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NCT Number: NCT07527052

Emerging Technologies and Teen Mental Health

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.

Recruiting

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Key information

Age range

12 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

FIU Center for Children and Families

Miami, Florida, 33199, United States

Location status: Recruiting

Location contact

Victor Buitron

CONTACT

[email protected]

305-348-9880

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Prosociality and Agency in Algorithmic Spaces (PAAS) Module

Behavioral

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.

Primary outcomes

  1. Social Disconnection

    Time frame: From immediately before the intervention to immediately following the intervention.

    Two-item self-reported measure of momentary perceived social disconnection.

  2. Perceived Burdensomeness

    Time frame: From immediately before the intervention to immediately following the intervention.

    Two-item self-reported measure of momentary perceived burdensomeness.

Secondary outcomes

  1. 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Victor Buitron

CONTACT

[email protected]

305-348-9880

Sponsors and collaborators

Lead sponsor

Florida International University

Other

Registry information

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Apr 14, 2026
Registry last updated
Apr 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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