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Clinical Trials in Germany / NCT07658547
Enrolling by invitation Observational

Use of AI Chatbots for Mental Health

NCT07658547 · tracked via the Priya Life Science Germany tracker
Phase
Observational
Started
2026-06
Last updated
2026-06-22

Condition(s) studied

Severe Mental Illness

Study summary

The goal of this observational study is to learn how patients with mental disorders use, perceive, and evaluate generative artificial intelligence (AI) chatbots for mental health-related purposes. The study aims to investigate usage patterns, expectations, experiences, perceived benefits, barriers, and concerns regarding AI chatbots among adults receiving psychiatric or psychotherapeutic treatment.

The main questions it aims to answer are:

* "How do patients with mental disorders use generative AI chatbots in the context of their mental health?"
* "What expectations, attitudes, and experiences do patients have regarding AI chatbots for mental health support?"

Participants will:

* Provide electronic informed consent before participation.
* Complete a one-time anonymous online survey lasting approximately 8 to 10 minutes.
* Answer questions about sociodemographic characteristics, psychiatric diagnoses, psychological distress, and digital device use.
* Report their expectations regarding AI chatbots for mental health support.
* Provide information about AI chatbot use, including frequency, duration, applications used, and purposes of use.
* Answer questions regarding satisfaction, trust, privacy concerns, perceived problems, and potential future integration of AI chatbots into mental health care.
* Optionally provide qualitative comments and suggestions in open-text fields.

There is no intervention, randomization, control group, or comparison arm in this study. The study follows a prospective cross-sectional mixed-methods design using quantitative survey data and qualitative free-text responses.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * diagnosed mental illness Exclusion Criteria: * incapable of giving consent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Immanuel Klinik Rüdersdorf Rüdersdorf Brandenburg

More Medizinische Hochschule Brandenburg Theodor Fontane trials in Germany

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07658547 on ClinicalTrials.gov ↗ ← All trials in Germany