- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07527052
Emerging Technologies and Teen Mental Health
April 8, 2026 updated by: Florida International University
This study will recruit teens who are experiencing subacute suicidal ideation to test the effect of a brief psychoeducational intervention focused on social media use wherein youth learn about active and prosocial use of social media platforms.
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
This study seeks to test a brief psychoeducational intervention among teens between the ages of 12-17 who experience subacute suicidal ideation (i.e.
suicidal ideation which does not necessitate intensive, restrictive services) .
Participants will be youth recruited from clinic-referred families and the community at large, as part of ongoing recruitment at the FIU Center for Children and Families.
Families interested in the study will complete a screening process, and eligible participants will then provide consent (from parents) and assent (from youth) before beginning the study.
The brief psychoeducational intervention will focus on social media use wherein youth learn about active and prosocial use of social media platforms.
Study Type
Interventional
Enrollment (Estimated)
200
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Victor Buitron
- Phone Number: 305-348-9880
- Email: vbuitron@fiu.edu
Study Locations
-
-
Florida
-
Miami, Florida, United States, 33199
- Recruiting
- FIU Center for Children and Families
-
Contact:
- Victor Buitron
- Phone Number: 305-348-9880
- Email: vbuitron@fiu.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Adolescents must (A) be between ages 12 and 17 years
- (B) have a positive screen for suicide risk (i.e. endorsement of suicidal ideation via self-report or parent-report)
- (C) have access to a personal social media account
- (D) be fluent in English
- (E) have available a parent who is fluent in English or Spanish.
Exclusion Criteria:
- Adolescents must not (A) have cognitive impairment or developmental delay which does not allow for the completion of basic study procedures (i.e., reading and filling out questionnaires; talking to a clinician)
- (B) show imminent risk or a history of hurting themselves or others requiring intensive and restrictive services.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Prosociality and Agency in Algorithmic Spaces (PAAS) Module
This arm involves the administration of the PAAS module in a single 30-minute session conducted remotely.
|
This intervention involves brief psychoeducation designed to increase algorithmic literacy and encourage prosocial social media engagement.
Specifically, a study staff member will discuss with youth how online algorithmic content (e.g., scrollable social media feeds) is shaped by user inputs and platform goals, and will be guided to engage with content related to prosocial topics and engagement.
Working collaboratively with the administrator, participants will modify their algorithmic inputs (e.g., likes, searches, follows) in vivo and observe immediate changes in their feed, if any.
Parents will receive a handout explaining the topics covered in the psychoeducational session.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Social Disconnection
Time Frame: From immediately before the intervention to immediately following the intervention.
|
Two-item self-reported measure of momentary perceived social disconnection.
|
From immediately before the intervention to immediately following the intervention.
|
|
Perceived Burdensomeness
Time Frame: From immediately before the intervention to immediately following the intervention.
|
Two-item self-reported measure of momentary perceived burdensomeness.
|
From immediately before the intervention to immediately following the intervention.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Subjective Units of Distress Scale (SUDS)
Time Frame: From immediately prior to the intervention to immediately following the intervention.
|
A self-reported sliding scale of momentary distress 0-10 numeric anchors.
|
From immediately prior to the intervention to immediately following the intervention.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 20, 2026
Primary Completion (Estimated)
December 1, 2028
Study Completion (Estimated)
December 1, 2028
Study Registration Dates
First Submitted
April 8, 2026
First Submitted That Met QC Criteria
April 8, 2026
First Posted (Actual)
April 14, 2026
Study Record Updates
Last Update Posted (Actual)
April 14, 2026
Last Update Submitted That Met QC Criteria
April 8, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB-25-0588
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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