LifeBio Memory Digital Reminiscence Platform
- Conditions
- DementiaCognitive Impairment
- Interventions
- Other: LifeBio Memory
- Registration Number
- NCT04769466
- Lead Sponsor
- Benjamin Rose Institute on Aging
- Brief Summary
Non-pharmacological interventions and person-centered care strategies are important elements of care for people with Alzheimer's disease and related dementias. Life story work, which uses written and oral life histories to elicit conversation and memories, is an effective intervention for individuals with dementia; however, because of the time-consuming nature of generating useful life story materials, has not been widely implemented in nursing homes and other care environments. LifeBio Inc. will develop an easy-to-use reminiscence therapy platform - LifeBio MemoryTM - with a novel machine-learning-based application that converts speech to text and generates life stories to serve as an interactive tool to cultivate communication between people living with dementia and their family and caregivers.
- Detailed Description
This project offers the unique and timely opportunity to evaluate the feasibility, acceptability, and efficacy of LifeBio Memory's effectiveness as a solution for improving quality of life and quality of care for older adults in long-term care settings, as well as relationships with staff caregivers. This project will implement the the newly developed LifeBio Memory platform and train caregivers in X sites across the state of Ohio, with X residents and X staff participating in a feasibility trial. The program will be evaluated using three waves of data collection from staff during training and throughout implementation, as well as pre-post resident data to evaluate the effectiveness of the new intervention.
The LifeBio Memory platform addresses the need for an intuitive, artificial intelligence-driven solution to the traditionally labor-intensive process of collecting, sharing, and celebrating the life stories of older adults, as well as the development of tools for staff caregivers to enhance person-centered care practices and care-planning. It has great potential for improving psychosocial outcomes for participants, enhancing relationships between care staff and residents, and a cost-effective way to identify ways in which life stories can be used to provide a foundation for preference-based, personalized care.
Residents will be interviewed at baseline, then again at follow-up (4 weeks later), staff members being trained to utilize the LifeBio Memory application and provide feedback on the materials, as well as completed a survey at baseline, again at follow-up
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 160
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Residents LifeBio Memory Residents will be screened for their cognitive status and compete interviews with a researcher prior to participation in the life story interview. Residents will then be interviewed again at T3 about four weeks after the life story books, summaries, and staff materials have been delivered. Staff LifeBio Memory Staff will be trained in the platform, and complete life story interviews with residents at their facilities. Upon completion of training, staff will complete surveys regarding it's effectiveness and utility, and following the completion of the interview, the resident's life story books, summary materials, and staff tools will be delivered four weeks later. Life story materials are meant to assist staff in providing more personalized care and a mechanism for residents to feel more deeply understood.
- Primary Outcome Measures
Name Time Method Change in Resident Satisfaction with Care [Modified version of the Ohio Nursing Home Resident Satisfaction Survey] from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Measurement of care satisfaction; Scale: 1 (generally yes) to 2 (generally no)
Change in Person-Centered Care Assessment Tool [Sub-Scales I and II] from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Measurement of staff experience with person-centered care in their current care community; Scale: 0 (strongly agree) to 4 (strongly disagree)
Change in Direct Care Worker Job Satisfaction Scale from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Measurement of staff satisfaction with different aspects of their job; Scale: 0 (very dissatisfied) to 3 (very satisfied)
Adherence to LifeBio Memory Treatment Protocol After intervention (4 weeks from baseline) Items related to staff adherence to LifeBio Memory program protocols
Change in Satisfaction with Care in the Nursing Home Scale from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Measurement of resident satisfaction with care in a long-term care facility
Change in Center for Epidemiological Studies Depression Scale (CES-D) from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Measure of depressive symptomatology; Scale: 0 (rarely or none of the time) to 3 (most or almost all of the time)
Change in Quality of Life Alzheimer's Disease (QoL-AD) from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Quality of life for an individual living with Alzheimer's Disease: Scale: 1 (poor) to 4 (excellent)
Change in Cohen-Mansfield Agitation Inventory (CMAI) - Short Form from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Measurement of agitation; Scale: 1 (never) to 7 (several times an hour)
Change in Attitudes towards Residents Scale from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Measurement of the attitudes of staff long term care staff towards the residents under their care
Change in Individualized Care Instrument (ICI) from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Measurement of care recipient perceptions of individualized nursing care; Scale: 1 (strongly disagree) to 4 (strongly agree)
Change in The UCLA 3-Item Loneliness Scale from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Measurement of feelings of loneliness; Scale: 0 (hardly ever) to 2 (often)
Change in Perceived Usefulness of LifeBio Memory from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Items related to staff perceived usefulness of the LifeBio Memory program
Satisfaction with LifeBio Memory After intervention (4 weeks from baseline) Items related to overall satisfaction with the LifeBio Memory program
Change in Sense of Competence in Dementia Care Staff (SCIDS) Scale from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Measurement of sense of dementia care competence; Scale: 0 (very much) to 3 (not at all)
- Secondary Outcome Measures
Name Time Method Change in Mini Mental Status Examination (MMSE) from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Screening for resident cognitive status
Change in Adequate Knowledge of Care Preferences from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Items related to staff knowledge of resident care preferences
Change in Understanding of Resident's Life Story from Baseline Baseline, pre-intervention; After intervention (4 weeks from baseline) Items related to staff understanding of resident life stories
Length of Life Story Interview After intervention (4 weeks from baseline) Items related to the amount of time spent doing the life story interview
Trial Locations
- Locations (1)
Benjamin Rose Institute on Aging
šŗšøCleveland, Ohio, United States