How TikTok Trigger Warnings affect at-risk youth
Official title: Red Flag, Green Light: Exploring The Effect of TikTok Trigger Warnings in a Clinical Sample of Youth at Risk of Suicide
Run by Sunnybrook Health Sciences Centre · NCT07913854 · Data updated 2026-11-12
This study tests whether TikTok trigger warnings change how young people at risk of suicide feel and behave when they see suicide-related content.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 14 Years to 19 Years |
| Sex | All |
| Enrollment | 82 (estimated) |
| Sponsor | Sunnybrook Health Sciences Centre Academic / other |
| Locations | 1 site (Toronto, Ontario) |
| Status | Recruiting |
| Started | November 15, 2026 |
| Main results expected | August 15, 2027 |
| Study ends | December 15, 2027 |
| Registry record updated | November 3, 2026 |
| Trial ID | NCT07913854 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are youths aged 14-19 with a lifetime and/or recent suicidal thoughts, who are English-speaking and regular short-form content consumers.
✕Probably not a fit
Participants with active suicidal intent or recent self-harm may not benefit and may be excluded for safety.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Researchers will recruit youths aged 14-19 with a history of suicidal thoughts or behaviors and randomize them to view suicide-related TikTok content with or without trigger warnings. The trial will measure changes in affect and state anxiety after exposure, helping to understand if warnings influence emotional responses and avoidance. The study is conducted at Sunnybrook Health Sciences Centre in Toronto and aims to clarify whether trigger warnings protect or fail to protect vulnerable youths in social media contexts.
Why it matters
Potential benefit: If trigger warnings are helpful, participants may experience reduced distress when exposed to risky content, contributing to safer social media experiences.
How similar studies have gone: There is limited research on trigger warnings for suicide-related content in clinical populations, making this study relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria:
* Lifetime or recent suicidal thoughts as measured on the Columbia Suicide Severity Rating Scale (C-SSRS)20 screening version. Defined as answering "YES" Question 2 on the C-SSRS with a lifetime and/or past month time-framing ("In your entire life, have you ever had any thoughts of killing yourself?" and/or "In the past month, have you had any thoughts of killing yourself?")
* Self-identified consumer of short-form content on social media (e.g. Instagram reels, TikTok, YouTube Shorts) in the last year.
* English comprehension
Exclusion Criteria:
* Suicidal ideation with any intent or plan in the last 6 months. Defined as answering "YES" on any one C-SSRS Question 3 to 5 with a past 6-months timeframe. Note: Suicidal ideation in the absence of intent or planning is not an exclusion criterion
* Suicidal behaviour in the last 6 months. Defined as answering "YES" to C-SSRS Question 6 ("In your entire life, have you ever done anything, started to do anything, or prepared to do anything to end your life?") AND a 6-months follow up questions ("Was this within the past 6 months?"). Note: Lifetime suicidal behaviour (i.e. answering yes to only Question 6) is not an exclusion criterion
* In active psychosis or mania, as indicated by patient's medical records
Where it's running
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Sunnybrook Health Sciences Center
Toronto, Ontario, Canada Recruiting
Study contacts
- Principal investigator: Rachel Mitchell, MD, MSc — University of Toronto; Sunnybrook Health Sciences Center
- Study coordinator: Zoe Shelton, B.A.
- Email: zoejacklyn.shelton@mail.utoronto.ca
- Phone: 4388703910
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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.