AI chatbot as a mental health ally for teens?
NCT ID NCT07778758
First seen Aug 21, 2026 · Last updated Aug 27, 2026 · Updated 2 times
Summary
This trial tests whether a virtual peer agent, VIPeerAgent, can help adolescents and young adults (ages 14-25) who are experiencing psychological distress but do not have a diagnosed mental disorder. Participants will be randomly assigned to chat with the AI agent, receive support from a human peer mentor, or get usual care. The study aims to see if the AI is as good as human support and better than no extra support, measuring outcomes like mental health status, resilience, and coping skills.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- VIPeerAgent, a virtual peer support agent that engages in multi-turn conversations to provide psychological support
- What this could lead to
- If effective, this could offer a scalable, accessible early intervention for youth mental health, potentially easing distress and building resilience.
- What could go wrong
- The trial is relatively small and early, and the AI may not match the nuance of human support. Risks include limited generalizability and potential for adverse effects from digital interactions.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 234 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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14 to 25 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adolescents and young adults aged 14-25 years. * Experienced at least one moderate or more severe stressful life event within the past 6 months. * Able to read and communicate in Chinese. * Willing to participate in the study and provide informed consent. * Have a BSI-53 score \<63. Exclusion Criteria: * A history of clinically diagnosed severe mental or psychiatric disorders, such as major depressive disorder or schizophrenia. * Current suicidal ideation or suicidal ideation within the past 6 months. * Receipt of professional psychological or psychiatric treatment within the past 12 months.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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School of Nursing, Sun Yat-Sen University
Guangzhou, Guangdong, 510080, China
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