Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT01627301

Sympathetic Overactivity in Post-traumatic Stress Disorder

Led by Emory University · Updated on 2026-01-15

120

Participants Needed

1

Research Sites

804 weeks

Total Duration

On this page

Sponsors

E

Emory University

Lead Sponsor

U

US Department of Veterans Affairs

Collaborating Sponsor

AI-Summary

What this Trial Is About

Post-traumatic stress disorder (PTSD) is a highly prevalent anxiety disorder that is associated with an increased risk of cardiovascular (CV) disease and hypertension. One potential mechanism is overactivation of the sympathetic nervous system (SNS), both at rest and particularly during stress. This study will evaluate whether 8 weeks of daily DGB therapy or transcutaneous vagus nerve stimulation (tVNS) therapy improves SNS activity at rest and during stress.

CONDITIONS

Official Title

Sympathetic Overactivity in Post-traumatic Stress Disorder

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants must be prehypertensive or have normal blood pressure
  • Veterans with or without PTSD can participate
  • Age between 18 and 65 years
Not Eligible

You will not qualify if you...

  • Presence of heart or vascular disease
  • Illicit drug use within the last 6 months
  • Excessive alcohol use (more than 2 drinks per day)
  • Pregnancy
  • Autonomic dysfunction
  • Use of medications known to affect the sympathetic nervous system, such as clonidine
  • Treatment with monoamine oxidase (MAO) inhibitors within the last 14 days
  • Any serious systemic disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Atlanta VA Medical Center

Decatur, Georgia, United States, 30033

Actively Recruiting

Loading map...

Research Team

D

Deirdre Dixon, MS

CONTACT

J

Jeanie Park, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here