跳至主要内容
临床试验/NCT04260750
NCT04260750已完成不适用

ICBT for Depression - A Factorial Investigation of Kinds of Therapist Support and Self-/Expert-selected Content

Linkoeping University2 个研究点 分布在 1 个国家目标入组 246 人开始时间: 2020年1月13日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
246
试验地点
2
主要终点
Change on Patient Health Questionnaire (PHQ-9)

研究概览

简要总结

The study is a factorial randomized controlled trial investigating the efficacy of difference versions of internet-administered cognitive behavioral therapy.

详细描述

The study is a 2 x 2 design. The first factor thought to be of relevance for the efficacy is the whether the content is selected by the participants themselves or by a therapist. The second factor consists of two levels: regular, continuous weekly support from a therapist or guidance on demand by a health care team consisting of a physician, a nurse, a clinical psychologist, an IT-technician and the principal investigator of the study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
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

  • Current depressive symptoms equivalent to a score of at least 5 on Patient Health Questionnaire 9 and a minimum of 10 points on Becks Depression Inventory.
  • 18 years or older.
  • Adequate ability to understand and speak Swedish.
  • Access to the internet and a smartphone/computer.

排除标准

  • Other ongoing psychological treatment or counselling.
  • Recent (within the past 3 months) changes in the dose of psychotropic medication.
  • Prior diagnosis of psychosis, bipolar disorder, or substance dependence.

结局指标

主要结局

Change on Patient Health Questionnaire (PHQ-9)

时间窗: Baseline, during week 1, 2, 3, 4, 5, 6, 7, 8, 9, and 10 of the intervention, post-intervention (after 11 weeks), 12 months after the end of intervention.

Measure of depressive symptoms. Possible range for the total sum: 0 to 27 (created by summing up the score from each item). Clinical cut-offs for mild, moderate, moderately severe and severe major depressive disorder are considered to be 5, 10, 15, and 20 points.

Change on Becks Depression Inventory-II (BDI-II)

时间窗: Baseline, after the intervention (after 11 weeks), 12 months after the end of intervention.

Measure of depressive symptoms. Possible range for the total sum: 0 to 63 (created by summing up the score from each item). Clinical ranges for minimal, mild, moderate and severe major depressive disorder are considered to be 0-13, 13-19, 20-28, and 29-63 points.

次要结局

  • Change on Generalised Anxiety Disorder 7-item scale (GAD-7)(Baseline, after the intervention (after 11 weeks), 12 months after the end of intervention.)
  • Change on Brunnsviken Brief Quality of Life Scale (BBQ)(Baseline, after the intervention (after 11 weeks), 12 months after the end of intervention.)
  • Change on Insomnia Severity Index (ISI)(Baseline, after the intervention (after 11 weeks), 12 months after the end of intervention.)

研究者

发起方
Linkoeping University
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Gerhard Andersson

Professor

Linkoeping University

研究点 (2)

Loading locations...

相似试验