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Completed

NCT Number: NCT00729547

The Therapeutic Efficacy of Neurofeedback in Depression

The investigators examined the therapeutic efficacy of neurofeedback in depression subjects. The investigators hypothesize that 5 weeks neurofeedback training will be able to alleviate depressive symptoms.

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Key information

Age range

20 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Oriental Neuropsychiatry, Kyunghee Medical Center

Seoul, 130-702, South Korea

About this study

Subject

  • Fulfilled DSM-IV criteria for depressive disorders.
  • Persons who had organic disorders were excluded.
  • Who had been treated by psychoactive drugs for at least 2 months prior to the study were excluded.

Design

  • Subjects were randomly assigned to two groups (EEG biofeedback /psychotherapy placebo) by block randomization.
  • EEG biofeedback training was provided for 5 weeks(10 sessions, twice per week). Each training session was composed of 6 four minute trials followed by 5 thirty second rest periods
  • Psychotherapy placebo session was provided for 5 weeks. These sessions consisted of additional assessment, interpretation of the test results and providing information on course and treatment of mood disorder.
  • After subjects completed the training, they participated in a month-long (twice per week) self-training session to maintain a similar mental state during neurofeedback training sessions without feedback system's assistance.
  • Subjects who had finished the psychotherapy placebo were referred to other therapists as necessary.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • clinical diagnosis of mood disorder
  • right handed
  • current BDI-2 score exceed 10

Exclusion criteria

  • with psychotic symptom
  • with organic disorders
  • treated by psychoactive drugs for at least 2 months prior to the study
  • history of pathologic alcohol use

Treatment and study plan

Neurofeedback

Behavioral

enhance relative activity level of left frontal activity

Other names: Asymmetry training

Psychotherapy placebo

Behavioral

These sessions consisted of additional assessment, interpretation of the test results and providing information on course and treatment of mood disorder.

Primary outcomes

  1. frontal EEG asymmetry indexes

    Time frame: 5 weeks

Secondary outcomes

  1. BDI-2

    Time frame: 5 weeks

Sponsors and collaborators

Lead sponsor

Korea University

Other

Collaborators

  • Korea Research Foundation
  • Kyunghee University

Registry information

Official study title

The Therapeutic Efficacy of Frontal EEG Asymmetry Neurofeedback in Depression

Acronym: neurofeedback

Important dates

Study start
2006
Primary completion
2006
Study completion
2007
First posted
Aug 7, 2008
Registry last updated
Aug 7, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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