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Behavioral and Environmental Sensing and Intervention

Behavioral and Environmental Sensing and Intervention for Dementia Caregiver Empowerment

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03297268
Acronym
BESI
Enrollment
24
Registered
2017-09-29
Start date
2016-05-31
Completion date
2019-08-31
Last updated
2017-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavioral and Psychiatric Symptoms of Dementia, Caregivers, Dementia

Keywords

Dementia Caregiver Empowerment, Caregiver Burden, Agitation in Dementia, Environmental Sensors, Wearable Technology

Brief summary

This 3-phase research plan to employ Behavioral and Environmental Sensing and Intervention (BESI) will overcome the fundamental scientific barriers to realizing prediction of agitation episodes and detection early stages of dementia related agitation. The goal of which is empowering caregivers to intervene early and ultimately reduce agitation, thus reducing caregiver burden and extending aging-in-place and improving the associated quality-of-life and cost benefits.

Detailed description

The dementia syndrome of Alzheimer's disease and other disorders is rapidly expanding due to the aging of society and the longevity of citizens. In its varying stages, care of the dementia syndrome requires differing sets of skills from the caregivers, and more skilled intervention is required as the disease progresses. These caregivers experience increased burden due to the challenges and stresses of caring. A recent systematic review of caregiver burden factors revealed dementia-related agitation to be the most prevalent factor leading caregivers to institutionalize community-dwelling loved ones with dementia. Tools that empower caregivers to proactively reduce the incidents and severity of agitation would reduce stress and increase self-efficacy, thereby extending aging-in-place and the associated quality-of-life and cost benefits. This project proposes to develop, deploy, and evaluate such a tool and to address the fundamental scientific challenges to realizing the benefits of such a technology to caregivers and persons with dementia (PWD). The tool - BESI: Behavioral and Environmental Sensing and Intervention - will be an empowerment tool for caregivers of community-dwelling PWD. BESI comprises: 1. a system of body-worn inertial sensors and in-home acoustic, light, temperature, and motion sensors, 2. data analysis techniques to detect and assess agitation and environmental context from these sensor streams, 3. models for the relationship between agitation and the environment that are trained for each PWD-caregiver dyad based on a&b, and 4. automated real-time notifications to the caregiver based on b&c (e.g., detection of early agitation stages or of an environment (cumulative and/or instantaneous based on the models) that has led to agitation in the past), empowering the caregiver to intervene before agitation escalation.

Interventions

OTHERIntervention with Home-Based Caregivers

We will assess whether real-time notifications of potential agitation via a wearable wrist device improves caregiver self-efficacy.

Sponsors

Carilion Clinic
CollaboratorOTHER
North Carolina Agriculture & Technical State University
CollaboratorOTHER
University of Virginia
Lead SponsorOTHER

Study design

Observational model
FAMILY_BASED
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of dementia * Living in one home for at least 2 months without hospitalization * Caregiver seeking support for caregiving needs * Have a stable caregiver * Be able to provide consent or assent

Exclusion criteria

* Hospitalization in the last 2 months * Multiple and inconsistent caregivers * Living in multiple homes * Unable to provide consent or assent * No known dementia

Design outcomes

Primary

MeasureTime frameDescription
Improved Caregiver Self-Efficacy30 daysIncreased scores on Revised Scale for Caregiver Self-Efficacy
Decreased Caregiver Burden30 daysZarit Burden Interview score lowered

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026