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Emerging Technologies and Teen Mental Health

Emerging Technologies and Teen Mental Health

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07527052
Enrollment
200
Registered
2026-04-14
Start date
2026-03-20
Completion date
2028-12-01
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Emotional Distress, Social Functioning, Suicidal Ideation

Brief summary

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.

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.

Interventions

BEHAVIORALProsociality and Agency in Algorithmic Spaces (PAAS) Module

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.

Sponsors

Florida International University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 17 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Social DisconnectionFrom immediately before the intervention to immediately following the intervention.Two-item self-reported measure of momentary perceived social disconnection.
Perceived BurdensomenessFrom immediately before the intervention to immediately following the intervention.Two-item self-reported measure of momentary perceived burdensomeness.

Secondary

MeasureTime frameDescription
Subjective Units of Distress Scale (SUDS)From immediately prior to the intervention to immediately following the intervention.A self-reported sliding scale of momentary distress 0-10 numeric anchors.

Countries

United States

Contacts

CONTACTVictor Buitron
vbuitron@fiu.edu305-348-9880

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 15, 2026