- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01782157
Smart Environment Technology for Longitudinal Behavior Analysis and Intervention (CASAS/HH)
April 25, 2023 updated by: Diane Cook, Washington State University
The world's population is aging and the resulting prevalence of chronic illnesses is a challenge that our society must address.
The vision is to address this challenge by designing smart environment technologies that keep older adults functioning independently in their own homes as long as possible.
Smart environments have been used as the basis of monitoring activities for residents with health conditions.
However, there is currently a lack of large scale, longitudinal research to identify early markers of dementia and other health status changes and to predict functional decline.
The objective of this project is to perform a 5-year longitudinal study of older adults performing daily activities in their own smart homes.
Study Overview
Status
Completed
Conditions
Detailed Description
By tracking residents' daily behavior over a long period of time our intelligent software can perform automated functional assessment and identify trends that are indicators of acute health changes and slower progressive decline (e.g., dementia).
By implementing prompt-based interventions that support functional independence and promote healthy lifestyle behaviors (e.g., social contact, exercise, regular sleep), the investigators can improve overall health and well-being.
The investigators hypothesize that smart home technologies can be used to detect and predict functional change, to slow functional change and extend functional independence, and to improve quality of life in elderly individuals who are at risk of transitioning to mild cognitive impairment and to dementia.
This hypothesis has been formulated on the basis of preliminary data produced by the applicants which supports the efficacy of using smart home technologies for both functional status assessment and for prompting the initiation and completion of activities in individuals with mild cognitive impairment and dementia.
The rationale of the proposed work is that understanding the natural history of functional change between aging and dementia will lead to early prevention and proactive interventions that will slow functional change, thereby delaying nursing home placement and cost of care to society.
The investigators plan to pursue the following specific aims: (1) Characterize the daily lifestyle of smart environment residents through minimal-supervision activity recognition and activity discovery, (2) Design software algorithms that detect trends in behavioral data, and (3) Evaluate the efficacy of activity-aware automated prompting technology for extending functional independence and improving quality of life.
The proposed work is innovative because it will track a large number of individuals longitudinal in their own homes and determine whether this technology can be used to promote healthy lifestyle behaviors and detect health care changes that may lead to early interventions, improved quality of life, and decreased health care utilization.
The project is significant because it will introduce new technologies for activity discovery and tracking that require minimal-supervision, contribute algorithms that predict cognitive decline and signal more acute health status change, and demonstrate for the first time that activity-aware automated prompting technologies can be used to support and/or slow functional change and to increase quality of life in elderly individuals.
Study Type
Observational
Enrollment (Actual)
44
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Washington
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Seattle, Washington, United States, 98101
- Horizon House
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Spokane, Washington, United States, 99223
- Moran Vista Senior Living
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Spokane, Washington, United States, 99223
- Rockwood Retirement Communities
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
75 years and older (Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Participants are older adults age 75+ who are currently living independently.
Description
Inclusion Criteria:
- fluent in English
- cognitively health adults and adults who meet criteria for Mild Cognitive Impairment (CDR score >= 0.5)
Exclusion Criteria:
- current or recent (past year) psychoactive substance abuse
- history of cerebrovascular accidents
- other known medical, neurological or psychiatric causes of cognitive dysfunction (Parkinson's schizophrenia, TBI)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Prompt intervention
The prompt intervention group will receive context-aware text, audio, and video prompts to initiate specified activities of daily living.
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No prompt intervention
The no prompt intervention will not receive any prompts to initiate activities of daily living.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in Clinical Dementia Rating
Time Frame: 24 months
|
Change in CDR score from baseline
|
24 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Change from Baseline in Amount of Caregiver Assistance
Time Frame: 24 months
|
24 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Diane Cook, PhD, Washington State University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2013
Primary Completion (Actual)
December 1, 2018
Study Completion (Actual)
December 1, 2018
Study Registration Dates
First Submitted
December 18, 2012
First Submitted That Met QC Criteria
January 30, 2013
First Posted (Estimate)
February 1, 2013
Study Record Updates
Last Update Posted (Actual)
April 27, 2023
Last Update Submitted That Met QC Criteria
April 25, 2023
Last Verified
April 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01EB015853-01A1 (U.S. NIH Grant/Contract)
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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