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Cognitive Training for Cognitive Impairment (EFIT Trial)
N/A
Waitlist Available
Research Sponsored by Clemson University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, immediate post-test at 14 weeks, and 3 month follow-up at 26 weeks
Awards & highlights
EFIT Trial Summary
The Everyday Function Intervention Trial
Eligible Conditions
- Cognitive Impairment
- Dementia
- Healthy Aging
EFIT Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, immediate post-test at 14 weeks, and 3 month follow-up at 26 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, immediate post-test at 14 weeks, and 3 month follow-up at 26 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change from Baseline Daily Everyday Cognitive Assessment (DECA) at 14 and 26 weeks
Change from Baseline Useful Field of View (UFOV) test at 14 and 26 weeks
Change from Baseline iFunction at 14 and 26 weeks
Secondary outcome measures
Change from Baseline Objective sleep at 14 weeks
EFIT Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Cognitive TrainingExperimental Treatment1 Intervention
20 hours of computerized brain exercises
Group II: Cognitively Stimulating ActivitiesActive Control1 Intervention
20 hours of computerized brain exercises
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Cognitive Training
2008
Completed Phase 3
~4100
Find a Location
Who is running the clinical trial?
Clemson UniversityLead Sponsor
33 Previous Clinical Trials
5,797 Total Patients Enrolled
National Institute on Aging (NIA)NIH
1,668 Previous Clinical Trials
28,004,968 Total Patients Enrolled
Frequently Asked Questions
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