跳至主要内容
临床试验/NCT04277793
NCT04277793已完成不适用

Feasibility Evaluation of a Monitored Self-guided Digital Cognitive Behavioural Therapy Format: an Uncontrolled Trial of a Problem Solving Intervention for Depression and Anxiety

Karolinska Institutet1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2020年4月24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
12
试验地点
1
主要终点
Treatment Credibility Scale

研究概览

简要总结

The purpose of the study is to evaluate the feasibility of a new monitored self-guided digital cognitive behavioural therapy format through one of the key components of an intervention for depression and anxiety (Problem Solving) and to answer the question: Do patients with significant levels of depression and/or anxiety symptoms consider the monitored self-guided digital format usable and credible? An uncontrolled trial will explore participant's usability and treatment credibility ratings.

详细描述

Objective. The purpose of the study is to evaluate the feasibility of a new monitored self-guided digital cognitive behavioural therapy format through one of the key components of an intervention for depression and anxiety (Problem Solving) and to answer the question: Do patients with significant levels of depression and/or anxiety symptoms consider the monitored self-guided digital format usable and credible?

Background. Problem Solving is a behavioral modification intervention focusing on the training of adaptive problem-solving skills in order to cope more effectively with everyday stressful events. It is one of the most well-examined therapeutic interventions for depression, with reliable support regarding symptom improvement in depression traditionally delivered with therapist-guidance when administered via the Internet. Since a new monitored self-guided digital intervention for depression and anxiety has been developed, including the key component Problem Solving, it is of importance to assess both the usability and treatment-credibility of this format to evaluate if it is feasible.

Methodology. Based on similar feasibility studies including around ten participants, a number of 16-30 participants will be included in this study to compensate for potential drop-outs. Participants will be recruited via a psychiatric clinic belonging to Stockholm County Council in Stockholm, Sweden, and will be patients in queue for treatment for depression and/or anxiety in a psychiatric setting. Inclusion criteria will be significant depression and/or anxiety symptoms. The participants included in the study will access the key component Problem Solving during four weeks while being on waitlist for regular treatment. They will be introduced to the intervention as a self-explanatory tool with possible beneficial effects on depression symptoms. Self-assessments will be carried out during the intervention. The scores on these scales will be compared to available published data from these scales from evaluations of therapist-guided Internet-based interventions if available, and otherwise data from these scales from studies on other digital interventions for mental health. The participants will also answer questions concerning their experience of the format.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • Significant depression and/or anxiety symptoms measured with Patient Health Questionnaire (PHQ-9) and General Anxiety Disorder (GAD-7) (i.e. a PHQ-9 and/or GAD-7 score of ≥5).

排除标准

  • insufficient Swedish knowledge
  • minor (i.e. age <18 years)
  • high suicide risk (i.e. a score ≥4 on the ninth item on the Montgomery Åsberg Depression Scale, MADRS-S)
  • lack of access to a device with Internet connection (e.g. computer, mobile, tablet)
  • lack of access to a phone on which calls and SMS can be received
  • psychiatric or somatic problems that must be prioritized before or become an excessive obstacle to the intervention.

结局指标

主要结局

Treatment Credibility Scale

时间窗: immediately after the intervention

Self-rated assessment of treatment credibility, higher score is better

System Usability Scale

时间窗: immediately after the intervention

Self-rated assessment of usability, higher score is better

次要结局

  • System Usability Scale(During the intervention: 2 weeks from baseline)
  • Negative Effects Questionnaire(During the intervention: 2 weeks from baseline)
  • Patient Health Questionnaire - 9(Change from baseline immediately after the intervention)
  • Generalized Anxiety Disorder - 7(Change from baseline immediately after the intervention)
  • Treatment Credibility Scale(During the intervention: 2 weeks from baseline)

研究者

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

Martin Kraepelien

Licensed clinical psychologist, Principal investigator, PhD

Karolinska Institutet

研究点 (1)

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