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Feasibility study of a chatbot-based training for stress reduction and health improvement

Feasibility study of a chatbot-based training for stress reduction and health improvement - Chatbot ELME

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00025446
Enrollment
30
Registered
2021-06-08
Start date
2021-06-14
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

The presence of a disease is not a prerequisite for participation in the study. People who want to try an innovative option in the context of a three-week psychological intervention to improve subjective stress experience and who currently have a moderate to high stress experience (PSS-10 score greater than or equal to 14).

Interventions

Group 1: Intervention group: conducts a three-week chatbot-based training consisting of two daily training sessions (á 10-20 min.) and questionnaires concerning the current well-being and stress exper
questionnaires concerning the current well-being and stress experience twice a day (á 5 min)

Sponsors

Abt. Klinische & Gesundheitspsychologie, Institut für Psychologie und Pädagogik, Universität Ulm
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Minimum age 18 years - Sufficient knowledge of written and spoken German - Consent to the study - Smartphone ownership (Android or iOS operating system) with internet access - Medium to high stress level (PSS-10 Score = 14) - Valid mobile phone number - Valid email address *Information concerning the sample size: the trial is running til that time point when the feasibility of the chatbot-based training is evaluable.

Exclusion criteria

Exclusion criteria: - Diagnosed mental illness - Current psychotherapy - Current online intervention to improve health-related parameters

Design outcomes

Primary

MeasureTime frame
Feasibility-related main outcome: Usability as assessed via the mHealth App Usability Questionnaire (MAUQ) at t2

Secondary

MeasureTime frame
Subjective stress Operationalisation: PSS-4 at measurement times t1, t2 and t3, between t1 and t2, Mindfulness (FFA) at measurement time points t1, t2, t3 Personality (BFI-10) at measurement time t1 Emotion regulation (ERQ) at measurement time t1, t2, t3 Well-being (WHO-5) at measurement time t1, t2, t3 Interoceptive Accuracy Scale (IAcc) at measurement times t1, t2, t3 Awareness scale of the Body Perception Questionnaire (BPQ) at measurement times t1, t2, t3 Attitude towards artificial intelligence (ATAI Scale) at measurement time points t1, t2, t3 Treatment Expectancy (CEQ) at measurement time t1 Stress Mindset Measure (SMM) at measurement time points t1, t2, t3 Generalised Anxiety Measure (GAD-7) at measurement time points t1, t2, t3 Satisfaction (ZUF-8) at measurement time t2 Negative effects (INEP) at measurement time points t2, t3 Affinity for technology (ATI) at measurement time t1 Open feedback questions on interaction with the chatbot at measurement time t2 Adherence (dropout during the study) at measurement time t1-t3

Countries

Austria, Germany, Switzerland

Contacts

Public ContactChristine Schillings

Abt. Klinische und Gesundheitspsychologie

elme-support@uni-ulm.de+49 (0)731 50 31738

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 11, 2026