Digital strategies to improve help-seeking for youth at risk of psychosis
Official title: Digital Strategies to Advance Help-Seeking in Youth at Clinical High Risk for Developing Psychosis
Run by Columbia University · NCT06774430 · Data updated 2026-11-12
This study is testing new digital tools to help young people aged 12-29 who are at risk for psychosis find the support they need and start treatment faster.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 12 Years to 29 Years |
| Sex | All |
| Enrollment | 25000 (estimated) |
| Sponsor | Columbia University Academic / other |
| Locations | 1 site (New York, New York) |
| Status | Recruiting |
| Started | April 7, 2025 |
| Main results expected | May 31, 2028 |
| Study ends | May 31, 2028 |
| Registry record updated | May 5, 2026 |
| Trial ID | NCT06774430 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are youth aged 12-29 who live within a 50-mile radius of a participating AMP-SCZ site and can complete the English language PQ-B screening.
✕Probably not a fit
Patients outside the age range of 12-29 or those who do not live near an AMP-SCZ site may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to create a Digital Laboratory to enhance help-seeking behaviors and speed up treatment initiation for youth aged 12-29 who are at Clinical High Risk for developing psychosis. By utilizing the Health Action Process Approach (HAPA) model, the study will analyze help-seeking patterns in 25,000 youth who screen positive for psychosis risk. It will employ Micro-Randomized Trials and a Sequential Multiple Assignment Randomized Trial to develop personalized strategies for advancing help-seeking and will link participants to local clinical care through a national network. The study seeks to establish effective thresholds for identifying clinical high risk online and to curate a large dataset of youth with CHR.
Why it matters
Potential benefit: If successful, this study could significantly improve early intervention and treatment outcomes for youth at risk of developing psychosis.
How similar studies have gone: Other studies have shown promise in using digital strategies for mental health interventions, but this approach is novel in its specific focus on youth at risk for psychosis.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Ages 12-29 years * Living within a 50-mile radius of a US based AMP-SCZ site * Able to complete the English language PQ-B on MHA's screening platform
Where it's running
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Columbia University Irving Medical Center
New York, New York, United States Recruiting
Study contacts
- Principal investigator: Michael Birnbaum, MD — Columbia University
- Study coordinator: Michael Birnbaum, MD
- Email: mlb2216@cumc.columbia.edu
- Phone: 212-523-2154
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Digital tools to help youth seek care sooner when at risk for psychosis
This project will test personalized digital messages and online strategies to help people ages 12–29 who screen positive for psychosis risk find and start local care sooner.
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State Representation in Early Psychosis 2
This observational study tests how people with early psychosis and healthy individuals use state information during tasks and how brain activity supports it.
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BRAVE program to reduce violence risk in early psychosis
A CBT-based program called BRAVE is tested with young adults in early psychosis to see if it is feasible and acceptable when added to usual care.
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On Track for Wellness: a stepped-wedge program to boost sleep and activity in first-episode psychosis
This program tests whether using Fitbit trackers, health education, and goal setting helps people with first-episode psychosis sleep better and move more.
-
Adding ketones to antipsychotics in young adults with first episode psychosis
This study tests whether giving exogenous ketones on top of antipsychotic treatment helps young adults experiencing a first episode of psychosis.
-
Add CBD to antipsychotic treatment for first-episode psychosis to see if it helps more than placebo
This study tests whether adding cannabidiol (CBD) to ongoing antipsychotic treatment helps people with a first episode of psychosis who haven’t fully responded to their first antipsychotic, compared with a placebo.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.