ReviewEpilepsy & behavior : E&B2016
Epilepsy misconceptions and stigma reduction: Current status in Western countries.
Review in Epilepsy & behavior : E&B, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 3 of them syntheses that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
32 citing papers in PubMed, 3 syntheses or guidelines pooled it, 105 citations in OpenAlex.
- Attitudes and misconceptions surrounding epilepsy and first aid of seizures in the Eastern Mediterranean Region: a systematic review and meta-analysis.BMC public health · 2026Pooled it
- Unfavorable public attitude toward people with epilepsy in Ethiopia: A systematic review and meta-analysis study.Epilepsia open · 2023Pooled it
- Epilepsy misconceptions and stigma reduction interventions in sub-Saharan Africa, a systematic review.Epilepsy & behavior : E&B · 2018Pooled it
- Clinical correlates of perceived stigma among people living with epilepsy enrolled in a self-management clinical trial.Epilepsy & behavior : E&B · 2024Trial
- A randomized prospective pilot trial of Web-delivered epilepsy stigma reduction communications in young adults.Epilepsia · 2017Trial
- Lived experiences that influence the quality of life among patients with epilepsy at Mulago National Referral Hospital.Epilepsy & behavior reports · 2026Article
- Epilepsy Knowledge, Attitudes, and First-Aid Practices Among Syrian University Students: A Cross-Sectional Study.Health science reports · 2026Article
- Article
- Stigma, overprotection, and suicidal ideation in epilepsy: a cross-sectional study on psychosocial predictors.Epilepsy & behavior reports · 2026Article
- Prior Knowledge of Epilepsy Predicts Positive Attitudes and Practices Toward Persons Living With Epilepsy.Brain and behavior · 2026Article
- The Effect of Fatalistic Tendency in Individuals on Attitudes Toward Epilepsy Patients.Brain and behavior · 2025Article
- Validation of the Japanese version of the scales of the attitudes toward people with epilepsy (SAPE-J).Epilepsia open · 2024Article
- Article
- Effects of stigma on the quality of life in patients with epilepsy.Acta epileptologica · 2024Article
- Epilepsy knowledge and attitudes: A large observational study among the Palestinian general public.Heliyon · 2024Article
- "The understanding and attitude toward epilepsy in the Souss-Massa region of Morocco".Epilepsia open · 2023Article
- Article
- Psychosocial Basis of Human Sufferings and Poverty in Patients with Neurological and Psychiatric Disorders.Medical research archives · 2023Article
- Article
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors at 5 institutions in 1 country.
Funding
Abstract
objectiveThis systematized literature review identified reports describing epilepsy misconceptions in the developed Western countries and research interventions focused on reducing these misconceptions. MATERIALS AND
methodsEnglish language publications from January 2004 to January 2015 that described original research conducted in Europe, North/Central/South America, or Australia on misconceptions about epilepsy among the general public were used for this review.
resultsEighty-one publications were selected. Most studies were conducted in the Americas (N=30) and Europe (N=31). Misconceptions and attitudes about epilepsy were assessed among clinical providers (N=9), family members of people with epilepsy (PWE) (N=5), teachers (N=11), students (N=22), and the general public (N=25). Most studies used structured questionnaires, sometimes adding open-ended questions. Misconceptions reflected socially exclusionary attitudes directed at PWE, ignorance about treatment, and overgeneralizations that are stigmatizing when applied to all PWE. Misconceptions were more prevalent in those with less education, lower socioeconomic status, and no exposure to PWE. There were only 12 intervention studies. While intervention studies were generally effective in improving attitudes, many were targeted to healthcare and education settings, were time-intensive, and impractical for broad general population implementation. None incorporated newer technology-based strategies regarding effective health communication approaches.
conclusionsTypes of epilepsy misconceptions were similar in reports published over the last decade, although most referred to misconceptions that have already been previously described. Existing questionnaires may fail to identify more subtle forms of current misconceptions and negative attitudes. Few interventional studies specifically target epilepsy stigma. Practical and broad scalable approaches to destigmatize epilepsy may help reduce misconceptions.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.