Tackling the global problem of traumatic stress in low-income countries: a pilot clinical trial comparing reconsolidation therapy to paroxetine in Nepal.
Autor: | Brunet A; Research Centre of the Douglas Mental Health University Institute, and Department of Psychiatry, McGill University, 6875 boulevard LaSalle, Montréal, Quebec, H4H 1R3, Canada. alain.brunet@mcgill.ca., Sapkota RP; Research Centre of the Douglas Mental Health University Institute, and Department of Psychiatry, McGill University, 6875 boulevard LaSalle, Montréal, Quebec, H4H 1R3, Canada.; Division of Social and Transcultural Psychiatry, Global Mental Health Program, McGill University, Montréal, QC, Canada., Guragain B; Centre for Victims of Torture (CVICT), Kathmandu, Nepal., Tremblay J; Research Centre of the Douglas Mental Health University Institute, and Department of Psychiatry, McGill University, 6875 boulevard LaSalle, Montréal, Quebec, H4H 1R3, Canada., Saumier D; Research Centre of the Douglas Mental Health University Institute, and Department of Psychiatry, McGill University, 6875 boulevard LaSalle, Montréal, Quebec, H4H 1R3, Canada., Kirmayer LJ; Division of Social and Transcultural Psychiatry, Global Mental Health Program, McGill University, Montréal, QC, Canada.; Culture and Mental Health Research Unit, Lady Davis Institute, Jewish General Hospital, Montréal, QC, Canada. |
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Jazyk: | angličtina |
Zdroj: | BMC psychiatry [BMC Psychiatry] 2021 Sep 03; Vol. 21 (1), pp. 434. Date of Electronic Publication: 2021 Sep 03. |
DOI: | 10.1186/s12888-021-03441-6 |
Abstrakt: | Background: Traumatic stress is a global mental health problem requiring novel, easily implemented treatment solutions. We compared the effectiveness and efficiency of Reconsolidation Therapy (RT) to the well-established antidepressant paroxetine, in reducing symptoms of traumatic stress among patients from Nepal, a low-income country. Methods: Forty-six adults with posttraumatic stress disorder (PTSD) were randomized to one of two groups. The reconsolidation blocker propranolol was administered 90 min before briefly recalling a traumatic memory with a therapist, weekly for six consecutive weeks. This was compared to daily paroxetine for 26 weeks. Self-reported PTSD symptoms were assessed blindly at the 7th, 13th, and 26th weeks. Results: An intent-to-treat analysis revealed a robust pre- to post-treatment main effect (β Conclusion: RT also displayed promising efficiency, considering that it had been discontinued weeks earlier while the paroxetine treatment was continued, as recommended. RT could be taught in low-income countries as part of the local therapeutic resources to treat the core symptoms of PTSD, provided that such results are replicated on a broader scale. Trial Registration: ISRCTN34308454 (11/10/2017). (© 2021. The Author(s).) |
Databáze: | MEDLINE |
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