Elderly Chronic Diseases Online Biometric Analysis Home Living Technology
NCT ID: NCT02155686
Last Updated: 2019-01-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
536 participants
INTERVENTIONAL
2014-08-27
2019-01-01
Brief Summary
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This project aims to demonstrate that home automation and telemonitoring can lead to develop a home safety environment that could help the elderly and individual with disability live independently in their own home.
In this study, the automation sensors containing devices follow up chronic disease clinical factors to monitor their biometrical parameters and detect any abnormal prodromal disease decompensation via telemonitoring and geriatric expertise.
The purpose of this study is:
* to provide clinical evidence of the effectiveness of automation tools and telemonitoring/expertise for the home support for people at risk of loss of autonomy
* to demonstrate the clinical benefit of combining the automation and telemonitoring and geriatric teleexpertise
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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Biosensors
Participants in this arm are equipped both with home telecare/automation and with biometric sensors
Biosensors
Device: Biometric sensors; Home automation; telecare
Home automation
Automation
Participants in this arm are equiepd with home automation only
Home automation
Interventions
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Biosensors
Device: Biometric sensors; Home automation; telecare
Home automation
Eligibility Criteria
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Inclusion Criteria
* House equipped with home automation
* Having been hospitalized in the year prior to the inclusion for the following conditions : heart failure, chronic obstructive pulmonary disease (COPD ), diabetes, high blood pressure ( hypertension ) , repetitive falls, chronic renal failure , stroke, neurodegenerative diseases , malnutrition (according to criteria HAS)
* Multiple chronic diseases (at least 2 comorbidities) .
* Having given free and informed consent
Exclusion Criteria
* Enrolled in another clinical trial
65 Years
ALL
No
Sponsors
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University Hospital, Limoges
OTHER
Responsible Party
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Principal Investigators
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Thierry DANTOINE, MD
Role: STUDY_CHAIR
CHU Limoges
Locations
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Service de Gériatrie - CHU de LImoges
Limoges, , France
Countries
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Other Identifiers
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I13027
Identifier Type: -
Identifier Source: org_study_id
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