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Modulating Stress-Reactivity by Real-Time Multimodal Functional Neuroimaging Based Neurofeedback

University Hospital Basel logo

University Hospital Basel

Status

Withdrawn

Conditions

Pituitary-Adrenal System
Stress

Treatments

Other: Contingent RT-fMRI-NF
Other: Sham RT-fMRI-NF

Study type

Interventional

Funder types

Other

Identifiers

NCT02560233
GRNP_2013S1A2A2035364_1

Details and patient eligibility

About

The overall goal of the outlined study is to establish a Real-Time (RT) functional Magnetic Resonance Imaging (fMRI) Neurofeedback (NF) (RT-fMRI-NF) protocol aiming at modulating neural, endocrine, and subjective reactivity to psychosocial stress.

Full description

The overall goal of the outlined study is to establish an RT-fMRI-NF protocol aiming at modulating neural, endocrine, and subjective reactivity to psychosocial stress. More specifically, the investigators pursue the following goals: a) to evaluate whether neural and subjective stress-reactivity can be modified by training volitional control over targeted brain activity by means of RT-fMRI-NF; b) to evaluate whether neuromodulation by means of RT-fMRI-NF can be used as a new way to modulate hormone-release into the periphery; and c) to evaluate whether the efficacy of neuromodulation by RT-fMRI-NF can also be reflected on EEG data as well as the autonomic nervous system (ANS) measured by heart rate variability (HRV).

Sex

Male

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Sufficient spoken and written knowledge of English
  • Right-handedness
  • Ability to participate in study procedures

Exclusion criteria

  • Present or past psychological or psychiatric therapy
  • Major or unstable general medical conditions
  • Presence of cardiovascular disease
  • Current intake of any medication interfering hormonal assessments
  • History of major cerebral injury
  • Medical MRI contraindication

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

0 participants in 2 patient groups

Contingent
Experimental group
Description:
Contingent RT-fMRI-NF
Treatment:
Other: Contingent RT-fMRI-NF
Non-contingent
Sham Comparator group
Description:
Sham RT-fMRI-NF
Treatment:
Other: Sham RT-fMRI-NF

Trial contacts and locations

1

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Central trial contact

Jong-Hwan Lee, Prof.

Data sourced from clinicaltrials.gov

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