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临床试验/NCT03517592
NCT03517592Unknown不适用

A Multicenter Phase II Rater-Blinded Randomized Controlled Trial to Compare the Effectiveness of Eye Movement Desensitization Reprocessing Therapy vs. Treatment as Usual in Patients With Substance Use Disorder and History of Psychological Trauma

Parc de Salut Mar4 个研究点 分布在 1 个国家目标入组 142 人开始时间: 2018年9月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
142
试验地点
4
主要终点
Reduction in severity of consumption

研究概览

简要总结

The main objective of this project is to test whether EMDR therapy is effective in reducing substance use and improving clinical and trauma-related symptoms in SUD patients with a history of psychological trauma.

详细描述

Background:

Substance use disorders (SUD) represent an important social and public health problem due to their negative consequences in terms of delinquency, family disintegration, academic and occupational disengagement, mental illness, transmission of infectious diseases, intoxication and mortality rates. As with other mental disorders, the evolution of this disorder depends on many biological and sociodemographic variables, such as the age of onset of consumption, access to drugs, one's living environment, race, and the presence of stressors. Of all these variables, adverse events are being increasingly investigated, due to the strong negative impact they have on the onset, course and prognosis of psychiatric disorders, especially when psychological trauma is present. Traumatic events, especially in childhood or adolescence, are considered to be a robust risk factor for developing post-traumatic stress disorder (PTSD), with or without further comorbid severe mental disorders such as depression, bipolar disorder, psychosis or SUD. A recent meta-analysis published in the Lancet found multiple adverse childhood events to be a significant risk factor for problematic alcohol and substance use, highlighting the impact of adverse childhood events even when not associated with a diagnosis of PTSD. Although there is currently no available data about the prevalence of traumatic events in SUD patients population, it is estimated that is likely high presumed to be high. The results of different studies estimate that the prevalence of PTSD in inpatients with SUD to ranges from 25% -51%, which is two to four times higher than the prevalence range found in the general population (1.3% -12.3%). In addition, evidence suggests that PTSD and traumatic events are correlated with addiction severity, with a worse disease prognosis, with a greater number of hospitalizations, with a poorer response to treatment, with shorter periods of abstinence and with greater craving. Thus, an integral model with an individualized treatment plan is indicated in SUD, including psychological trauma as a specific objective to address.

A possible candidate for this is Eye Movement Desensitization and Reprocessing (EMDR) therapy, which is considered to be a first line treatment for PTSD, being recommended by different international bodies, such as the American Psychiatric Association (APA) and World Health Organization (WHO). EMDR is a psychotherapeutic approach designed to alleviate the distress associated with traumatic memories, facilitating the access to and processing of traumatic memories and other adverse life experiences and bringing these to an adaptive resolution using standardized protocols and elements of cognitive behavioral, interpersonal, and body-centered therapies in conjunction with bilateral stimulation (e.g. horizontal eye movements from side to side). In recent years, the use of EMDR has increased exponentially in clinical practice due its effectiveness and safety and that has resulted in investigations in additional populations beyond PTSD, such as in those with depression, anxiety, chronic pain, bipolar disorder, or psychosis. Of note, three small randomized controlled trials (RCT) of EMDR versus Treatment As Usual (TAU) have also been performed in patients with SUD. The results suggest that EMDR, compared to the control group, significantly improved craving, depression, anxiety, self-esteem and dissociative symptoms, but samples were small. A large scale RCT is currently underway, which aims to determine the efficacy of EMDR in reducing PTSD symptoms in an inpatient sample with comorbid PTSD or subthreshold PTSD and SUD. In view of the above, we consider that a further large RCT of EMDR in the treatment of psychological trauma in outpatients with SUD, including psychological trauma related to adverse events not covered by DSM-V diagnostic criteria, is crucial and clinically necessary due to the negative impact it has on the course and prognosis of these illnesses, and in order to confirm or reject prior first positive evidence. Our study is also important in including patients with dual pathology and measuring impact on psychopathological symptoms, which will help facilitate the application of EMDR in a real world setting if it is shown to be efficacious.

Design:

This is a single-blind RCT with two parallel branches, EMDR and TAU, in patients diagnosed with SUD who have suffered from comorbid psychological trauma. The patients will be matched by center, age, sex and diagnosis. One group will consist of TAU + 20 individual EMDR sessions, 60 minutes each, during 6 months, the other group will receive TAU only. Patients will be evaluated at baseline, at 3 months, post-treatment at 6 months and at 12 months as follow-up.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age between 18 and 65 years
  • outpatients
  • presence of one or more traumatic events, which causes currently trauma associated symptoms (Scale of the impact of the event-reviewed, IES-R> 0) and subjective Disability Unit (SUD)>5)

排除标准

  • presence of organic brain diseases
  • presence of suicidal ideas
  • having received a trauma focused therapy in the last 2 years

结局指标

主要结局

Reduction in severity of consumption

时间窗: Changes from baseline to visits at 3, 6 and 12 months.

To measure changes in the Severity of Dependence Scale. 4-point Likert scale (0 - 3). The higher score indicate greater dependence.

Reduction of general psychopathological symptoms associated with psychiatric comorbidity

时间窗: Change from baseline to visits at 6 and 12 months.

To measure changes in the Brief Psychiatric Rating Scale. It ranges from 18 to 126: the higher the score, the worse the general psychopathology symptoms.

Reduction in the number of relapses

时间窗: Change of relapses from baseline to visits at 3, 6 and 12 months.

To measure relapses with the Timeline Followback Questionnaire. It is a retrospective calendar-based measure of daily substance use.

Reduction in level of consumption

时间窗: Changes from baseline to visits at 3, 6 and 12 months.

To measure changes in the Visual Analog Scale. It ranges from 0 to 10: the higher the score, the greater the craving severity.

Reduction in depressive symptoms associated with a comorbid psychiatric disorder

时间窗: Changes from baseline to visits at 6 and 12 months.

To measure changes in the Hamilton Depression Rating Scale. Total scores range from 0 to 52: the higher the score, the worse the depressive symptoms.

Reduction of (hypo) manic symptoms associated with a comorbid psychiatric disorder

时间窗: Changes from baseline to visits at 6 and 12 months.

To measure changes in the Young Mania Rating Scale. It ranges from 0 to 130: the higher the score, the worse the manic symptoms.

次要结局

  • Detection of Childhood life traumatic events(Childhood. It is administered only during the baseline visit.)
  • Making a PTSD diagnosis(Changes from baseline to visits at 6 and 12 months.)
  • Improvement of global functioning(Changes from baseline to visits at 6 and 12 months.)
  • Detection of traumatic events in the last year(The last year. It is administered only during the baseline visit.)
  • Assessment of the severity of trauma-related symptoms.(The previous 7 days. Changes from baseline to visits at 6 and 12 months.)
  • Detection of dissociative symptoms(Changes from baseline to visits at 6 and 12 months.)

研究者

发起方
Parc de Salut Mar
申办方类型
Other
责任方
Sponsor

研究点 (4)

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