跳至主要内容
临床试验/NCT04982796
NCT04982796进行中(未招募)1 期

Psilocybin-Enhanced Psychotherapy for Methamphetamine Use Disorder

Portland VA Research Foundation, Inc2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年7月7日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
30
试验地点
2
主要终点
Acceptability

研究概览

简要总结

This is a proof-of-concept randomized clinical trial of psilocybin-enhanced psychotherapy versus treatment-as-usual among individuals being treated for methamphetamine use disorder.

详细描述

The trial will take place with individuals admitted to a residential rehabilitation treatment program. The treatment protocol will consist of 4 preparatory therapy visits, 2 psilocybin sessions (25-30mg), and 8 total integration therapy visits. Primary aims assess acceptability, feasibility, and safety with a primary endpoint at the conclusion of the study intervention. An additional aim assesses preliminary efficacy for methamphetamine use disorder and overall functioning at follow-up assessments 60 and 180 days after discharge from the residential treatment program.

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)

盲法说明

Clinical interviewers will be blinded to condition and study timepoint.

入排标准

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

入选标准

  • United States military Veteran
  • Moderate to severe methamphetamine use disorder using the DSM-V diagnostic criteria
  • Desire to cease or reduce methamphetamine use

排除标准

  • Have uncontrolled hypertension or clinically significant cardiovascular disease
  • History of seizure disorder in adulthood
  • CNS metastases or symptomatic central nervous system (CNS) infection
  • Poorly controlled diabetes mellitus
  • Taking certain medications that may interact with psilocybin
  • History of any primary persistent psychotic disorder, including schizophrenia, schizoaffective disorder, bipolar disorder with psychosis, major depressive disorder with psychosis, or schizophreniform disorder
  • History of bipolar I disorder
  • Current eating disorder with active purging
  • History of hallucinogen use disorder
  • Pregnant or breast feeding

研究组 & 干预措施

Treatment-as-Usual

Other

Treatment-as-usual while admitted to a residential rehabilitation treatment program.

干预措施: Treatment-as-usual (Behavioral)

Psilocybin-enhanced psychotherapy

Experimental

Psilocybin will be administered twice (25mg & 30mg two weeks apart) in addition to a 6-week psychotherapy protocol while admitted to a residential rehabilitation treatment program.

干预措施: Treatment-as-usual (Behavioral)

Psilocybin-enhanced psychotherapy

Experimental

Psilocybin will be administered twice (25mg & 30mg two weeks apart) in addition to a 6-week psychotherapy protocol while admitted to a residential rehabilitation treatment program.

干预措施: Psilocybin (Drug)

结局指标

主要结局

Acceptability

时间窗: End of 6-week intervention; approximately 42 days

We will use a 7-point Likert scale to measure each participant's perceived benefit and perceived harm of the intervention.

Proportion of patients who complete the intervention and follow-up

时间窗: End of 6-week intervention to 180 days post-discharge follow-up; approximately 180 days

We will observe the proportion of patients who complete the intervention and follow-up to determine feasibility.

次要结局

  • Change from baseline in Sheehan Disability Scale at 60 day post-discharge follow-up(approximately 102 days post-enrollment)
  • Change from baseline in Sheehan Disability Scale at 180 day post-discharge follow-up(approximately 222 days post-enrollment)
  • Methamphetamine Use, urine(180 days post-discharge follow-up; approximately 222 days post-enrollment)
  • Change from baseline in Sheehan Disability Scale (SDS) at end-of-intervention(approximately 42 days post-enrollment)
  • Methamphetamine Use, self-report(180 days post-discharge follow-up; approximately 222 days post-enrollment)
  • Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability](180 day post-discharge follow-up; approximately 222 days post-enrollment)
  • Methamphetamine Use, self-report(60 days post-discharge follow-up; approximately 102 days post-enrollment)
  • Methamphetamine Use, urine(60 days post-discharge follow-up; approximately 102 days post-enrollment)

研究者

发起方
Portland VA Research Foundation, Inc
申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验