- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06874595
Psychobiological Responses Following Exercise and Brain Stimulation
March 12, 2026 updated by: Virginia Commonwealth University
Anxiety disorders are the most common mental health diagnosis in the US; 19.1% of U.S. adults (23.4% for females and 14.3% for males).
In addition, the Global Burden of Disease study (2010) found that anxiety disorders were the sixth leading cause of disability (years of life lived with disability).
These debilitating disorders are characterized by excessive worry and fear about everyday situations, and physical symptoms including restlessness, being easily fatigued, difficulty concentrating, irritability, muscle tension, or sleep disturbance.
Furthermore, anxiety is linked to other mental disorders including depression and substance abuse; is associated with cardiovascular disease risk factors and a higher rate of cardiovascular disease; and is related to premature mortality.
These data have led to the investigation of a breadth of plausible treatments for anxiety, including medications and psychotherapy.
However, likely due to the breadth of complex mechanisms involved in the pathophysiology of anxiety disorders and the unfavorable side effects of various medications, a considerable number of individuals do not have a satisfactory response to these treatments.
This has led investigators to examine plausible novel interventions to alleviate anxiety and its symptoms.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
- Other: Cycling exercise at 65% of HRR for 20 minutes followed by HD-tDCS (exercise + HD-tDCS)
- Other: Cycling exercise at 65% of HRR exercise followed by sham HD-tDCS (exercise + sham tDCS)
- Other: No exercise followed by HD-tDCS (no exercise + HD-tDCS).
- Other: State Anxiety Inventory
- Other: Visual Analog Scale for Anxiety
Detailed Description
Transcranial direct current stimulation (tDCS), a non-invasive central neuromodulatory technique that is inexpensive and safe, has been utilized to stimulate specific regions of the brain and has demonstrated promising results for alleviating anxiety and depression.
(1) evidence supports the administration of anodal stimulation over the left dorsolateral prefrontal cortex (DLPFC) to excite neuronal activity and cathodal stimulation over the right DLPFC to inhibit activity (a bicephalic tDCS montage with 2 mA of stimulation at the left DLPFC) as the most effective tDCS treatment to alleviate anxiety in humans and (2) that "tDCS may be more effective when used in combination with drugs and cognitive behavioral therapies".
However, results from studies that have examined the neurophysiological and behavioral effects of tDCS are not consistent.
This is likely because the highest cortical current density may not have occurred directly under the target electrode, thus altering the effects of tDCS.
High-density tDCS (HD-tDCS) is similar to conventional tDCS utilizing anode and cathode placement on the scalp to produce unidirectional current flow, however, to enhance precision and accuracy, HD-tDCS utilizes smaller electrodes and most often in a "4X1 ring" montage (center anode electrode surrounded by four return cathode electrodes).
This HD-tDCS montage delivers a precise current to the intended target site and has been found to be well tolerated and safe for healthy humans.
Furthermore, the utilization of HD-tDCS can facilitate the elucidation of mechanisms of action that can provide greater clarity regarding discrepant results in the literature and for considering future advancements in enhancing effective HD-tDCS implementation strategies.
HD-tDCS stimulation increases the membrane potential by several millivolts without triggering an action potential.
Study Type
Interventional
Enrollment (Estimated)
29
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Edmund Acevedo
- Phone Number: (804) 814-4355
- Email: eoacevedo@vcu.edu
Study Contact Backup
- Name: Monique Morton
- Phone Number: 804-828-1948
- Email: mortonmy@vcu.edu
Study Locations
-
-
Virginia
-
Richmond, Virginia, United States, 23298
- Recruiting
- Virginia Commonwealth University
-
Contact:
- Edmund Acevedo, PhD
- Phone Number: 804-828-1948
- Email: eoacevedo@vcu.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Healthy adults
- aged 18 to 50
- consent and complete a Physical Activity Readiness Questionnaire (PAR-Q)
- be free from any neurological or psychiatric disorder
- not be taking any medication that could affect the central nervous system
- not have any contraindication for HD-tDCS (i.e. not having metal implanted in the head, pacemaker, medical bumps, seizures, lesions on the scalp or head ) or for bioelectrical impedance (i.e., electronic medical implant, such as a pacemaker or implantable cardioverter defibrillator, and limb amputation)
- not be regular users of tobacco products (cigarettes, cigars, chewing tobacco)
- not consume an average of more than ten alcoholic beverages per week
Exclusion Criteria:
- Individuals who do not meet the PAR-Q screening criteria for participation in moderate physical activity will be excluded from participating in this study
- women who are pregnant will be exclude from this study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: High density transcranial direct current stimulation (HD-tDCS)
HD-tDCS (High-definition transcranial direct current stimulation) is a novel non-invasive brain stimulation (NIBS) technique based on the principle that when weak intensity electric currents are targeted on specific areas of the scalp, they cause underlying cortical stimulation.
|
Subject will complete a Cycling exercise at 65% of HRR for 20 minutes and then a High-definition transcranial direct current stimulation (HD-tDCS) is a non-invasive brain stimulation technique that uses small electrodes to deliver weak electric currents to the scale.
Transcranial direct current stimulation (tDCS) uses weak direct currents of the order of 0.5 mA to 4 mA to modulate cortical activity by exciting or suppressing underlying neurons.
Subject will complete a Cycling exercise at 65% of HRR for 20 minutes and then a sham High-definition transcranial direct current stimulation (HD-tDCS) is a non-invasive brain stimulation technique that uses small electrodes to deliver weak electric currents to the scale.
Transcranial direct current stimulation (tDCS) uses weak direct currents of the order of 0.5 mA to 4 mA to modulate cortical activity by exciting or suppressing underlying neurons.
No exercise but a High-definition transcranial direct current stimulation (HD-tDCS) is a non-invasive brain stimulation technique that uses small electrodes to deliver weak electric currents to the scale.
Transcranial direct current stimulation (tDCS) uses weak direct currents of the order of 0.5 mA to 4 mA to modulate cortical activity by exciting or suppressing underlying neurons.
A widely used psychological assessment tool designed to measure both state and trait anxiety.
40 self-report items rated on a 4-point Likert scale (1 = "Almost Never" to 4 = "Almost Always").
Higher scores indicate higher levels of anxiety.
Scores are compared to normative data to determine if they fall within the range of typical or clinical anxiety.
The Visual Analogue Scale for Anxiety (VASA) is a 100-millimeter line that helps people measure how anxious they feel.
The scale has a mark on the left end that indicates "not at all anxious" and a mark on the right end that indicates "very anxious".
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Examine the anxiolytic effects of high density transcranial direct current stimulation (HD-tDCS) "primed" with physical activity (PA)
Time Frame: Completion of 4 visits to research laboratory up to 15 days
|
Physical activity prior to HD-tDCS will enhance the anxiolytic effects beyond the benefits of physical activity alone and HD-tDCS alone.
Thus, demonstrating a priming effect of PA on the anxiety alleviating electrical pathways that HD-tDCS activates at subthreshold level.
Visual Analog Scale for Anxiety (VAS-Anxiety; rating from 0 = "not at all anxious" to 100 = "the most anxious I have ever felt") and three other scales assessing tingling, stiffness and numbness will be administered with a similar VAS
|
Completion of 4 visits to research laboratory up to 15 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cerebral hemodynamics assessment
Time Frame: Completion of 4 visits to research laboratory up to 15 days
|
Cerebral hemodynamics will be assessed utilizing a Portalite near-infrared spectroscopy (NIRS) device .
Changes in cerebral hemodynamics are strongly correlated, both spatially and temporally, with changes in neural activity.
The Portalite NIRS system utilizes near-infrared light, which penetrates the skull and brain but is absorbed by hemoglobin (Hb) chromophores in capillary, arteriolar, and venular beds
|
Completion of 4 visits to research laboratory up to 15 days
|
|
HRV parameters will be acquired and calculated
Time Frame: Completion of 4 visits to research laboratory up to 15 days
|
IHRV parameters will be calculated using the HRV analysis function included in the Biopac AcqKnowledge software.
The root mean square of successive differences between normal heartbeats (RMSSD) is obtained by calculating each successive time difference between heartbeats in milliseconds.
Then, each of the values is squared and the result is averaged before the square root of the total is obtained.
The RMSSD reflects the beat-to-beat variance in HR and is the primary time-domain measure used to estimate the vagally mediated changes reflected in HRV.
In addition, low frequency (LF) and high frequency (HF) HRV parameters will be computed in absolute power (ms2).
High frequency (HF: 0.15-0.4
Hz) is associated with parasympathetic activity and low frequency (LF: 0.04 - 0.15 Hz) is related to both parasympathetic and sympathetic activity, as it may represent baroreflex-mediated autonomic nervous system (ANS) modulation.
|
Completion of 4 visits to research laboratory up to 15 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Edmund Acevedo, Virginia Commonwealth University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 19, 2025
Primary Completion (Estimated)
February 1, 2027
Study Completion (Estimated)
February 1, 2027
Study Registration Dates
First Submitted
February 4, 2025
First Submitted That Met QC Criteria
March 7, 2025
First Posted (Actual)
March 13, 2025
Study Record Updates
Last Update Posted (Actual)
March 16, 2026
Last Update Submitted That Met QC Criteria
March 12, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HM20031307
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
Yes
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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