MedTrace Logo

Parent-Adolescent Training on Neurofeedback and Synchrony

NCT03929263 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2024-09-24

Study results available
· View outcomes & findings →

Summary

The study will test a real-time functional magnetic resonance imaging (fMRI) hyperscanning neurofeedback protocol for feasibility with ten mothers and their psychiatrically healthy adolescent daughters, with the eventual goal to test this in a sample of depressed adolescents in a future study.

Conditions

  • Testing Protocol With Healthy Individuals for Feasibility

Interventions

BEHAVIORAL

Real-time fMRI neurofeedback

Participants will attempt to regulate own and/or their partner's brain activation in a specified brain region via real-time fMRI neurofeedback.

Sponsors & Collaborators

  • Oklahoma State University

    collaborator OTHER

  • Oklahoma State University Center for Health Sciences

    lead OTHER

Principal Investigators

  • Kara L Kerr, PhD · Oklahoma State University

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
13 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-09-25
Primary Completion
2021-02-27
Completion
2021-02-27

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03929263 on ClinicalTrials.gov