Skip to content

Feasibility and Efficacy of a Brief Digital Self-efficacy Training

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05617248
Acronym
SEAPP
Enrollment
94
Registered
2022-11-15
Start date
2020-05-18
Completion date
2020-11-09
Last updated
2022-11-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Self Efficacy, Stress

Keywords

self-efficacy, stress, digital, intervention

Brief summary

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.

Detailed description

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.

Interventions

BEHAVIORALSelf-efficacy App

The training starts with a psychoeducational video and instructions to define two autobiographical self-efficacy The individuals will then receive three self-efficacy trainings per day based on their autobiographical memories and combined with a slow breathing exercise. Additionally, they will receive 10 daily EMA questionnaires on mood, social contacts, and virtual context.

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

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

Intervention model description

Randomised controlled trial testing a brief digital intervention (SeApp) against a control group receiving only EMA

Eligibility

Sex/Gender
ALL
Age
18 Years to 29 Years
Healthy volunteers
Yes

Inclusion criteria

* 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

Exclusion criteria

-current psychiatric disorder

Design outcomes

Primary

MeasureTime frameDescription
General self-efficacychange from baseline to 1 day post intervention; time frame: 1 weekThe General Self-Efficacy Scale (Schwarzer & Jerusalem, 1995; Tipton & Worthington, 1984) will measure the general self-efficacy.

Secondary

MeasureTime frameDescription
Positive and negative affectThe Positive and Negative Affect Scale (Krohne, Egloff, Kohlmann, & Tausch, 1996; Watson, Clark, & Tellegen, 1988) will measure positive and negative affect.change from baseline to 1 day post intervention; time frame: 1 week
Hopechange from baseline to 1 day post intervention; time frame: 1 weekThe Trait Hope Scale (Krause, 2002; Snyder et al., 1991) will measure hope.
DepressionThe Beck Depression Inventory-II (Beck, Steer, Ball, & Ranieri, 1996; Kuhner, Burger, Keller, & Hautzinger, 2007) will measure depression.change from baseline to 1 day post intervention; time frame: 1 week
Anxietychange from baseline to 1 day post intervention; time frame: 1 weekState-Trait Anxiety Inventory (Laux, Glanzmann, Schaffner, & Spielberger, 1981; Spielberger, Gorsuch, Lushene, Gagg, & Jacobs, 1983) will measure state and trait anxiety.
Hopelessnesschange from baseline to 1 day post intervention; time frame: 1 weekThe Beck Hopelessness Scale (Beck, Weissman, Lester, & Trexler, 1974; Kliem, Lohmann, Mossle, & Brahler, 2018) will measure hopelessness.
Perceived stresschange from screening to 1 day post intervention; time frame: 1 weekThe Perceived Stress Scale (Cohen, Kamarck, & Mermelstein, 1983; Klein et al., 2016) will measure perceived stress.

Other

MeasureTime frameDescription
Specific self-efficacydaily measured in training group only; changes in the course of the study participationSpecific self-efficacy will be captured once per day. Questions will focus on e. g. the participant's level of agreement with statements such as Right now, I think I will be able to do what is necessary to make this training successful.
Virtual contextdaily measured; changes in the course of the study participationEMA will capture virtual context at 10 time points per day during the one week study participation. Questions will be about who the person is with and how they feel about it.
Dissatisfaction with social contactsdaily measured; changes in the course of the study participationEMA will capture dissatisfaction with social contacts at 10 time points per day during the one week study participation. There will be two options indicating dissatisfaction with social contacts: (a) being with nobody and feeling excluded or wanting to be with someone or (b) being with someone and rather wanting to be alone. We combined these into one variable.
Positive and negative affectDaily measured; changes in the course of the study participationEMA will capture positive and negative mood at 10 time points per day during the one week study participation. We will measure positive mood using three items (cheerful, happy, and relaxed) and negative mood using seven items (irritated, anxious, insecure, lonely, sad, overthinking, and stressed).

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026