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Mobile Application of Seizure Diary (Brain4U) in Epilepsy Care

Mobile Application of Seizure Diary (Brain4U) in Epilepsy for the Better Patient Care

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04023851
Enrollment
119
Registered
2019-07-18
Start date
2019-04-12
Completion date
2020-07-15
Last updated
2020-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epilepsy

Keywords

Epilepsy, Seizure diary, Mobile application

Brief summary

The study is intended to evaluate the impact of mobile application on management and knowledge acquisition in patients with epilepsy.

Detailed description

Investigators assess the general and personal knowledge of epilepsy, compliance of antiepileptic drugs (AED), and self efficacy scale. Participants be asked to use the mobile application (Brain4U) and record seizure type, frequency of seizures, aggravating factors, and adverse events related to antiepileptic drugs for 2 month period.

Interventions

DEVICEMobile application Brain4U

Brain4U application provides participants to record seizures, medications, side effects, and combined psychiatric problems. It also reminds participants when to take antiepileptic drugs.

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Participants must be between the ages of 1-99. * Participants must attend Seoul National University Bundang Hospital Pediatric Neurology Outpatient Clinic. * Participants under age 18 must have an adult guardian give informed consent. * Participants must have a functioning smartphone (iOS or Android) which can download the and perform Brain4U application. * Participants must be able to use mobile application skillfully.

Exclusion criteria

* Person who does not have smartphone nor restricted to use mobile application can not participate this study. * Person with intellectual disability or unable to use mobile application can not participate this study.

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of knowledge acquisition in epilepsy2 monthsBaseline and 2 month Timepoint scores from questionnaires are assessed. Improvement in knowledge acquisition and self-efficacy by using questionnaire. 1. Genetal knowledge (G) Questionnaire: There are total 10 questions (1 point score for each question) to evaluate general knowlege about epilepsy. Score reported as (mean, SD), higher scores are better. Score ranges 0 to 10. 2. Persional knowledge (P) questionnaire: There are total 4 questions (1 point score for each question) to evaluate knowlege about individual's epilepsy. Score reported as (mean, SD), higher scores are better. Score ranges 0 to 4. 3. Self-efficacy scale (SE): There are 4 questions (1 point score for each question) to evaluate self-efficacy scale. Score reported as (mean, SD), higher scores are better. Score ranges 0 to 4.

Secondary

MeasureTime frameDescription
AED compliance2 monthsBaseline and 2 month Timepoint AED compliances are reported. Assess improvement of AED compliance by comparing Days with AED per month before and after using mobile application. Count the Days with AED in a month and converted to the percentage. Percentage ranges 0 to 100%. The high percentage means good compliance which means less AED skipping in a month.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026