Purpose

Rates of depression increase rapidly during adolescence, especially for girls, and, thus, research is needed to spur the development of novel interventions to prevent adolescent depression. This project seeks to determine if a novel visuocortical probe of affect-biased attention (i.e., steady-state visual evoked potentials derived from EEG) can 1) be used to prospectively predict depression using a multi-wave repeated measures design and 2) modify affect-biased attention and buffer subsequent mood reactivity using real time neurofeedback. This work could ultimately lead to improved identification of adolescents who are at high risk for depression and directly inform the development of mechanistic treatment targets to be used in personalized intervention prescriptions for high-risk youth.

Condition

Eligibility

Eligible Ages
Between 13 Years and 15 Years
Eligible Genders
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Participants will include 90 female adolescents ages 13 years 0 months through 15 years 11 months at study entry.

Exclusion Criteria

  1. Lifetime history of any DSM 5 depressive disorder 2. Lifetime history of taking antidepressants (e.g., SSRIs) 3. Lifetime history of a DSM 5 psychotic, bipolar, or autistic spectrum disorder. 4. Presence of EEG contraindications (e.g., personal lifetime history of seizures or family history of hereditary epilepsy). 5. Being pre-pubertal 6. Lifetime history of a neurological or serious medical condition. 7. Lifetime history of head injury or congenital neurological anomalies (based on parent report). 8. IQ less than 80, as assessed using the Wechsler Abbreviated Scale of Intelligence (WASI). 9. Uncorrected visual disturbance 10. Being acutely suicidal or at risk for harm to self or others.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Basic Science
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Neurofeedback
Participants will receive feedback about their attention to negative distractors during each trial using activity from their brain waves, which will help them reduce their attention to distractors.
  • Other: Neurofeedback
    Participants will receive feedback during a computerized task that is based on their own visuocortical activity evoked by attention to negative distractors and task-relevant stimuli on the computer screen.

Recruiting Locations

More Details

Status
Recruiting
Sponsor
University of Pittsburgh

Study Contact

Mary Woody, PhD
412-383-2143
woodyml@upmc.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.