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临床试验/ACTRN12622000131752
ACTRN12622000131752已完成未知

A randomised controlled trial evaluating the effectiveness of a CBT-based smartphone application for improving depressive symptoms and other mental health outcomes in young people

niversity of New South Wales (UNSW)0 个研究点目标入组 569 人开始时间: 2022年1月27日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
569

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 17 Years(—)
性别
All

入选标准

  • Aged 12 to 17 years (confirmed by self-report);
  • Located in Australia (confirmed by self-report);
  • Experiencing mild to moderately-severe depressive symptoms (as determined by a total score of 5-19 on the self-report Patient Health Questionnaire-9- Adolescent version);
  • Own or have access to a smartphone (for receipt of the study interventions);
  • Have access to the Internet, an active email address and mobile phone number (for receipt of study activities, invitations, reminders);
  • Comfortable with reading English at Year 7-8 level (to ensure comprehension of intervention content);
  • Have a parent or guardian who can provide consent for participation.

排除标准

  • Currently experiencing severe suicidal ideation (as determined by a score of greater than or equal to 2 on item 9 of the self-report Patient Health Questionnaire-9-Adolescent version).
  • Had serious suicidal ideation in the past month (as determined by self-report).
  • A suicide attempt in the past month (as determined by self-report).
  • Experiencing nil or severe depressive symptoms (as determined by a score total of less than or equal to 4 or greater than or equal to 20 on the self-report Patient Health Questionnaire).
  • Currently receiving OR about to start (in the next 2 weeks) any psychological treatment for feelings of low mood or depression from a psychologist, psychiatrist or other mental health professional
  • Currently taking OR about to start (in the next 2 weeks) any daily prescribed medication (e.g., anti-depressants) for their mental health (low mood, depression or anxiety).
  • Unable to gain parental consent to participate (as determined by failure to return parental consent form within their recruitment period).
  • Located outside of Australia, not within age range or fail to satisfy any of the other inclusion criteria (as determined by the self-report screener).

研究者

发起方
niversity of New South Wales (UNSW)

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