Assessment of the Knowledge among Caregivers of Epileptic Patients Regarding Epilepsy

Abstract

Aim: Epilepsy is a spectrum of disorders with range of severities, widely differing seizure types and causes, an array of coexisting conditions and varying impacts on patients and families. Living with epilepsy patients exposes one to challenges at home, school, workplace, and other outdoor places. Awareness and understanding of epilepsy nature are, hence, critical to create a better attitude among family caregivers to provide a better care for the patients as well as improve their health-related quality of life.

Methodology: The present study based on the quantitative approach. A research design selected for the present study was non-experimental exploratory design. Using non-probability purposive sampling 200 caregivers of epileptic patients were selected. The tool used for the data collection was semi-structured questionnaires. Pilot study was conducted from November 5, 2019 to November 13, 2019 in selected hospitals. After explaining the study purpose, objectives, role participants, benefits to the participant, and then a written consent was taken from subjects. Knowledge was assessed with the help of semi-structured questionnaire. Collected data were arranged properly and analyzed as per the objectives of the study.

Results: The result of the study shows that 23.5% of the caregivers have poor knowledge score (0–09), 50% of caregivers have average knowledge score (10–18) and (26.5%) of the caregivers have good knowledge score (19–26).

Conclusion: Demographic variable, educational status, and age were found to have significant association with the knowledge score.