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临床试验/NCT05560581
NCT05560581招募中不适用

Digital Self-efficacy Training to Bridge Waiting Times for Psychotherapy

Psychiatric University Hospital, Zurich2 个研究点 分布在 1 个国家目标入组 94 人开始时间: 2022年11月7日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
94
试验地点
2
主要终点
Change in self-efficacy

研究概览

简要总结

The main aim of this project is to improve waiting periods for specialised psychotherapy. We will apply a brief, smartphone-based self-efficacy training to patients with psychiatric disorders waiting for specialised psychotherapy. Additionally, we will use Ecological Momentary Assessment (EMA) to assess mood, social contacts, and other parameters daily. We will investigate whether the training can improve self-efficacy and related constructs and if it can help reduce stress and waitlist drop-outs during waiting periods. Additionally, we will investigate if the self-efficacy training has a positive effect on motivation and therapeutical relationship regarding the subsequent therapy.

After a screening for eligibility, participants will be randomly assigned to intervention and control group. At baseline, participants attend a laboratory session where they are assessed for current psychiatric disorders and further relevant psychological variables. They will then either participate in the digital self-efficacy training combined with EMA (intervention group) or in EMA only (control group). Both will be conducted via a smartphone app. Subsequently, participants will be asked to fill in post questionnaires at three different time points: after having finished app usage, one month later, and after the beginning of the subsequent psychotherapy.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

double-blind

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •psychiatric disorder
  • •age 18-65
  • •waiting for psychiatric assessment/treatment (being on waitlist)
  • •sufficient knowledge of the German language
  • •smartphone user
  • •internet access via smartphone
  • •internet access at home (laptop, tablet, or computer)

排除标准

  • •current intense psychotherapy
  • •acute suicidality
  • •acute psychotic symptoms
  • •substance addiction

研究组 & 干预措施

Intervention group

Experimental

Participants will receive an one-week digital self-efficacy training (3x/day) and an one-week Ecological Momentary Assessment (3x/day questions on mood, social and virtual contacts).

干预措施: Digital self-efficacy training (Behavioral)

Intervention group

Experimental

Participants will receive an one-week digital self-efficacy training (3x/day) and an one-week Ecological Momentary Assessment (3x/day questions on mood, social and virtual contacts).

干预措施: Ecological Momentary Assessment (Behavioral)

Control group

Active Comparator

Participants will receive an one-week Ecological Momentary Assessment (3x/day questions on mood, social and virtual contacts).

干预措施: Ecological Momentary Assessment (Behavioral)

结局指标

主要结局

Change in self-efficacy

时间窗: baseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy began

Validated measures ("General Self-Efficacy Scale" (10 items; higher scores indicate higher self-efficacy -\> better outcome), "Coping Self-efficacy scale" (26 items; higher scores indicate higher self-effiacy -\> better outcome) and individual questions based on validated measures assessing specific self-efficacy regarding emotion regulation, therapy and waitlist will be used to assess self-efficacy at baseline and 3 different time points after the intervention.

次要结局

  • Change in hopelessness(baseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy began)
  • Change in stress(baseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy began)
  • Change in anxiety(baseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy began)
  • Change in therapy expectations(baseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy began)
  • Change in intolerance of uncertainty(baseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy began)
  • Change in depression(baseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy began)
  • Change in optimism(baseline to 1 day after the intervention, 1 month after the intervention, within 1 month after the subsequent therapy began)

研究者

发起方
Psychiatric University Hospital, Zurich
申办方类型
Other
责任方
Principal Investigator
主要研究者

Judith Rohde, MD

Clinician Scientist

Psychiatric University Hospital, Zurich

研究点 (2)

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