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Phase 1 N=157 Randomized Double-blind Treatment

Teen Brain Training (TBT)

Suicide, Attempted · Suicide, Ideation · Depression

Enrolled (actual)
157
Serious AEs
5.7%
Results posted
Mar 2026
Primary outcome: Primary: Columbia Suicide Severity Rating Scale (CSSRS) - Visit 1 — 2.08; 2.37 points

Study Design & Population

Study type
Interventional
Phase
Phase 1
Interventions
neurofeedback training involving dACC (Other); neurofeedback training involving amygdala (Other)
Age
Pediatric, Adult · 11+ yrs
Sex
All
Sponsor
University of Minnesota
Primary completion
Feb 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Columbia Suicide Severity Rating Scale (CSSRS) - Visit 1
2.08; 2.37
PRIMARY
Columbia Suicide Severity Rating Scale (CSSRS) - Visit 4
1.75; 1.77
PRIMARY
Columbia Suicide Severity Rating Scale (CSSRS) - Visit 5
1.17; 1.03
PRIMARY
Suicide Ideation Questionnaire (SIQ) - Visit 1
61.45; 64.27
PRIMARY
Suicide Ideation Questionnaire (SIQ) - Visit 4
52.05; 50.09
PRIMARY
Suicide Ideation Questionnaire (SIQ) - Visit 5
50.13; 47.12
PRIMARY
Neural Target Engagement - Visit 2
0.13; -0.04
PRIMARY
Neural Target Engagement - Visit 3
0.03; 0.079
SECONDARY
Difficulties in Emotion Regulation (DERS) - Visit 1
18.5; 17.71
SECONDARY
Difficulties in Emotion Regulation (DERS) - Visit 2
17.54; 16.89
SECONDARY
Difficulties in Emotion Regulation (DERS) - Visit 3
17.42; 16.47
SECONDARY
Difficulties in Emotion Regulation (DERS) - Visit 4
17.01; 16.3
SECONDARY
Difficulties in Emotion Regulation (DERS) - Visit 5
17.08; 15.73
SECONDARY
Responses to Depression (RD) - Visit 1
54.92; 55.13
SECONDARY
Responses to Depression (RD) - Visit 2
51.35; 49.72
SECONDARY
Responses to Depression (RD) - Visit 3
49.2; 48.37
SECONDARY
Responses to Depression (RD) - Visit 4
50.21; 47.46
SECONDARY
Responses to Depression (RD) - Visit 5
49.32; 43.64
SECONDARY
Children's Depression Rating Scale - Visit 1
46.42; 47.91
SECONDARY
Children's Depression Rating Scale - Visit 4
43.58; 43.36
SECONDARY
Children's Depression Rating Scale - Visit 5
40.57; 38.89

Summary

A non invasive treatment study including participants at risk for suicide attempts and undergoing neurofeedback training. Neurofeedback is controlling your brain activity in real time inside the scanner.

Eligibility Criteria

Inclusion Criteria

  • Adolescents with a history of suicide attempts

Exclusion Criteria

  • Psychotic disorders.
  • Primary substance use disorder.
  • Primary anorexic disorder.
  • Autism Spectrum Disorder.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06183580). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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