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临床试验/ACTRN12619001522101
ACTRN12619001522101进行中(未招募)未知

INTEGRATE: An integrated treatment to decrease psychological distress and substance use in young people seeking help for emerging mental illness.

Orygen0 个研究点目标入组 71 人开始时间: 2019年11月4日最近更新:

试验速览

阶段
未知
状态
进行中(未招募)
发起方
入组人数
71

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
12 Years 至 25 Years(—)
性别
All

入选标准

  • Aged 12-25 years inclusive;
  • Seeking treatment at headspace for mental ill-health;
  • At screening, either:
  • Self-reported use during the past month of greater than or equal to 4x use of cannabis or alcohol, greater than or equal to 1x use of another illicit drug (e.g. methamphetamine, ecstasy, cocaine etc.), assessed using the Timeline Follow-back (TLFB; participants using alcohol only will be required to have consumed in excess of Australian National Guidelines for Alcohol Consumption of >4 standard drinks on greater than or equal to 1 occasion in the past month); OR
  • Self-reported, clinically-relevant binge alcohol use (i.e. at least 4 standard drinks on at least one occasion) in the past 3 months, which resulted in clear potential for harm or high-risk behaviour (i.e. blackouts, hospital attendance, driving while intoxicated);
  • Treatment with either a stable dose of an antidepressant or no antidepressant greater than or equal to 2 weeks at screening;
  • Sufficient English fluency to complete treatment and participate in the study;
  • Ability to provide written informed consent – where the participant is under 18 years of age, a parent or guardian will also be required to provide written informed consent or the young person will consent as a mature minor.

排除标准

  • Lifetime DSM-V diagnosis of a psychotic or bipolar disorder (assessed using structured clinical interview; SCID-5) OR current DSM-V diagnosis of either post-traumatic stress disorder, obsessive compulsive disorder, or an eating disorder for which the young person is seeking treatment;
  • Currently in AOD specific treatment, or open to referral to AOD treatment at headspace;
  • Current treatment with antipsychotic medication or mood stabiliser
  • Acute suicidality at screening, determined by clinical risk assessment;
  • Participation in another trial, which is likely to affect data for this study, determined by the Investigator;
  • Intellectual disability, as indicated by estimated or documented IQ of 70 or less.

研究者

发起方
Orygen

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