Computerized Cognitive Training in Epilepsy
- Conditions
- Epilepsy
- Registration Number
- NCT02726191
- Lead Sponsor
- NYU Langone Health
- Brief Summary
The purpose of this randomized uncontrolled single-site trial is to evaluate the efficacy of two novel computerized cognitive enhancing software packages for improving cognitive and behavioral outcomes in patients with epilepsy.
- Detailed Description
The proposed investigation will be the first to pit two software packages against each other to evaluate the relative efficacy and feasibility of their use among patients with epilepsy. Pharmacotherapy fails to control seizures in approximately 30% of patients. Use of non-pharmacologic interventions, such as cognitive rehabilitation, has shown some benefit for improving cognitive functions and reducing mood symptoms. Each of the computer exercises employ a set of stimuli that are generalizable and mimic real-world experiences.
Recruitment & Eligibility
- Status
- WITHDRAWN
- Sex
- All
- Target Recruitment
- Not specified
- Documented diagnosis of epilepsy based on medical records. The records will be reviewed by the PI and the approved study personnel to confirm that a diagnosis of epilepsy has been made.
- Must own a computer or have access to the internet.
- Full Scale IQ < 80, as assessed by the WASI-II.
- History of chronic progressive neurologic or neurodegenerative illnesses (e.g., Parkinson's disease, multiple sclerosis, dementia, primary or metastatic malignancy). Patients with headache or migraine are not excluded.
- History of Axis I psychiatric illness with psychotic features. (e.g., schizophrenia). Patients with depression or anxiety (treated or untreated) without psychotic features are not excluded.
- Visual or auditory impairment, which precludes participation in part, or all of the testing.
- English as a first language will not be required, but participants must have either received some of their schooling in English or used English in their work for >10 years.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Total Index Score from the Repeatable Battery for the Assessment of Neurocognitive Status (RBANS) 8 Weeks
- Secondary Outcome Measures
Name Time Method The Everyday Cognition Scale (ECog) 8 Weeks Perceived cognitive abilities on an index of subjective cognitive abilities (Cognitive Self-Report Questionnaire; CSRQ-25) 8 Weeks Measure of mood (Geriatric Depression Scale) 8 Weeks
Trial Locations
- Locations (1)
New York University School of Medicine
🇺🇸New York, New York, United States
New York University School of Medicine🇺🇸New York, New York, United States