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Behavioral Intervention
Fully Asynchronous Online Savvy Program for Dementia
N/A
Waitlist Available
Led By Fayron Epps, PhD, RN
Research Sponsored by Emory University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, month 2, month 3
Awards & highlights
Study Summary
This study is evaluating whether a psychoeducation program can help caregivers of people with dementia.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, month 2, month 3
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, month 2, month 3
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Caregiver Mastery Scale Score
Change in Center for Epidemiologic Studies - Depression (CES-D) Score
Change in Revised Memory and Behavior Problem Checklist (RMBPC) Frequency Score
+3 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Fully Asynchronous Online Savvy ProgramExperimental Treatment1 Intervention
Family caregivers of PLWD taking part in a fully asynchronous online caregiver education program.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Fully Asynchronous Online Savvy Program
2021
N/A
~60
Find a Location
Who is running the clinical trial?
National Institute on Aging (NIA)NIH
1,665 Previous Clinical Trials
28,005,019 Total Patients Enrolled
265 Trials studying Dementia
23,623,351 Patients Enrolled for Dementia
Emory UniversityLead Sponsor
1,636 Previous Clinical Trials
2,560,570 Total Patients Enrolled
20 Trials studying Dementia
2,776 Patients Enrolled for Dementia
Fayron Epps, PhD, RNPrincipal InvestigatorEmory University
4 Previous Clinical Trials
307 Total Patients Enrolled
2 Trials studying Dementia
92 Patients Enrolled for Dementia
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