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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03330587
Other study ID # R01AG069147
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date March 1, 2016
Est. completion date May 31, 2025

Study information

Verified date November 2023
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 60
Est. completion date May 31, 2025
Est. primary completion date February 20, 2024
Accepts healthy volunteers No
Gender All
Age group 55 Years and older
Eligibility 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 Design


Locations

Country Name City State
United States Institute for Health & Aging San Francisco California

Sponsors (1)

Lead Sponsor Collaborator
University of California, San Francisco

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ethnographic interviews Questions that follow the train of thought of study participants One hour
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