| Grant number: | 14/04810-0 |
| Support Opportunities: | Regular Research Grants |
| Start date: | August 01, 2014 |
| End date: | July 31, 2017 |
| Field of knowledge: | Health Sciences - Medicine - Psychiatry |
| Principal Investigator: | Felipe D Alessandro Ferreira Corchs |
| Grantee: | Felipe D Alessandro Ferreira Corchs |
| Host Institution: | Instituto de Psiquiatria Doutor Antonio Carlos Pacheco e Silva (IPq). Hospital das Clínicas da Faculdade de Medicina da USP (HCFMUSP). Secretaria da Saúde (São Paulo - Estado). São Paulo , SP, Brazil |
| City of the host institution: | São Paulo |
| Associated researchers: | Alvaro Cabral Araujo ; Clarice Gorenstein ; Eduardo Wagner Aratangy ; Francisco Lotufo Neto ; Joana Singer Vermes |
Abstract
Posttraumatic Stress Disorder (PTSD) has been understood as failure to get over traumatic memories or to extinguish conditioned responses related to traumatic events. Current behavioral treatments, such as Prolonged Exposure (PE), aim to promote such processes, however, high rates of relapse and the existence of refractory cases demand new strategies. One line of research has gained special attention in this sense: the one that disrupt the reconsolidation of memories. In the present study, three experiments intend to explore it. In "Experiment 1", recent trauma victims will be randomized to receive PE: 1- within the traumatic retrieval window, or 2- without prior traumatic retrieval. It is expected that group 1 will have less responses to traumatic memory retrieval in future tests. In "Experiment 2", subjects with severe and refractory PTSD will be randomly assigned to receive Electroconvulsive Therapy (ECT) in one of the 2 groups described in "Experiment 1", in order to assess whether the technique applied after retrieval would cause greater disruption to the traumatic memory. In "Experiment 3", a laboratory model of fear will be applied in subjects who are receiving ECT for clinical reasons. Patients will be randomly assigned to get an ECT session in one of the two models described in Experiments 1 and 2. It is expected that the results can increase the knowledge about new forms of treatment and prevention of PTSD. (AU)
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