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A Trial of Neurofeedback as an Adjunctive Treatment for Youth in Outpatient Mental Health Settings

A Trial of Neurofeedback as an Adjunctive Treatment for Youth in Outpatient Mental Health Settings

Recruiting
6-12 years
All
Phase N/A

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Overview

The purpose of this study is to test the feasibility and effectiveness of a neurofeedback intervention conducted as an adjunctive behavioral health treatment to reduce trauma and affective symptoms in trauma-exposed youth.

Eligibility

Inclusion Criteria:

(children)

  • caregiver-reported exposure to two or more ACE types on the ACE-Q-Child measure.
  • ages of 6-12 years old
  • receiving or eligible to receive trauma-focused cognitive behavior therapy or another type of trauma-focused therapy, as determined by their primary therapist, designated as the TAU condition
  • speaks and reads English

(caregivers)

  • own an iPhone, iPad, smartphone, or tablet that is equipped with Bluetooth and uses an Apple or Android operating system that is compatible with the MUSE Calm app and accompanying MUSE wearable neurofeedback device
  • speaks and read English

Exclusion Criteria:

Child-caregiver dyads will be excluded if

  • the child falls outside of the required age range,
  • has a documented history of epilepsy
  • is currently considered to be at high risk for suicide attempt
  • is currently experiencing psychosis

Study details
    Trauma

NCT04871009

University of Rochester

27 January 2024

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FAQs

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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