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Can an AI chatbot cure social anxiety? new study tests smartphone therapy

NCT ID NCT07533812

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This pilot study tests two 4-week smartphone treatments for social anxiety, one using psychodynamic therapy and the other cognitive behavioral therapy, both guided by an AI chatbot instead of a human therapist. 90 adults with social anxiety are randomly assigned to one of the two treatments or a waitlist. Participants complete weekly questionnaires to track changes in anxiety and mood.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
AI chatbot delivering psychotherapy modules
What this could lead to
If successful, this could point toward a scalable, low-cost digital treatment for social anxiety that doesn't require a human therapist.
What could go wrong
This is a small pilot study with only 90 participants and no long-term follow-up. The AI chatbot may not be as effective as in-person therapy, and results may not apply to everyone.

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

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

About 90 people

The number the study aims to enrol. It can still change while the study runs.

Started

Apr 2025

Expected to finish

Jul 2026

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

* Age 18 years or older * Score of 30 or higher on the Liebowitz Social Anxiety Scale-Self Report (LSAS-SR) * Access to a smartphone * Ability to read and write Swedish * Currently engaged in psychological treatment * Severe depression (Patient Health Questionnaire-9 score 20 or higher) * Use of medication for anxiety or depression if there have been changes within the past 30 days * Suicidality as assessed by the Columbia Suicide Severity Rating Scale (C-SSRS)

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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.

Contacts and locations

Locations

  • Stockholm university

    Stockholm, Stockholm County, 10691, Sweden

More trials for these conditions

Other studies related to the condition(s) this trial covers.