To explain the low employment rates of people with disabilities (PwDs), emerging debates have revealed an unexploited potential impact of assistive technology (AT) on human talent and the inclusion process. This article provides a systematic review to critically evaluate the current trends in the literature on AT. A systematic review was performed according to the inclusion criteria of the PRISMA-S guidelines, followed by a thematic analysis identifying the main themes by which the literature on the subject is organized. Finally, the Human Activity Assistive Technology (HAAT) model was used to deepen the contents taken into consideration in the scientific literature and to discuss the concept of workplace inclusion and its use. Forty-one studies fully met the eligibility criteria of the systematic review. The thematic analysis produced four clusters related to the impact and characteristics of AT in the workplace. Overall, the use of the HAAT model highlighted a lack of studies on the affective and socio-cultural dimensions that characterize the use of AT in the workplace. It is concluded that the deployment of AT can and should work on multiple levels to shape the workplace experiences of PwDs.

Background: Despite the growing interest in addiction research, which demonstrates the potential predictive role of adverse childhood experiences (ACEs), little is known about their impact on the psychological symptoms of craving. Methods: After reviewing the relevant diagnostic criteria for addiction and comorbid mental disorders along with routinely collected clinical and service-use data, 208 outpatients were assessed on the study protocol. Following the recruitment phase, nominal and ordinal data were analyzed using nonparametric methods. Results: Most of the outpatients reported ACEs (89.1%) and experienced cravings (73.4–95.7%). A positive association between ACEs and either intention and preplanning (r = .14, p < .05) or lack of control (r = .15; p < .05) of the craving behavior was found. Conclusion: Craving behavior in addiction remains a subject of debate. Although correlation analyses showed significant associations between reported ACEs and measures of craving, they were relatively small.

In the aftermath of the SARS-CoV-2 pandemic, and in due course for a full recovery to reduce the health burden and complications of the disease, the public discussion has moved from a pandemic slowdown to a more monitoring-based approach in public health. Stay-at-home rules, quarantine requirements for the infected ones, along with local lockdowns and social distancing measures around the planet have shown how vulnerable could be the ties between one’s demographic origins, morbidity and mortality.

Background:Caregiving for individuals with neurological disease involves providing physical, emotional, and social support, which can be a challenging and stressful experience. This study aims to compare the caregivers' burden, including the impact on mental and physical health, social support, and quality of life, in different neurodegenerative disorders. Methods:Fifty-five primary caregivers (F=41;mean age=53.07±12.29) of patients with Parkinson's Disease (PD=26), Multiple System Atrophy (MSA=16), and Amyotrophic Lateral Sclerosis (ALS=13), took part in the study. Standardized screening scales for the quality of life (EQ-5D/EQ-VAS and PQoL), levels of the caregiving burden (CBI and FSQ), and the assessment of the anxiety-depressive axis (HADS) were administered. Results: The mean CBI score was higher for caregivers of MSA patients (28.81±21.90) and ALS (25.15±16.23) than for caregivers of PD patients (16.08±10.34; p=0.036). Critical burden (cut-off>36) was present in the caregivers of MSA (31.3%), ALS (23.1%), and PD (19.2%) patients. Caregivers of patients with ALS had a worse perception of quality of life (EQ-5D total score) than caregivers of patients with MSA and PD (p

The impact of restrictions on movement resulting from the SARS-CoV-2 pandemic may contribute to a disruption of mental health in young people during this era. In March 2021, lockdown restrictions were enforcing national policies of tackling the infectious disease across the globe. In the early stages of the vaccination rollout, public enquires on confidence to endure the virus pandemic have shown high levels of psychological distress. Under the above circumstances, 333 university students were asked to fill in an online-based survey on alcohol consumption, compulsive behavior as a loss of control over eating, fear of weight changes, excessive sleepiness and sleep deprivation. Text mining and multiple correspondence analysis were employed to analyze qualitative data on the lived experience against the occurrence of health-related behaviors. Data analyses have showed that the pandemic was associated with a mixed breakup of clustered lemmas based on sex, age, and relationship status. The extent to which the participants have reported a lower degree of satisfaction on living arrangements, intimate and family relationships were interpreted as meaningfully related with a more negative lived experience. Social confinement has resulted as an immediate action for mitigating a public health crisis from the SARS-CoV-2 disease. Incidentally, social measures to mitigate the virus transmission have sought to protect internal collapse of the health care systems by reducing the number of casualties. Conversely, these findings provide new evidence on the social determinants of health among youth and consequently highlight the potential interference from missing social interactions in the COVID-19 pandemic response.