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Can a website replace the Therapist's couch? singapore tests online CBT for anxiety and depression

NCT ID NCT07532551

Symptom relief Sponsor: National University of Singapore Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Aug 06, 2026 · Updated 2 times

Summary

This study will test if an internet-based cognitive behavioral therapy (iCBT) program can help reduce symptoms of mild-to-moderate anxiety and depression in adults in Singapore. About 390 participants will either receive the 8-week online program with counselor check-ins or continue with their usual care. Researchers will measure symptom changes and compare costs to see if iCBT is a practical and affordable option for mental health support.

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 390 people

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

Started

Jul 2026

Expected to finish

Mar 2028

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

21 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.

1. Quantitative Study - Patients Inclusion Criteria: * Age ≥21 years * Tier 2 - 3 depression and/or anxiety based on PHQ-9 and GAD-7 scores * PHQ-9 score of 5 to 19 * GAD-7 score of 5 to 14 * Able to provide informed consent Exclusion Criteria: * Unable to read or understand English (Primary 6 level) * Unable to use the internet (e.g. due to lack of internet access or insufficient digital literacy) * Does not possess a mobile device or is not able to access the iCBT application * Actively experiencing psychosis * Suspected with personality disorder * Primary concern is obsessive compulsive disorder (OCD) * Tier 4 patients with severe depression or anxiety * PHQ-9 score of 20 and above * GAD-7 score of 15 and above * Any suicidal risk or ideation * PHQ-9 Question 9 score of more than 2 2. Qualitative Study - Service Providers Inclusion Criteria: * Are currently or previously have been involved in the delivery, supervision, or implementation of the iCBT programme * Have had direct experience supporting patients enrolled in the study * Able to provide informed consent Exclusion Criteria: * Have no direct involvement in the iCBT programme; or * Have had insufficient exposure to the programme, defined as managing fewer than one referred case or less than one month of involvement at the time of recruitment. * Conflict of interest or Supervisory Hierarchy Concerns - Individuals whose participation may create perceived coercion or introduce bias * Inability to provide informed consent

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Conditions

The condition(s) this trial relates to.

anxiety anxiety disorder Depression depressive disorder mixed anxiety and depressive disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Cognitive behavioral therapy Depression and/or anxiety in the mild-to-moderate range

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    3 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • [Allkin] Integrated Service Centre @ Sengkang 193

    RECRUITING

    Singapore, 540193, Singapore

  • [Fei Yue] Family Service Centre (Choa Chu Kang)

    RECRUITING

    Singapore, 680280, Singapore

  • [Viriya] Mental Wellness Hub

    RECRUITING

    Singapore, 210052, Singapore

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