Actively Recruiting
Cognitive Enhancement Intervention for Creating a Healthy L.I.F.E (Lifestyle Interventions for Epilepsy)
Led by Kayela Arrotta · Updated on 2025-07-03
170
Participants Needed
1
Research Sites
140 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to test if cognitive interventions in those with diagnosed epilepsy can help lessen cognitive lapses and improve overall brain health. Participants will participate in weekly, virtual group sessions led by a neuropsychologist for 12 weeks. After the 12-week mark, participants will be asked to practice what they learned for 9 more months. Participants will be asked to complete online questionnaires at certain times during the study. Researchers will compare this intervention group to another group that did not get the intervention to see if the intervention improves brain health. Participation in each of these groups will be randomly assigned. Participation in the study will last for one year.
CONDITIONS
Official Title
Cognitive Enhancement Intervention for Creating a Healthy L.I.F.E (Lifestyle Interventions for Epilepsy)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 to 60 years with diagnosed epilepsy
- Subjective cognitive difficulties or objective cognitive deficits
- Able to provide informed consent independently
- Fluent in English
- Reading skills at or above 8th grade level
- Access to internet and ability to participate in online video streaming
- No history of epilepsy surgery
- Willing and able to take part in cognitive intervention
You will not qualify if you...
- Diagnosis of non-epileptic or psychogenic seizures
- Cognitive rehabilitation/intervention within last 6 months
- Enrolled in another interventional epilepsy study at enrollment
- Planned epilepsy surgery within 6 months
- Pending litigation related to epilepsy cause unless for disability application
- Undergoing intensive treatment for serious illness affecting participation
- Serious psychiatric conditions interfering with participation
- Currently pregnant or less than 6 weeks postpartum
- Significant hearing or vision loss preventing remote testing or intervention
- Requires legal authorized representative or lacks capacity to consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cleveland Clinic
Cleveland, Ohio, United States, 44195
Actively Recruiting
Research Team
A
Anthony Lioi, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here