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临床试验/NCT05923697
NCT05923697Unknown不适用

The Feasibility and Potential Efficacy of Adding Addiction-focused EMDR to Regular Addiction Treatment A Multiple Baseline Study in Inpatients Who Use Non-opioid Drugs

IrisZorg2 个研究点 分布在 1 个国家目标入组 9 人开始时间: 2023年11月6日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
9
试验地点
2
主要终点
Therapist acceptability

研究概览

简要总结

Rationale: It is well established that Substance Use Disorders (SUD) have severe health consequences. Despite behavioral and pharmacological treatment options, relapse rates remain high. In particular, for non-opioid drugs, such as amphetamines, cocaine, base-coke and cannabis, established, evidence-based pharmacological options to reduce craving, to substitute substance use or to enforce abstinence are lacking. Therefore, there is a need for effective interventions for patients who use non-opioid drugs to reach and maintain long-term abstinence.

A potential interesting intervention is addiction-focused Eye Movement Desensitization and Reprocessing (AF-EMDR) therapy. However, the limited research on AF-EMDR therapy and mixed findings thus far prohibit clinical use. Recently, on the basis of diverse findings thus far, an adjusted AF-EMDR therapy protocol has been developed.

详细描述

Objective: to investigate areas of uncertainty about a possible future pilot RCT using AF-EMDR as an add-on intervention in inpatients who use non-opioid drugs and receive regular, inpatient addiction treatment, by determining:

  • Feasibility.
  • Potential clinical efficacy.

Study population: adults with a primary non-opioid use disorder, who are admitted to an inpatient addiction care clinic. A total of nine eligible participants will be allocated (allocation ratio 1:1:1) at random, in a non-concurrent fashion to one of three baseline durations.

Intervention: a total of four 90 min. sessions of AF-EMDR twice per week added to TAU.

Main study parameters/endpoints:

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • In order to be eligible to participate in this study, patients must meet the following criteria:
  • Diagnosis of Tobacco Use Disorder according to the DSM-5 (American Psychiatric Association, 2013) criteria.
  • Age ≥ 18 years.
  • Good Dutch language proficiency (based on clinical judgement).
  • Smoking, on average, ≥ 10 cigarettes per day pre-admission.
  • A score of at least 5 on a scale from 0 to 10, for motivation and self-efficacy
  • A planned inpatient stay of ≥ 4 weeks.
  • Written informed consent.

排除标准

  • A patient who meets any of the following criteria will be excluded from participation in this study:
  • Serious therapy interfering behavior or symptoms that also interfere with TAU, based on clinical judgement (e. g. psychiatric or medical crisis that requires immediate intervention).

结局指标

主要结局

Therapist acceptability

时间窗: 1 year

The acceptability of AF-EMDR to therapists in terms of adherence to the protocol, measured by the score of an independent rater on an a-priori established adherence rating protocol; a higher score reflects better adherence. Minimum=0 ;maximum=100

Participants acceptability

时间窗: 1 year

The acceptability of AF-EMDR to participants in terms of compliance, measured by the total number of sessions attended and the proportion of attended versus non attended (planned) sessions; a higher proportion of attended sessions reflects better compliance.

Study adherence of participants

时间窗: 1 year

from randomization until follow-up in terms of completion of tasks. A higher amount of completion means a better outcome.

Experienced (by participants) acceptability and burden

时间窗: 1 year

The number of experienced facilitators and barriers and subjective effectiveness of the AF-EMDR intervention.

次要结局

  • Change in Level of Urge (LoU)(1 year)
  • Change in: Level of Positive Affect (LoPA)(1 year)
  • Change in: Subjective Units of Distress (SUD)(1 year)
  • changes in: Positive incentive value (SCCQ)(1 year)
  • changes in: Substance use (past 30 days) (MATE section 1)(1 year)
  • changes in: Craving-related self-control/self-efficacy (SCCQ)(1 year)
  • Change in craving(1 year)
  • changes in: Craving (MATE Q1: OCDS-5)(1 year)

研究者

发起方
IrisZorg
申办方类型
Other
责任方
Sponsor

研究点 (2)

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