Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
NCT06874595

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

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Virginia Commonwealth University

Richmond, Virginia, United States, 23298

Actively Recruiting

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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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