Epilepsy Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults between 18 and 60 years old who have been diagnosed with epilepsy and whose epilepsy specialist has confirmed them as a suitable candidate for surgery
- People who are able to give their own consent to participate without assistance
- People who are fluent in English
- People whose reading level is at or above an 8th grade standard, as measured by a specific reading test (the WRAT-4)
- People who have access to the internet and are able to participate in online video streaming
- People who have not previously had brain surgery to remove or destroy brain tissue, though prior use of nerve stimulation devices (such as RNS, VNS, or DBS) is acceptable
- People who are willing and able to take part in a program aimed at improving thinking and memory skills
Who may not be able to join:
- People who have taken part in any kind of cognitive (thinking or memory) rehabilitation or training program within the last 6 months
- People who are involved in an ongoing legal case related to the cause of their epilepsy, unless that legal matter is only about a disability application (short- or long-term)
- People currently undergoing intensive treatment for a serious or life-threatening illness, such as chemotherapy, that could affect their ability to participate
- People with a serious psychiatric condition that could interfere with participation, such as schizophrenia, active psychosis, active mania, or current thoughts of suicide
- People with significant hearing or vision loss that would prevent participation in remote cognitive testing or the cognitive training program
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Kayela Arrotta, PhD, The Cleveland Clinic
Phone: 216-444-6101
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Intervention attendance; Rate of Homework Completion; Study Attrition; Intervention Efficacy based on Quality of Life
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.