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NCT Number: NCT07364084

Real-time Neurofeedback Training of the Medial Prefrontal Cortex Based on Imagined Social Support

Randomized active-sham controlled between-subject real-time fMRI neurofeedback trial aiming to modulate activity in the medial prefrontal cortex (mPFC) to improve subjective negative anticipation.

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Key information

Conditions

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Electronic Science and Technology of China(UESTC), Chengdu, Sichuan 611731

Chengdu, Sichuan, 611731, China

Location status: Recruiting

Location contact

Benjamin Becker, Dr

CONTACT

[email protected]

86-28-61830670

About this study

A double-blinded, placebo-controlled, between-subject design will be employed in this study. In a randomized order, a total of 60 healthy subjects will be recruited and assigned to the experimental group (EG; N=30), which receives real feedback from the medial prefrontal cortex (mPFC), or the sham control group (CG; N=30) which receives sham feedback from an unrelated brain region. Neurofeedback training consists of 1 baseline session without feedback (also as a localizer task), 4 training sessions with intermittent feedback and 1 transfer session without feedback. Each NF run includes 5 regulation blocks and 5 baseline blocks. Each trial starts with a jittered fixation cross (2~8 s), a modulation block (i.e. regulation or baseline; 30 s) without continous feedback, and a intermittent feedback period (4s) to display the mean activiation of the mPFC/control region during the regulation block compared with baseline block. Objectives are to determine (1) if subjects in the neurofeedback (NF) group can gain volitional control over the mPFC activation using imagined social support as regulation strategy, (2) whether successful increased modulation of the mPFC could improve negative anticipation and sense of control for future events .

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • -Healthy subjects without any past or present psychiatric or neurological disorders

Exclusion criteria

  • History of brain injury
  • Psychiatric or Neurological Disorder
  • Contraindications for MRI
  • Regular use of psychotropic substances (medication, drugs)

Treatment and study plan

real-time fMRI sham-controlled neurofeedback training procedure

Procedure

real-time fMRI neurofeedback training procedure running on the Turbo Brain voyager (TBV) 4.2 software (Brain Innovation, Maastricht, The Netherlands)

Primary outcomes

  1. Neural activity of the medial prefrontal cortex (mPFC) based on blood oxygen level-dependent (BOLD) signal

    Time frame: 1 hour

    Training-induced changes in mPFC activity will be assessed by analyzing BOLD-level activation of the mPFC

Secondary outcomes

  1. Training-related changes in anticipated anxiety

    Time frame: 1 hour

    Participants will be required to rate the anticipated anxiety of future events using a Likert Scale ranging from 1 to 9 (1 = not at all anxious) and 9 = very anxious).

Study contacts

Contact information is provided by the study sponsor or research team.

Benjamin Becker, Dr

CONTACT

[email protected]

86-28-61830670

Sponsors and collaborators

Lead sponsor

University of Electronic Science and Technology of China

Other

Registry information

Official study title

Self-modulation of the mPFC Using Rt-fMRI NF Training to Improve Negative Anticipation for Future Events

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jan 23, 2026
Registry last updated
Jan 28, 2026

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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