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Randomized Controlled Trial: Provision of EMDR Protocol for Recent Critical Incidents and Ongoing Traumatic Stress to First Responders

机译:随机对照试验:为最近的关键事件提供EMDR协议,并对第一响应者进行创伤性压力

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This randomized controlled trial aimed to evaluate the effectiveness of the Eye Movement Desensitization and Reprocessing Protocol for Recent Critical Incidents and Ongoing Traumatic Stress (EMDR-PRECI) in reducing posttraumatic stress disorder (PTSD), anxiety, and depression symptoms related to the work of first responders on active duty. Participants were randomly assigned to two 60-minute individual treatment sessions (N = 30) or to a no-treatment control condition (N = 30). They completed pre-, post-, and follow-up measurements using the Posttraumatic Stress Disorder Checklist for Diagnostic and Statistical Manual of Mental Disorders, fifth edition {DSM-5) (PCL-5) and the Hospital Anxiety and Depression Scale (HADS). Data analysis by repeated measures analysis of variance (ANOVA) showed clear effects of the EMDR-PRECI in reducing PTSD work-related symptoms in the treatment group with symptom reduction maintained at 90-day follow-up with a large effect size (d = 3.99), while participants continued to experience direct exposure to potentially traumatic work-related events during the follow-up period. Data analysis by repeated measures ANOVA revealed a significant interaction between time and group, F (2,116) = 153.83, p < .001, iotp~2 = .726 for PTSD, and for anxiety F (1,58) = 37.40, p < .005, iotP2 = .090, but not for depression. A t-test showed a clear decrease for depression symptoms for the treatment group with statistically significant results. The study results suggest that the EMDR-PRECI could be an efficient and effective way to address first responders' work-related PTSD, anxiety and depression symptoms. Future research is recommended to replicate these results and to investigate if symptom improvement also results in the reduction of physical health symptoms and early retirement for PTSD-related reasons among first responders.
机译:这种随机对照试验旨在评估眼球运动脱敏和再处理方案的有效性,用于降低与首次工作的失血性应激障碍(PTSD),焦虑和抑郁症状(PTSING),焦虑和抑郁症状的持续创伤应激(EMDR-PREPI)。积极职责的响应者。将参与者随机分配到两个60分钟的单个治疗会话(n = 30)或无治疗控制条件(n = 30)。他们使用精神障碍的诊断和统计手册,第五版{DSM-5)(PCL-5)和医院焦虑和抑郁症(HAFS)完成了预先改造和统计手册的前后和后续测量。 。通过重复措施的差异分析(ANOVA)的数据分析表明,EMDR-Preci在减少治疗组中的治疗组中有关的症状的明显效果,其症状减少维持在90天随访,效果大小(D = 3.99 ),虽然参与者在随访期间继续在潜在的创伤工作相关事件中进行直接暴露。通过重复测量的数据分析Anova在PTSD中揭示了时间和组之间的显着相互作用,F(2,116)= 153.83,P <.001,IOTP〜2 = .726,以及焦虑F(1,58)= 37.40,P < .005,IOTP2 = .090,但不是抑郁症。 T检验表明,治疗组的抑郁症状明显减少,具有统计学上显着的结果。该研究结果表明,EMDR-Preci可能是一个有效而有效的方法,可以解决第一个受访者与工作相关的应激障碍,焦虑和抑郁症状。建议将来的研究复制这些结果并调查症状改善是否导致在第一个响应者之间减少身体健康症状和早期退休的接触相关原因。

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