Can an online course ease anxiety and depression? new study aims to find out
NCT ID NCT07177365
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tests whether an 8-week internet-based cognitive behavioral therapy (ICBT) program can help adults with generalized anxiety disorder or major depressive disorder. Participants in Taiwan will either receive standard care alone or standard care plus the online program, which includes 12 modules on skills like cognitive restructuring and mindfulness. The goal is to see if ICBT improves symptoms and makes therapy more accessible.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Internet-based cognitive behavioral therapy (ICBT)
- What this could lead to
- If it works, this could provide a convenient, low-cost online treatment option for anxiety and depression, reducing the need for frequent clinic visits.
- What could go wrong
- This is a relatively small trial (120 participants) and results may not apply to everyone. The therapy is self-guided online, so some people may not engage fully or benefit as much as with in-person sessions.
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 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2025
An estimate. Start dates often move.
- Expected to finish
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Jun 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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20 to 65 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: * Age between 20 and 65 years. * Diagnosis of Generalized Anxiety Disorder (GAD) confirmed by a psychiatrist. * Diagnosis of Major Depressive Disorder (MDD) confirmed by a psychiatrist, without acute suicidal risk (screened by PHQ-9 Item 9; score of 3 requires further clinical assessment to exclude active suicidal plan or recent self-harm). Exclusion Criteria: * For GAD ICBT participants * Current or past history of obsessive-compulsive disorder, panic disorder, bipolar disorder, eating disorder, schizophrenia, or substance abuse. * Severe depressive symptoms impairing daily functioning. * Current suicidal ideation. * Experiencing acute life stressors (e.g., domestic violence, ongoing treatment for serious physical illness). * Currently receiving psychological counseling or psychotherapy. * Other serious factors limiting participation (e.g., intellectual disability, significant cognitive impairment, severe vision or hearing impairment). * For MDD ICBT participants * Diagnosis of bipolar disorder, eating disorder, schizophrenia, psychotic symptoms, or substance abuse. * Current suicidal ideation or recent self-harm (PHQ-9 Item 9 score of 3 triggers further assessment; exclusion if active suicidal plan or recent self-harm present). * Experiencing acute life stressors (e.g., domestic violence, ongoing treatment for serious physical illness). * Currently receiving psychological counseling or psychotherapy. * Other serious factors limiting participation (e.g., intellectual disability, significant cognitive impairment, severe vision or hearing impairment).
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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 official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
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