Clinical trial Recruiting at 1 site Interventional Ages 12 to 17 Women only

How teens' responses to social threat relate to relationships and suicidal thoughts

Official title: Neurocognitive Responses to Social Threat: Links to Day-to-day Connectedness and Suicidality in Adolescent Girls

Run by University of Pittsburgh · NCT07294079 · Data updated 2026-11-12

This study tests whether how girls assigned female at birth ages 12–17 pay attention to social threats relates to their daily relationships and suicidal thoughts or self-harm.

More Suicidal Thoughts and Behaviors trials

Quick facts

Study typeInterventional
Ages12 Years to 17 Years
SexWomen only
Enrollment100 (estimated)
SponsorUniversity of Pittsburgh
Academic / other
Locations1 site (Pittsburgh, Pennsylvania)
StatusRecruiting
StartedJanuary 19, 2026
Main results expectedJune 30, 2030
Study endsAugust 30, 2030
Registry record updatedFebruary 12, 2026
Trial IDNCT07294079 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adolescents assigned female at birth aged 12–17 who have had recurrent suicidal thoughts, suicide-related behaviors, or non-suicidal self-injury in the past year, are medically and neurologically healthy, can read English, and own an iPhone are ideal candidates.

Probably not a fit

Teens who are male or outside the 12–17 age range, have current psychotic disorder, severe substance use disorder, autism spectrum disorder, serious neurological or medical conditions, uncorrected visual impairment, or who do not own an iPhone are not eligible and unlikely to benefit from this protocol.

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

What this trial studies

Researchers will enroll 100 adolescents assigned female at birth, ages 12–17, who have had recent suicidal thoughts, behaviors, or non-suicidal self-injury. Participants complete a baseline clinical interview, a lab visit with EEG while doing a face-memory task that presents angry, sad, happy, and neutral expressions, and daily smartphone surveys plus passive data collection over several weeks. Follow-up questionnaires at 3 and 6 months will track changes in suicidal thoughts and social connectedness to link brain responses to real-world social experience. Text message donation is requested to augment the passive social data.

Why it matters

Potential benefit: If successful, this work could help identify brain and behavior markers that predict which teens are at higher risk, informing earlier, more targeted prevention and support.

How similar studies have gone: Prior research using EEG/ERP and smartphone-based daily surveys has shown promise linking neural responses to social stimuli with real-world emotional states, but applying these methods specifically to predicting adolescent suicidality is still an emerging area.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Between ages 12-17
* Reported recurrent suicidal thoughts and behaviors and/or non-suicidal self-injury within the past year.
* Medically and neurologically healthy, including no evidence of intellectual disability or serious cognitive impairment that would interfere with task performance
* Assigned female at birth
* Willing and able to give informed assent
* Own an iPhone

Exclusion Criteria:

* Unable to read or speak English or cognitive impairment preventing ability to complete assessments
* Lifetime presence of a neurological or serious medical condition
* Lifetime presence of a DSM-5 Autistic Spectrum Disorder
* Current DSM-5 Psychotic Disorder or severe Substance Use Disorder
* Uncorrected visual disturbance (\<20/40 Snellen visual acuity)
* Presence of head injury or congenital neurological anomalies (based on parent report).

Where it's running

  • University of Pittsburgh
    Pittsburgh, Pennsylvania, United States
    Recruiting

Study contacts

  • Principal investigator: Kiera M James, PhD — University of Pittsburgh
  • Study coordinator: Kiera M James, Ph.D.
  • Email: kij9@pitt.edu
  • Phone: 412-634-0004

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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.