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Impact of Neuropsychological Evaluation on Epilepsy Treatment

University of South Florida logo

University of South Florida

Status and phase

Unknown
Phase 2

Conditions

Epilepsy

Treatments

Behavioral: Neuropsychological testing

Study type

Interventional

Funder types

Other

Identifiers

NCT03202082
Satisfaction after Evaluation

Details and patient eligibility

About

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.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 89 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

100 participants in 2 patient groups

Neuropsychological testing
Experimental group
Description:
Participants from this group will be administered a neuropsychological battery in addition to the initial and follow-up surveys
Treatment:
Behavioral: Neuropsychological testing
Treatment as usual
No Intervention group
Description:
Participants from this group will be administered the initial and follow-up survey.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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