Parent-Adolescent Training on Neurofeedback and Synchrony

Completed · Not applicable

Conditions studied: Testing Protocol With Healthy Individuals for Feasibility

In brief

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.

Key facts

Study ID

NCT03929263

Run by

Oklahoma State University Center for Health Sciences

People needed

24

Starts

2019-09-25

Expected to finish

2021-02-27

Last updated by the study team

2024-09-24

Who can join

Age: 13 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Eligible for fMRI
• Sufficient English fluency to complete tasks
• BMI ≦ 40.0
• Right-handed
• Biological female
• Co-residing at least 4 days/week
• Adult participants: Biological mother of adolescent participant
• Adult participants:Primary caregiver > 50% of child's lifespan
• Adult participants:BMI ≧ 18.0
• Adolescent participants: Age 13-17 years
• Adolescent participants: BMI ≧ 16.0

You may not qualify if…

• Current psychiatric diagnosis
• Medications influencing fMRI
• Medical conditions influencing fMRI
• Alcohol or psychoactive drug on scan day
• Adolescent participants: Neurodevelopmental delay
• Adolescent participants: History of mood or psychotic disorder
• Adolescent participants: History of obsessive-compulsive disorder (OCD) or attention-deficit/hyperactivity disorder (ADHD)

Where it is running

• Laureate Institute for Brain Research — Tulsa, Oklahoma, United States

Full record on ClinicalTrials.gov

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