Studies have revealed that ERA is a common phenomenon with a prevalence rate ranging from 29% - 75% (
14). Due to negative attitudes and misconceptions, most of the patients experience a feeling of fear and anxiety. On the other hand, studies have shown that the patients, after treatment, do not find it a really frightening and painful experience (
15). Our study supported this finding because ERA was significantly lower among the patients with a history of ECT. Notably, a majority of the participants (92.3%) appeared to have ERA. According to the findings of this survey, the main cause of ERA was GA and memory impairment, followed by electrical current. We found out that different ERA levels and causes have been reported by similar studies. Rajogopal et al. reported that one third of their cases had had fear and anxiety of ECT due to their inadequate information (
16). The other studies indicated that a high-quality informed consent could help the patients suffer from less anxiety. In Vergese’s et al. study, the proportion of patients with ERA was 75%, and the main cause of such an anxiety was memory disturbance (
17). In Hughes’ et al. study, 44% of the patients experienced anxiety before ECT mostly due to their fear of memory loss (
18). Guruvaiah et al. reported severe fear and anxiety in 17% of their participants before ECT. They found the patients had higher levels of anxiety for GA than ECT. This finding was in a similar vein with our findings. Malcolm et al. reported that 60% of the patients had some levels of fear and anxiety before ECT, and the most common reasons for such a feeling were brain damage and memory loss, followed by GA and pain (
19). In Gallinek’s et al. study, 67% of the cases experienced ERA before the treatment (
20). Comparing our findings with the other findings, in spite of the similarity regarding the causes of fear and anxiety, a larger number of patients reported ERA in this study. Definitely, we have to focus on these findings and pay enough attention to find out the underlying problems such as the role of social media. We noticed that GA was the most common cause of ERA, while it has been confirmed that ECT under GA was a revolution that brought safety to the procedure. Accordingly, it seems that enough time has not been devoted to provide the patients with accurate and real information. In general, the differences among the studies with regard to the wide range of ERA prevalence could be explained by different methodologies. Firstly, there was no agreement on a standard definition for ERA. Secondly, there were different measurement scales for anxiety, including researcher-developed questionnaires or researcher-developed interviews, whose validity and reliability are not confirmed. Thirdly, the non-heterogeneous populations were included in the studies. Unlike some previous studies, our participants were not candidates for ECT therapy. They were hospitalized in psychiatric ward and they were on medication. They were included in this study because they had better views and communication skills to answer the questions. In addition, although they were not receiving ECT courses, they were exactly the patients who might require them due to their resistant conditions, their own request, or any other unexpected emergency situation. Moreover, cultural differences, beliefs, and levels of education should also be taken into consideration. Another effective factor was the interview time. Obviously, the results might be different when the patients are interviewed retrospectively, compared to the cases interviewed before the treatment. Studies have shown that longer intervals are associated with higher levels of ERA. The effects of forgetting should be considered, which was not included according to the methodology of this study. The potential effects of forgetting on the results was disregarded. Additionally, we did not specify different levels of ERA. Obviously, 92.3% of the participants with ERA were not in the same condition. For example, Guruvaiah et al. reported severe fear and anxiety in 17% of their participants. Our results might be different if we limit ERA to the severe forms. To sum up, according to our findings, further attempts should be made to plan effective strategies to eliminate ERA in patients. In this regard, a well-developed informed consent form, which provide enough information to the patients and their families, could be as the first effective measure.