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临床试验/NCT03272516
NCT03272516已完成不适用

Mindfulness Based Cognitive Therapy (MBCT) for Primary Care Patients With Mild to Moderate Symptoms of Depression or Anxiety.

University of Iceland4 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2017年9月12日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
120
试验地点
4
主要终点
Symptoms of depression measured with the PHQ-9 questionnaire

研究概览

简要总结

This study is done to evaluate the effects of Mindfulness Based Cognitive Therapy (MBCT) for primary care patients that have mild to moderate symptoms of depression and anxiety. Half of the study participants will receive treatment as usual (TAU), and the other half will receive TAU plus MBCT. The investigators will be comparing changes in symptoms of depression and anxiety between the groups, and hypothesize that the TAU plus MBCT group will have significantly lower symptoms of depression and anxiety compared to TAU group post-intervention

详细描述

Patients that show mild to moderate symptoms of depression and anxiety are common in the primary care setting. These patients are often treated with antidepressant or anxiolytic medication instead of cognitive therapy, which is the first choice of treatment according to clinical guidelines in Iceland. Although these patients are often referred to cognitive therapy, there are long waiting lists for group therapy and personal therapy is expensive. MBCT has been shown to have good effects on people with recurrent depression and on patients suffering from anxiety. Therefore, the investigators main objective is to assess whether MBCT is effective in the primary care setting for patients with mild symptoms of anxiety and depression and compare its effect to TAU.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Investigator)

盲法说明

The investigator will contact all participants in both groups via email or telephone to ask them to answer questionnaires.The investigator will not have information about which group which participant is. Participants will be contacted and invited to answer a questionnaire before, after, 6 and 18 months after 8 weeks of TAU and TAU plus MBCT.

入排标准

年龄范围
18 Years 至 67 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • PHQ-9 and GAD-7 score 5-14 points
  • Age18 - 67
  • No current/recent psychotherapy of any kind other than his/hers physicians therapy( can be taking antidepressants but not in CBT)
  • No regular meditation or yoga practice
  • Not mentally retarded
  • Speaks and understands Icelandic
  • No current substance dependence
  • Not diagnosed with schizophrenic symptoms or bipolar disease that that currently requires treatment
  • Not participating in another mental health study

排除标准

  • Age: <18 and >67 years old.
  • Severe psychiatric symptoms requiring psychiatric care
  • Risk of suicide
  • Inability to participate in group sessions because of severe substance misuse;
  • Inability to speak and understand Icelandic
  • Current psychotherapy of any kind;
  • Participation in any other psychiatric intervention study;
  • Thyroid disease (if newly diagnosed by the doctor).
  • Score under 5 on both GAD7 and PHQ-9 and score over 14 on either GAD7 or PHQ-
  • One or more of the following ICD-10 psychiatric diagnoses:
  • F00-F09 Organic, including symptomatic, mental disorders F10-F19 Mental and behavioural disorders due to psychoactive substance use F20-F29 Schizophrenia, schizotypal and delusional disorders F70-F79 Mental retardation

结局指标

主要结局

Symptoms of depression measured with the PHQ-9 questionnaire

时间窗: up to 18 months

Comparing scores on the PHQ-9 before and after the intervention as well as, 6 and 18 months after the intervention for both the control group (TAU) and the intervention group (TAU plus MBCT)

Symptoms of anxiety measured with the GAD-7 questionnaire

时间窗: up to 18 months

Comparing scores on the GAD-7 before and after the intervention as well as 6 and 18 months after the intervention for both the control group (TAU) and the intervention group (TAU plus MBCT)

次要结局

  • Subjective well-being measured with the SWEMWBS questionnaire(up to 18 months)
  • Change in use of antidepressants(up to 18 months)
  • Change in use of anxiolytics(up to 18 months)

研究者

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

Svala Sigurdardottir

Principal Investigator

University of Iceland

研究点 (4)

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