alone
- Medical diagnosis of Alzheimer's disease or mild cognitive impairment
Exclusion Criteria:
- Living in nursing homes, assistive living facilities.
- Alcohol abuse
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ethnographic interviews
Time Frame: One hour
|
Questions that follow the train of thought of study participants
|
One hour
|
Collaborators and Investigators
Investigators
- Principal Investigator: Elena Portacolone, PhD MPH MBA, University of California, San Francisco
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01AG069147 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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