Psychosocial Burden of Epilepsy
Perceived Stigma, and Social Misconceptions in People With Epilepsy
1 other identifier
observational
90
1 country
1
Brief Summary
This study aims to investigate the educational, occupational, and social challenges experienced by individuals with epilepsy using structured questionnaires developed by the research team. Despite advances in diagnosis and treatment, people with epilepsy may continue to face difficulties related to stigma, access to opportunities, and daily functioning. Participants will complete survey forms designed to assess barriers encountered in school, workplace, and social environments, as well as their perceptions and experiences related to living with epilepsy. The findings are expected to provide insight into unmet needs and inform strategies to improve support and quality of life for individuals with epilepsy.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Feb 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2026
CompletedFirst Submitted
Initial submission to the registry
February 26, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2026
CompletedFirst Posted
Study publicly available on registry
March 4, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2026
CompletedApril 30, 2026
February 1, 2026
28 days
February 26, 2026
April 24, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Educational, occupational, and social difficulties
The proportion and severity of self-reported difficulties experienced by individuals with epilepsy in educational settings, workplace participation, and social life, as measured by structured survey forms designed by the research team.
At study enrollment (single assessment)
Eligibility Criteria
Adults with a clinical diagnosis of epilepsy who are under follow-up at a tertiary neurology clinic will be invited to participate. The study population consists of individuals receiving routine clinical care who are able to complete structured questionnaires assessing educational, occupational, and social experiences related to living with epilepsy. Participants are expected to represent a broad range of demographic and clinical characteristics reflective of real-world epilepsy care.
You may qualify if:
- Adults aged 18 years or older
- Clinical diagnosis of epilepsy confirmed by a neurologist
- Able to understand and complete the questionnaire
- Willing to provide informed consent
You may not qualify if:
- Severe cognitive impairment preventing reliable questionnaire completion
- Acute medical or psychiatric condition interfering with participation
- Inability to communicate effectively in the study language
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Saglik Bilimleri University Izmir Faculty of Medicine Department of Neurology
Izmir, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 26, 2026
First Posted
March 4, 2026
Study Start
February 1, 2026
Primary Completion
March 1, 2026
Study Completion
April 1, 2026
Last Updated
April 30, 2026
Record last verified: 2026-02