Actively Recruiting
Psychobiological Responses Following Exercise and Brain Stimulation
Led by Virginia Commonwealth University · Updated on 2026-03-16
29
Participants Needed
1
Research Sites
97 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Psychobiological Responses Following Exercise and Brain Stimulation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy adults
- Aged 18 to 50 years
- Consent to participate and complete a Physical Activity Readiness Questionnaire (PAR-Q)
- Free from any neurological or psychiatric disorder
- Not taking any medication that affects the central nervous system
- No contraindications for HD-tDCS, including no metal implants in the head, pacemaker, medical bumps, seizures, or scalp/head lesions
- No contraindications for bioelectrical impedance, such as electronic medical implants or limb amputation
- Not regular users of tobacco products (cigarettes, cigars, chewing tobacco)
- Consume fewer than ten alcoholic beverages per week
You will not qualify if you...
- Do not meet the PAR-Q screening criteria for participation in moderate physical activity
- Women who are pregnant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Virginia Commonwealth University
Richmond, Virginia, United States, 23298
Actively Recruiting
Research Team
E
Edmund Acevedo
CONTACT
M
Monique Morton
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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