Impact of Neuropsychological Evaluation on Epilepsy Treatment

Phase 2

• Conditions: Epilepsy
• Interventions: Behavioral: Neuropsychological testing

• Registration Number: NCT03202082
• Lead Sponsor: University of South Florida

Brief Summary

The present study aims to expand the evidence base of neuropsychological services in the context of medical management of epilepsy, examining whether treatment outcome and patient satisfaction with medical care are significantly improved when neuropsychological evaluation is included as an additional component of medical care within a comprehensive epilepsy center. All participants will complete an initial survey and a follow-up survey regarding views towards their epilepsy treatment. Participants will be randomized into one of two groups. One group will be given a neuropsychological battery in addition to the survey. The primary study hypothesis is that the addition of neuropsychological services to treatment-as-usual will result in significant improvements in (a) satisfaction with medical care, (b) patient perceived treatment outcome, and (c) physician-rated medical compliance. The secondary hypothesis is that participants who undergo neuropsychological evaluation will be generally satisfied with their experience with neuropsychological services.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-07-01
• Status Verified: 2017-06
• Study First Submitted: 2017-06-26
• Study First Submitted QC: 2017-06-26
• Last Update Submitted: 2017-06-26
• Study First Posted: 2017-06-28
• Last Update Posted: 2017-06-28
• Primary Completion: 2018-06-30
• Study Completion: 2018-06-30

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

• 18 years of age or older
• experiencing some degree of epilepsy-related symptoms, but not of such severity as to preclude them from being able to provide consent or undergo neuropsychological assessment (requiring extended inpatient treatment, severely aphasic, or MMSE score < 25)

Exclusion Criteria

• Previously undergone neuropsychological testing
• Currently pursuing surgical treatment for epilepsy

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Neuropsychological testing	Neuropsychological testing	Participants from this group will be administered a neuropsychological battery in addition to the initial and follow-up surveys

Primary Outcome Measures

Name	Time	Method
Epilepsy Outcome Study Survey	2-4 months	A brief questionnaire regarding the participants views on their epilepsy treatment

Trial Locations

Locations (1)

University of South Florida; 🇺🇸 Tampa, Florida, United States