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Evaluating the Efficacy of a Mobile Epilepsy Education Application

Anxiety | Epilepsy | Knowledge, Attitudes, Practice | Epilepsy in Children

Background. Following a childhood diagnosis of epilepsy, children and their families encounter significant concerns about the disease trajectory, side effects of anti-seizure medications, and long-term prognosis. The multitude of uncertainties can cause significant anxiety in the family, often within the context of limited supports and resources. Epilepsy education can help address these concerns, mitigating the development of anxiety, ultimately leading to better patient-, family- and system-level outcomes. Globally, the MEEP is the only mobile application providing education, monitoring of symptoms, and tracking of medical appointments. The original MEEP was developed, tested, and integrated into practice in Turkey; the investigators will now evaluate the efficacy of an English and French version of the MEEP for families of children with epilepsy in Canada.

A two-group, single-center, randomized controlled intervention trial with 1:1 allocation ratio will be conducted in the Pediatric Neurology Clinic of the Montreal Children's Hospital. Seventy-two caregivers of children with epilepsy (intervention=36, control= 36), aged 1-17 years and treated at the study site will be eligible. Family Introduction Form, Epilepsy Information Scale for Parents and Parental Anxiety Scale for Seizures will be used to collect data at baseline and 3 weeks post-delivery of the 7-week intervention. The MEEP consists of 2 parts. The first part entails the delivery of the educational content of the MEEP, and the second part consists of a "Parental Monitoring Section." Comparator. The control group will continue to benefit from the standard educational services provided by the study site.

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    0 and up

Critères de participation

Inclusion Criteria:

* Parents/caregivers whose children are between 1-17 years old;
* Parents/caregivers whose child was diagnosed with epilepsy at least 2 months ago;
* At least one primary caregiver is comfortable interacting in English or French; and
* At least one primary caregiver owns and uses a smartphone on a daily basis.

Exclusion Criteria:

- Inability to provide informed consent for any reason.

Lieu de l'étude

Montreal Children's Hospital
Montreal Children's Hospital
Montréal, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Saoussen Berrahmoune, PhD

[email protected]
514-934-1934
Research Institute of the McGill University Health Centre
Research Institute of the McGill University Health Centre
Montréal, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Dr. Kenneth Myers, MD

[email protected]
514-934-1934
Backup Contact

Saoussen Berrahmoune, PhD

[email protected]
Étude parrainée par
McGill University Health Centre/Research Institute of the McGill University Health Centre
Participants recherchés
Plus d'informations
ID de l'étude: NCT06402526