Actively Recruiting
I-CARE 2: Mobile Telehealth to Reduce Alzheimer'S-related Symptoms
Led by Indiana University · Updated on 2025-11-24
184
Participants Needed
2
Research Sites
217 weeks
Total Duration
On this page
Sponsors
I
Indiana University
Lead Sponsor
N
National Institute on Aging (NIA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study is a randomized, controlled trial (RCT) to evaluate the effect of Brain CareNotes (a mobile health application) on the burden experienced by unpaid caregivers of patients with dementia and on the behavioral and psychological symptoms of dementia (BPSD) displayed by care recipients. Over 39 months, the trial will enroll 184 caregivers of community-dwelling patients diagnosed with Alzheimer's disease or a related dementia (ADRD). Caregivers will be randomized to use the Brain CareNotes app or an attention control education-only app for 12 months, with usage reminders.
CONDITIONS
Official Title
I-CARE 2: Mobile Telehealth to Reduce Alzheimer'S-related Symptoms
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Self-identified primary unpaid caregiver of a person diagnosed with Alzheimer's disease or related dementia (ADRD) at any stage who is receiving primary care and living in the community
- Able to read and understand English
- Age 18 years or older
You will not qualify if you...
- Care recipient is a permanent resident of an extended care facility (nursing home)
- Participation in another clinical trial that would interfere with this study's objectives
- Sensory or other impairment that prevents use of a mobile touchscreen device or other study activities, even after correction
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
IU Health
Indianapolis, Indiana, United States, 46202
Actively Recruiting
2
Community Health Network
Indianapolis, Indiana, United States, 46203
Actively Recruiting
Research Team
M
Miriam J Rodriguez, PhD
CONTACT
J
Jordan R Hill, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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