NCT05888610CompletedNot Applicable
Identifying Specifications for Caregiver-assisted Solutions to Assess Dementia Patient Needs at Home
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Prepped Health LLC
- Enrollment
- 10
- Locations
- 2
- Primary Endpoint
- Number of Days that Participants Use Digital Outpost
Study Overview
Brief Summary
The goal of this clinical trial is to test a mobile application amongst caregiver's supporting patients diagnosed with Alzheimer's Disease and Related Dementias (ADRD). The main question it aims to answer is: Will caregivers supporting patients diagnosed with ADRD utilize a mobile application to routinely report symptoms of the patients they care for?
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Supportive Care
- Masking
- None
Eligibility Criteria
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Caregiver of a Duke patient with Alzheimer's disease or Alzheimer's disease-related dementias (ADRD), participating in the Duke Dementia Family Support Program
- •The ability to speak and understand English
- •Age > 18 years
Exclusion Criteria
- •Those unable to speak and understand English
- •Age ≤ 18 years
Outcomes
Primary Outcomes
Number of Days that Participants Use Digital Outpost
Time Frame: Time Frame up to week 2
Completion of at least 75% of Digital Outpost across 4 days within a 2-week period
Number of Clinical Assessments Completed
Time Frame: Time Frame up to week 2
Completion of at least 75% of Clinical Assessments
Secondary Outcomes
- Usability as Measured by the System Usability Scale at 2 weeks(Time Frame 2 weeks)
Investigators
Study Sites (2)
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