UZ Brussel
Brussels, Brussels Capital, 1090, Belgium
NCT Number: NCT07406503
This academic study investigates how MRI-compatible transcranial direct current stimulation (tDCS) over the left dorsolateral prefrontal cortex (DLPFC) influences stress regulation and episodic future thinking in healthy volunteers. Participants undergo one MRI session: combining stress induction, tDCS (real or sham), and functional and metabolic MRI measurements. The study aims to better understand how non-invasive brain stimulation affects the neurophysiological and psychological mechanisms involved in stress processing and future-oriented thinking.
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Notify Me18 year–30 year
All sexes
Interventional
Not applicable
Brussels, Brussels Capital, 1090, Belgium
The purpose of this study is to examine the modulatory effects of non-invasive brain stimulation on cognitive and emotional processes related to stress regulation and episodic future thinking (EFT).
Healthy adult volunteers complete one MRI session. Participants were randomly assigned to active or sham stimulation. First, participants performed an fMRI-based baseline measurement of the EFT task. This task involves imagining specific future personal events in response to cue words presented on a screen and later verbally describing these imagined events outside the scanner.
During the second part, participants complete the Montreal Imaging Stress Task (MIST) - a mental arithmetic paradigm with time pressure and negative feedback to induce acute stress. Immediately afterward, they receive MRI-compatible tDCS (active or sham) for 20 minutes while at rest. The active tDCS delivers 2 mA current through a 4×4 cm anode placed over the left DLPFC and a cathode over the contralateral orbitofrontal region. Sham stimulation follows the same setup with current ramping only at the onset and offset.
Following stimulation, an ASL perfusion scan, MRS spectroscopy targeting the hippocampus, and a post-stimulation EFT fMRI task were conducted. Throughout the MRI scan, behavioral and psychometric data were collected, including questionnaires on rumination, personality, and mood, as well as physiological and biochemical measures such as salivary cortisol and heart rate variability (HRV).
The primary goal is to assess whether active tDCS modulates the neural, endocrine, and behavioral correlates of stress and future-oriented cognition compared to sham stimulation.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
active non-invasive brain stimulation
Sham non-invasive brain stimulation
Time frame: Baseline and immediately post-tDCS (single study visit)
Specificity of episodic future thinking responses assessed using a standardized scoring procedure applied to imagined future events.
Unit of Measure: EFT specificity score (units on a standardized scale)
Time frame: Baseline; immediately post-tDCS; and immediately post-EFT paradigm (single study visit)
Self-reported tension measured using a visual analogue scale (VAS) Unit of Measure:Score on a 0-10 scale. A higher score means more fatigued.
Time frame: Baseline and immediately post-tDCS (single study visit)
Mean blood-oxygen-level-dependent (BOLD) signal change during the episodic future thinking task, averaged across predefined prefrontal-limbic regions of interest.
Unit of Measure: Percent signal change (or beta coefficients from the general linear model)
Time frame: Baseline; immediately post-tDCS; and immediately post-EFT paradigm (single study visit)
Self-reported tension measured using a visual analogue scale (VAS) Unit of Measure: Score on a 0-10 scale. A higher score means more tensed.
Time frame: Baseline; immediately post-tDCS; and immediately post-EFT paradigm (single study visit)
Self-reported vigor measured using a visual analogue scale (VAS). Unit of Measure: Score on a 0-10 scale. A higher score means more vigor.
Time frame: Baseline; immediately post-tDCS; and immediately post-EFT paradigm (single study visit)
Self-reported anger measured using a visual analogue scale (VAS). Unit of Measure: Score on a 0-10 scale. A higher score means more anger.
Time frame: Baseline; immediately post-tDCS; and immediately post-EFT paradigm (single study visit)
Self-reported depressed mood measured using a visual analogue scale (VAS). Unit of Measure: Score on a 0-10 scale. A higher score means more depressed mood.
Time frame: Baseline; immediately post-tDCS; and immediately post-EFT paradigm (single study visit)
Self-reported cheerfulness measured using a visual analogue scale (VAS). Unit of Measure: Score on a 0-10 scale. A higher score means more cheerfulness.
Time frame: Baseline; immediately post-tDCS; and immediately post-EFT paradigm (single study visit)
Self-reported stress measured using a visual analogue scale (VAS).
Unit of Measure: Score on a 0-10 scale. A higher score means more stress.
Time frame: Baseline and immediately post-tDCS (single study visit)
Hippocampal glutamate concentration measured using proton magnetic resonance spectroscopy (¹H-MRS).
Unit of Measure: Institutional units
Time frame: Baseline and immediately post-tDCS (single study visit)
Hippocampal gamma-aminobutyric acid (GABA) concentration measured using proton magnetic resonance spectroscopy (¹H-MRS).
Unit of Measure: Institutional units
Time frame: Baseline and immediately post-tDCS (single study visit)
Hippocampal glutamine concentration measured using proton magnetic resonance spectroscopy (¹H-MRS).
Time frame: Baseline and immediately post-tDCS (single study visit)
Hippocampal N-acetylaspartate (NAA) concentration measured using proton magnetic resonance spectroscopy (¹H-MRS).
Unit of Measure: Institutional units
Time frame: Baseline, immediately post-tDCS, and immediately post-EFT task (single study visit)
Salivary cortisol concentration measured using biochemical assay from saliva samples.
Unit of Measure: nmol/L (or µg/dL)
Time frame: Baseline and Periprocedural (during tDCS)
Cerebral blood flow measured using arterial spin labeling (ASL) MRI. Unit of Measure: mL/100 g/min
Time frame: Baseline (prior to any intervention)
Beck Depression Inventory (BDI-II) The BDI-II consists of 21 items, each scored 0-3. Unit of Measure: BDI-II total score ranging from 0 to 63. Higher scores indicate more depressive symptoms.
Time frame: Baseline (prior to any intervention)
Body mass index calculated from measured body weight and height.
Time frame: Baseline (prior to any intervention)
Trait rumination assessed using the Ruminative Responses Scale (RRS). Unit of Measure: RRS total score (range 22-88; higher scores indicate greater trait rumination).
Time frame: Baseline (single study visit)
Brooding rumination assessed using the Brooding subscale of the Ruminative Responses Scale (BSRI).
Unit of Measure: BSRI (Brooding) subscale score, range 5-20; higher scores indicate greater brooding rumination.
Time frame: Baseline (single study visit)
Trait anxiety assessed using the State-Trait Anxiety Inventory, Trait version (STAI-T).
Unit of Measure: STAI-T total score (range 20-80; higher scores indicate greater trait anxiety).
Universitair Ziekenhuis Brussel
Other
Modulation of the Stressed Brain: Effects of Transcranial Direct Current Stimulation on Stress Regulation and Episodic Future Thinking - an MRI Study in Healthy Volunteers
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