Epilepsy Epilepsy
Conditions
Interventions
Patients are randomized into two treatment arms: the standard care arm and the
ultra-fast AI arm. In the ultra-fast AI arm, an ambulant EEG recording is
performed and analyzed by an artificial intel
Sponsors
Medisch Spectrum Twente (MST)
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: - The participant must be an adult (>=18 years). - The participant is referred for a routine EEG with the differential diagnosis of epilepsy.
Exclusion criteria
Exclusion criteria: - Patients with cognitive impairments that limits patients* understanding of the research purpose and to give informed consent. - Patients who previously have been diagnosed with epilepsy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameter is the time-to-diagnosis, defined as the time (in weeks) from initial referral to final diagnosis of epilepsy. | — |
Secondary
| Measure | Time frame |
|---|---|
| - Total cost of each study arm. - Time spend by medical professionals reviewing the EEGs. - Sensitivity, specificity and F1 score of routine EEG and ambulatory EEG with AI. - Patient satisfaction score measured by the patient satisfaction questionnaire. - Time patients invested in the diagnostic process of both study arms. | — |
Countries
Netherlands
Contacts
Public ContactE.C. Klaver
Medisch Spectrum Twente (MST)
Outcome results
None listed