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临床试验/NCT05617248
NCT05617248已完成不适用

Feasibility and Efficacy of a Brief Digital Self-efficacy Training in University Students With Self-reported Elevated Stress: A Randomized Controlled Trial

University of Zurich1 个研究点 分布在 1 个国家目标入组 94 人开始时间: 2020年5月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
94
试验地点
1
主要终点
General self-efficacy

研究概览

简要总结

The study investigates the effects of a digital, scalable self-efficacy training of repeated recall of self-efficacy memories on mental health outcomes, such as self-efficacy, anxiety, stress, hopelessness, and other mental health outcomes. A total of 94 students with elevated stress levels (≤ 13 on the Perceived Stress Scale) will be recruited and randomly assigned to training and control group. Individuals will either engage in the self-efficacy training app combined with Ecological Momentary Assessment (EMA) for 1 week (training group) or in EMA only for 1 week (control group). Baseline and post assessments will measure changes in self-efficacy, anxiety, stress, hopelessness, and other mental health outcomes.

详细描述

Self-efficacy is associated with positive mental health outcomes and has been proposed as a putative contributor to therapeutic outcomes in the treatment of mental health problems. It can be enhanced through experimental inductions and the recall of autobiographical mastery experiences, which have mostly been conducted in person and in the laboratory until today.

The study will investigate effects of a digital, scalable self-efficacy training of repeated recall of self-efficacy memories on mental health outcomes, such as self-efficacy, anxiety, stress, hopelessness, and other mental health outcomes. The study will recruit 94 students with elevated stress levels (≤ 13 on the Perceived Stress Scale) and randomly assigned them to training and control group. Individuals will either engage in the self-efficacy training app combined with Ecological Momentary Assessment (EMA) for 1 week (training group) or in EMA only for 1 week (control group). Baseline and post assessments will measure changes in self-efficacy, anxiety, stress, hopelessness, and other mental health outcomes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Outcomes Assessor)

盲法说明

Assessors are blind to individuals' reports of perceived stress prior to and following the intervention, i.e. at all assessment times.

入排标准

年龄范围
18 Years 至 29 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •being enrolled at a Swiss university
  • •aged between 18 and 29 years
  • •experiencing at least moderate stress (score of ≥13 on the Perceived Stress Scale
  • •owning a smartphone
  • •speaking fluent German

排除标准

  • •current psychiatric disorder

研究组 & 干预措施

Experimental: Self-efficacy training (App)

Experimental

This group will receive a digital one week self-efficacy training with three training sessions per day and EMA (10 per day).

干预措施: Self-efficacy App (Behavioral)

Control

No Intervention

This group will receive EMA questionnaires for one week (10 per day).

结局指标

主要结局

General self-efficacy

时间窗: change from baseline to 1 day post intervention; time frame: 1 week

The General Self-Efficacy Scale (Schwarzer \& Jerusalem, 1995; Tipton \& Worthington, 1984) will measure the general self-efficacy.

次要结局

  • Positive and negative affect(The Positive and Negative Affect Scale (Krohne, Egloff, Kohlmann, & Tausch, 1996; Watson, Clark, & Tellegen, 1988) will measure positive and negative affect.)
  • Perceived stress(change from screening to 1 day post intervention; time frame: 1 week)
  • Hope(change from baseline to 1 day post intervention; time frame: 1 week)
  • Depression(The Beck Depression Inventory-II (Beck, Steer, Ball, & Ranieri, 1996; Kuhner, Burger, Keller, & Hautzinger, 2007) will measure depression.)
  • Anxiety(change from baseline to 1 day post intervention; time frame: 1 week)
  • Hopelessness(change from baseline to 1 day post intervention; time frame: 1 week)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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