Can a low-cost eye-tracker assess the impact of a valent stimulus? A study replicating the visual backward masking paradigm

Capturing affective response to valent stimuli using eye-tracking is not only of interest to academic research, but also to commercial equipment developers (e.g., car dashboards). In order to investigate whether a low-cost eye-tracker can effectively detect participants’ physiological response to negatively valent stimuli, forty-four participants aged 19-24 (mean = 24.7, SD = 5.8) were recruited to complete the visual backward masking paradigm in a repeated-measures experimental design. Saccadic duration and pupil sizes were recorded using a lower-end 60-hz tracker. Data was analysed using a mix of parametric and non-parametric tests. Our results suggest that valence in the form of fearful vs neutral faces has a significant main effect on both saccadic duration [V = 931, p < 0.001, d = 0.96] and pupil size [t(43) = 29.81, p < 0.001, d = 3.91)]. Our findings were further supported by Bayes Factor analysis, which showed that saccadic duration data was 24 times more likely to occur, and pupil size measurement data was 89 times more likely, under the alternative hypothesis, showing that differences in valence had a main effect. The combined evidence produced by our Bayesian analysis, the large effect sizes of our frequentist analysis, and the significant effect on two separate measurements lead us to suggest that, under the right conditions, low-cost eye trackers can successfully detect changes in saccadic duration and pupil sizes as a result of physiological responses to threat-relevant visual stimuli

The Psychological Burden of Families with Diabetic Children: A Literature Review Focusing on Quality of Life and Stress

Chronic diseases, such as childhood diabetes mellitus (DM), are a complex and continuous struggle as well as a great challenge both for the children who face the disease and for their parents. DM is characterized by the complex management of therapeutic treatments, thus causing physical and psychological complications infamily members. There are many families who, upon hearing the diagnosis of their child with DM, stand still in front of these new facts as their lives change. All these unprecedented conditions cause parents intense stress and discomfort, leading them to a mental burden, as the only thing that concerns them upon diagnosis is how the family will survive in the face of the current conditions they are experiencing as well as the future of the sick child. The purpose of this brief literature review is to present the research findings related to the psychological burden of families withchildren with DM, focusing on the quality of life and stress

Genotoxic and Antigenotoxic Assessment of Chios Mastic Oil by the In Vitro Micronucleus Test on Human Lymphocytes and the In Vivo Wing Somatic Test on Drosophila

International audienceChios mastic oil (CMO), the essential oil derived from Pistacia lentiscus (L.) var. chia (Duham), has generated considerable interest because of its antimicrobial, anticancer, antioxidant and other beneficial properties. In the present study, the potential genotoxic activity of CMO as well as its antigenotoxic properties against the mutagenic agent mitomycin-C (MMC) were evaluated by employing the in vitro Cytokinesis Block MicroNucleus (CBMN) assay and the in vivo Somatic Mutation And Recombination Test (SMART). In the in vitro experiments, lymphocytes were treated with 0.01, 0.05 and 0.10% (v/v) of CMO with or without 0.05 μg/ml MMC, while in the in vivo assay Drosophila larvae were fed with 0.05, 0.10, 0.50 and 1.00% (v/v) of CMO with or without 2.50 μg/ml MMC. CMO did not significantly increase the frequency of micronuclei (MN) or total wing spots, indicating lack of mutagenic or recombinogenic activity. However, the in vitro analysis suggested cytotoxic activity of CMO. The simultaneous administration of MMC with CMO did not alter considerably the frequencies of MMC-induced MN and wing spots showing that CMO doesn't exert antigenotoxic or antirecombinogenic action. Therefore, CMO could be considered as a safe product in terms of genotoxic potential. Even though it could not afford any protection against DNA damage, at least under our experimental conditions, its cytotoxic potential could be of interest