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Behavioral Intervention
Experimental Group for Alzheimer's Disease (FL-REACH Trial)
N/A
Waitlist Available
Research Sponsored by University of Central Florida
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
1. Age 18-89 2. Identified caregiver or care partner of an individual who has been diagnosed with Alzheimer's disease or another dementia by the memory disorders clinic, and/or who has sought ongoing treatment through the memory disorders clinic 3. Able to provide informed consent 4. Able to engage in the intervention weekly by attending sessions in person at the clinic 5. Able to participate in the intervention in English or in Spanish 6. No previous experience with a caregiver training program in the past (this applies to theory based, structured interventions delivered by professionals, and does not include peer-led support groups that the family may have engaged with)
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, session 2, 4, 6 (therapy termination); 6 month follow-up
Awards & highlights
FL-REACH Trial Summary
This study is evaluating whether a modified version of the REACH II intervention can be implemented in an outpatient clinic.
Eligible Conditions
- Alzheimer's Disease
- Dementia
FL-REACH Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowFL-REACH Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, session 2, 4, 6 (therapy termination); 6 month follow-up
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, session 2, 4, 6 (therapy termination); 6 month follow-up
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Alzheimer's disease Knowledge Scale
Caregiver Burden
Preparedness for Caregiving Measure
Secondary outcome measures
FL-REACH Satisfaction Survey
Health Self-Report
Risk Assessment
FL-REACH Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Experimental GroupExperimental Treatment1 Intervention
Participants will complete the FL-REACH annualized caregiver intervention.
Group II: Control GroupActive Control1 Intervention
No-intervention control group
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Who is running the clinical trial?
AdventHealthOTHER
106 Previous Clinical Trials
29,498 Total Patients Enrolled
University of Central FloridaLead Sponsor
78 Previous Clinical Trials
1,097,437 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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