Clinical trial Recruiting at 2 sites Interventional Ages 11 to 21

Flourish for middle and high school students affected by cyberbullying

Official title: Adaptation and Implementation of Flourish Within Schools: Strengthening Suicide Prevention Services for Adolescents Experiencing Online Victimization

Run by University of Pittsburgh · NCT07506525 · Data updated 2026-11-12

This pilot will test Flourish, a text- and web-based program, to see if it helps middle and high school students who have experienced cyberbullying and are at risk for suicide.

More Suicidal Ideation trials

Quick facts

Study typeInterventional
Ages11 Years to 21 Years
SexAll
Enrollment20 (estimated)
SponsorUniversity of Pittsburgh
Academic / other
Locations2 sites (Bay Village, Ohio and 1 other locations)
StatusRecruiting
StartedMarch 14, 2026
Main results expectedOctober 2026
Study endsJanuary 2027
Registry record updatedApril 1, 2026
Trial IDNCT07506525 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are English-speaking students aged 11–21 with access to a phone or tablet who have experienced cyberbullying and recent suicide risk factors or who are identified by school staff as likely to benefit.

Probably not a fit

Students who cannot meaningfully engage with a text/web program (for example, due to significant cognitive impairment), lack reliable SMS/device access, or require immediate intensive psychiatric care may not benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Flourish is a 4-week automated texting program with an accompanying website that teaches distress tolerance, social problem-solving, and help-seeking skills tailored for youth who have experienced cyberbullying. Middle and high school students (ages 11–21) who report recent cybervictimization and suicide risk factors or are referred by school staff will be onboarded and asked to use Flourish about 2–3 times per week. Participants complete questionnaires and clinical interviews at baseline and follow-ups at 2, 4, and 12 weeks to track psychological distress, suicidal thoughts and behaviors, and social media experiences. The pilot will measure feasibility (≥80% recruitment/retention and weekly use by ≥80% of participants) and change in distress and suicidal ideation over three months, plus exit interviews with school personnel to identify implementation barriers and facilitators.

Why it matters

Potential benefit: If successful, Flourish could reduce psychological distress and suicidal thoughts after cyberbullying and provide a scalable, school-deliverable support option.

How similar studies have gone: Prior digital and text-based adolescent mental health programs have shown mixed but promising results for reducing distress and improving help-seeking, while a targeted cyberbullying-focused program like Flourish is a more novel application.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 11-21 years old
* English-speaking
* have access to a cell phone or tablet that can send/receive SMS text messages
* identified as a student who could benefit from the program by a school staff member - OR - screened eligible based on experiencing cyberbullying and suicide risk factors in the past 3 months
* past 3-month history of cyberbullying assessed by the cybervictimization subscale of the Traditional Bullying and Cyberbullying Victimization Scale and/or presence of online discrimination as measured by a modified measure from the Adolescent Brain and Cognitive Development (ABCD study)
* past 3-month history of suicide risk factors, assessed by: psychological distress (\>13 on the 6-item Kessler Psychological Distress Scale) and/or suicidal ideation or behavior (via the Columbia Suicide Severity Rating Scale)

Exclusion Criteria:

* if a student has a condition that might inhibit their ability to effectively engage with Flourish (e.g., intellectual challenges or low literacy levels)
* if a students' level of acuity would suggest a higher level of care or referral to emergency services
* if a school staff judges the intervention is not appropriate for the student

Where it's running

  • Bay Village School District
    Bay Village, Ohio, United States
    Recruiting
  • University of Pittsburgh
    Pittsburgh, Pennsylvania, United States
    Recruiting

Study contacts

  • Principal investigator: Candice L Biernesser, PhD — University of Pittsburgh
  • Study coordinator: Candice L Biernesser, PhD
  • Email: lubbertcl@upmc.edu
  • Phone: 412-586-9064

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.