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巴黎 MEM 研究方案:2015-2016 年法国恐怖袭击后创伤后应激障碍治疗的有效性和效率试验研究方案。

Paris MEM: a study protocol for an effectiveness and efficiency trial on the treatment of traumatic stress in France after the 2015-16 terrorist attacks.

机构信息

Département de Psychiatrie adulte, boulevard de l'Hôpital, 75013, Paris, France.

Department of Psychiatry, McGill University, Montréal, Canada.

出版信息

BMC Psychiatry. 2019 Nov 8;19(1):351. doi: 10.1186/s12888-019-2283-4.

Abstract

BACKGROUND

The Paris and Nice terrorist attacks affected a thousand of trauma victims and first-line responders. Because there were concerns that this might represent the first of several attacks, there was a need to quickly enhance the local capacities to treat a large number of individuals suffering from trauma-related disorders. Since Reconsolidation Therapy (RT) is brief, relatively easy to learn, well tolerated and effective, it appeared as the ideal first-line treatment to teach to clinicians in this context.

METHODS

This study protocol is a two-arm non-randomized, multicenter controlled trial, comparing RT to treatment as usual for the treatment of trauma-related disorders. RT consists of actively recalling one's traumatic event under the influence of the ß-blocker propranolol, once a week, for 10-25 min with a therapist, over 6 consecutive weeks. This protocol evaluates the feasibility, effectiveness, and cost-utility of implementing RT as part of a large multi-center (N = 400) pragmatic trial with a one-year follow-up.

DISCUSSION

Paris MEM is the largest trial to date assessing the efficiency of RT in the aftermath of a large-scale man-made disaster. RT could possibly reinforce the therapeutic arsenal for the treatment of patients suffering from trauma-related disorders, not only for communities in western countries but also worldwide for terror- or disaster-stricken communities.

TRIAL REGISTRATION

Clinical Trials (ClinicalTrials.gov). June 3, 2016. NCT02789982.

摘要

背景

巴黎和尼斯恐怖袭击影响了上千名创伤受害者和一线救援人员。由于担心这可能是多次袭击中的第一次,因此需要迅速增强当地治疗大量创伤相关障碍患者的能力。由于再巩固治疗(RT)简短、相对容易学习、耐受性好且有效,因此它似乎是在这种情况下教授临床医生的理想一线治疗方法。

方法

本研究方案是一项两臂非随机、多中心对照试验,比较 RT 与常规治疗治疗创伤相关障碍。RT 包括在β受体阻滞剂普萘洛尔的影响下每周主动回忆一次创伤事件,每周一次,每次 10-25 分钟,由治疗师在 6 周内连续进行。该方案评估了在为期一年的随访中,作为一项大型多中心(N=400)实用试验的一部分实施 RT 的可行性、有效性和成本效益。

讨论

巴黎 MEM 是迄今为止评估 RT 在大规模人为灾难后效率的最大试验。RT 可能会增强治疗创伤相关障碍患者的治疗武器库,不仅适用于西方国家的社区,也适用于遭受恐怖袭击或灾难的全球社区。

试验注册

临床试验(ClinicalTrials.gov)。2016 年 6 月 3 日。NCT02789982。

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