RESUMO
Objective: The current multi-university, multi-disaster study examined the impact of natural disaster exposure on identity-related distress through life stressors and posttraumatic stress symptoms (PTSS). Participants: Young adult university students (n = 665, 77% female, M = 20.5 years old) participated in Wave (W) 1. Half provided contact information for follow-up, and 136 university students participated in W2. Method: University students in the mainland U.S. and Puerto Rico were asked about disaster exposure, life stressors, PTSS, and identity-related distress at W1 (M = 9.7 months post-disaster) and identity-related distress at W2 (M = 12.4 months after W1). Two serial mediation models assessed the indirect effect of disaster exposure on W1 and W2 identity-related distress through life stressors and PTSS. Results: Disaster exposure impacted identity-related distress concurrently and longitudinally through increasing life stressors since disaster and PTSS. Conclusion: Potential supportive services should address identity-related distress among disaster-exposed young adults with PTSS.
RESUMO
Community-Based Participatory Research promotes the inclusion of diverse voices in the research process and in decision-making processes. However, there are very few research studies that collaborate with children, especially within the context of schools. Promoting child participation has benefits both for children as well as for schools. Nonetheless, this may depend on how adults react to such participation. The present study is part of a broader study on school violence prevention. Our objective is to explore school personnel's concept of childhood and how it relates to their opinions about child school participation. We conducted a discussion group with nineteen (19) faculty and non-faculty members of a public school to ask them questions about the topic. We categorized participants' answers and analyzed relationships among them. Results suggest that participants' concept of childhood is linked to socio-cultural and historical factors and that it impacts their opinions about child participation. Also, school personnel recognize that child participation has benefits for children, the school and the wider society. This contrasts with deficiencies on how to articulate this participation beyond traditional classroom strategies. We discuss the implications of these results for pedagogical practice and for participatory research as promoters of children voices in context.
RESUMO
El proceso de estigmatización asume una devaluación de la persona debido a una característica o marca que haya sido identificada socialmente y que permita que se le describa como diferente. Desde que se desató la epidemia del VIH/SIDA, vivir con la enfermedad ha sido señalado de manera social como una marca estigmatizante. Las manifestaciones de dicha estigmatización se han documentado entre profesionales de la salud. Este estigma puede afectar los servicios de salud que las personas que viven con VIH/SIDA reciben de estos profesionales. Los objetivos de esta investigación fueron explorar: 1) la percepción que tienen estudiantes y profesionales de la salud sobre su nivel de competencia para ofrecer servicios a personas que viven con VIH/SIDA, 2) las opiniones de éstos sobre el tipo de adiestramiento profesional recibido y la necesidad del mismo, y 3) la manifestación de actitudes estigmatizantes como indicadores de necesidad de adiestramiento profesional. La muestra total del estudio estuvo compuesta por 80 de diversas profesiones de la salud. Los resultados reflejan que algunos/as de los/as participantes han recibido formación en VIH pero ésta no ha sido suficiente para contrarrestar las nociones estigmatizantes. Discutimos las implicaciones de los resultados para investigaciones futuras y el desarrollo de intervenciones con vías de minimizar las nociones estigmatizantes en los escenarios de salud
Stigma is defined as the devaluation of a person due to the possession of a characteristics that has negative social meanings. Since the onset of the HIV/AIDS epidemic, living with HIV entails a social stigma. These manifestations are particularly dangerous since they might entail lack of service for people who live with HIV/AIDS (PLWHA). This study has as its goals to explore: (a) the perceived level of competence of students and health professionals for delivering services to PWLHA, (b) their opinions regarding their completed and needed training, and (c) the existence of stigmatising attitudes towards PLWHA. The sample includes 80 participants (40 students and 40 professionals) from the fields of medicine, nursing, psychology and social work. Results evidence that participants have received training in HIV but these did not address important social issues such as myths, fears, and stigma. Implications to future research and for the development of interventions to address stigma in health scenarios is discussed (AU)
