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首页> 外文期刊>American journal of orthopsychiatry >Feasibility, Preliminary Efficacy, and Safety of a Randomized Clinical Trial for Asian Women's Action for Resilience and Empowerment (AWARE) Intervention
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Feasibility, Preliminary Efficacy, and Safety of a Randomized Clinical Trial for Asian Women's Action for Resilience and Empowerment (AWARE) Intervention

机译:随机临床试验的可行性,初步疗效和安全性亚洲妇女的弹性和赋权(意识)干预

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To our knowledge, Asian Women's Action for Resilience and Empowerment (AWARE) is the first gender-and culture-specific and trauma-informed group psychotherapy intervention designed for Asian-American young women with histories of interpersonal violence and trauma and/or Post-Traumatic Stress Disorder (PTSD) diagnosis. We employed a 2-arm randomized controlled trial. Sixty-three women who met clinical criteria for trauma were randomized to the intervention (n = 32) or waitlist control (n = 31) group. We documented retention rates, preliminary efficacy for sexual risk behaviors and depressive symptoms (overall and stratified by PTSD at baseline), and safety in terms of suicidality at baseline, postintervention, and 3-month follow-up. AWARE demonstrated high retention rates, in that 87.50% of those enrolled in the program completed at least 6 out of the 8 sessions. Although there were no differences overall for sexual risk behaviors or depressive symptoms, among women with PTSD, significant reductions in depressive symptoms were observed in treatment compared to control, with an effect size of.84. Suicidal ideation and intent were reduced in both the treatment and control groups, with no attempts during the trial. AWARE is uniquely tailored to serve a pressing clinical need. These results support its feasibility and safety. A large-scale trial targeted at women with PTSD is recommended to further explore the efficacy of AWARE.
机译:据我们所知,亚洲妇女的恢复力和赋权(意识)是第一个针对亚裔美国少妇的第一个针对人际暴力和创伤和/或创伤后创伤后历史应激障碍(PTSD)诊断。我们雇用了2臂随机对照试验。六十三名符合创伤临床标准的妇女被随机分配到干预(n = 32)或候补人员控制(n = 31)组。我们记录了保留率,性风险行为和抑郁症状的初步疗效(通过基线的PTSD整体和分层),以及在基线的自由性方面的安全性和3个月随访。意识到展示了高保留率,在该计划中注册的87.50%的人员至少完成了8个会议中的至少6个。虽然性风险行为总体上没有差异,但在接触者的妇女中,与对照相比,在治疗中观察到抑郁症状的显着减少,其效果大小为84。在治疗和对照组中,在治疗和对照组中减少了自杀式念头和意图,在试验期间没有尝试。意识到唯一定制,以提供紧迫的临床需求。这些结果支持其可行性和安全性。建议在具有应税专神经禁妇女的大规模试验,以进一步探索意识的效果。

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