跳至主要内容
临床试验/NCT05250570
NCT05250570终止不适用

Distress Tolerance vs. Relaxation Therapy for Benzodiazepine Discontinuation in Patients Receiving Opioid Agonist Therapy

University of Pittsburgh3 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2022年6月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
1
试验地点
3
主要终点
Number of participants who discontinued BZDs at 4-month follow-up

研究概览

简要总结

The proposed study is a clinical trial, designed to pilot test a Distress Tolerance-Benzodiazepine Discontinuation (DT-BD) intervention for patients on opioid agonist therapy (OAT) who currently use benzodiazepines versus a Relaxation Therapy (RT) control condition. The DT-BD intervention is an adjunctive psychosocial intervention in people seeking to discontinue (BZD) use.

详细描述

This study pilot tests a 13-week distress tolerance-based psychosocial intervention paired with a benzodiazepine taper comparing it to a relaxation therapy control condition with the aim of assisting individuals receiving OAT discontinue benzodiazepine use. All participants will receive the same benzodiazepine (BZD) discontinuation protocol. The Distress Tolerance-Benzodiazepine Discontinuation (DT-BD) intervention consists of 13 weeks with 5 weekly therapy sessions prior to a 9-week BZD taper. Some participants may be prescribed non-benzodiazepine medications to treat the underlying conditions for which they were using BZDs [e.g. selective serotonin reuptake inhibitors (SSRI) for anxiety or hypnotics for insomnia]. Data collection will occur at baseline, then weekly for 13 weeks.

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
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
否

入选标准

  • •Age 18 or older
  • •Receiving OAT (methadone or buprenorphine) for at least 2 weeks
  • •Regular BZD use defined by BZD use 3 or more times per week in past month by self-report and positive urine screen at time of recruitment
  • •Provides permission to contact current BZD prescriber if being prescribed BZDs
  • •Speaks English
  • •Wants to discontinue BZD use
  • •Capacity to provide informed consent

排除标准

  • •Pregnant, confirmed by urine pregnancy test
  • •Cognitive impairment, as indicated by Montreal Cognitive Assessment (MoCA): must score at least 26 on the MoCA with a one-point adjustment for individuals with formal education of 12 years or fewer
  • •Any past month illicit opioid determined by self-report or urine drug test; illicit defined as non-medical use
  • •Receiving ongoing psychosocial treatment for BZD use disorder
  • •Uncontrolled seizure disorder (i.e. seizure in prior 90 days), or past BZD withdrawal seizure
  • •Current suicidality or homicidality
  • •Current psychotic symptoms

研究组 & 干预措施

Distress Tolerance - Benzodiazepine Discontinuation (DT-BD)

Experimental

This psychosocial treatment intervention uses a combination of interoceptive exposure therapy and elements of acceptance and commitment therapy (ACT) and psychoeducation about benzodiazepine use in OAT.

干预措施: Distress Tolerance - Benzodiazepine Discontinuation (DT-BD) (Behavioral)

Relaxation Therapy

Active Comparator

The relaxation therapy control condition involves psychoeducation about benzodiazepine use in OAT and progressive muscle-relaxation training.

干预措施: Relaxation Therapy (Behavioral)

结局指标

主要结局

Number of participants who discontinued BZDs at 4-month follow-up

时间窗: 4-months

Number of participants with BZD discontinuation defined by no BZD use by self-report during the month prior to 4-month follow-up corroborated by urine testing.

Number of participants who discontinued BZDs at 6-month follow-up

时间窗: 6-months

Number of participants with BZD discontinuation defined by no BZD use by self-report during the month prior to 6-month follow-up corroborated by urine testing.

次要结局

  • Change in quantity of BZD use(4- and 6-months)
  • Change in distress tolerance(4- and 6-months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Tae Woo Park

Assistant Professor

University of Pittsburgh

研究点 (3)

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