Sympathetic Overactivity in Post-traumatic Stress Disorder (SO-PTSD)

Mechanisms of Sympathetic Overactivity in Post-traumatic Stress Disorder

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.

Study Overview

• Status: Recruiting
• Conditions: Prehypertension; Post-traumatic Stress Disorder
• Intervention / Treatment: Device: Device-Guided Breathing (DGB); Device: Sham DGB; Device: Transcutaneous Vagal Nerve Stimulation (tVNS); Device: Sham tVNS

Detailed Description

PTSD is highly prevalent in both the military and general population. Because of the tremendous deleterious mental health and socioeconomic impact of PTSD, research to understand and treat all aspects of PTSD is vitally important. One less recognized but highly significant consequence of PTSD is an increased risk of hypertension, cardiovascular disease (CV) disease, and its risk factors. Despite the epidemiologic data demonstrating increased CV risk in PTSD, very little is known about underlying mechanisms. This project will help fill this gap by examining the mechanistic role of sympathetic overactivation in PTSD. Sympathetic hyperactivity has a major role in causing and sustaining hypertension, and contributes to the development of heart failure, arrhythmias, and atherogenesis. Moreover, exaggerated SNS responses during mental stress are associated with an increased risk of hypertension and CV disease.

Slow breathing is an integral part of many ancient meditative practices that are purported to have beneficial physiologic and psychological effects. Clinical applicability of slow breathing requires a method for delivering slow breathing exercises to outpatients on a consistent basis. This can be achieved through device-guided slow breathing (DGB) in which breathing rate is slowed to < 10 breaths/min via an interactive biofeedback device. The RESPeRATE (Intercure, Inc.) device is currently FDA approved for adjunctive treatment of high blood pressure and reduction of stress. This device includes a belt-type respiratory sensor, earbuds to provide audio feedback, and microprocessor that measures adherence and success at achieving slow breathing rates.

Vagal nerve stimulation has been shown in both animal and human studies to safely and effectively reduce sympathetic activity and inflammation. tVNS is a noninvasive method that involves placing a device over the skin overlying the vagus nerve on the neck. The device delivers mild electrical stimulation, using transcutaneous electrical nerve stimulation (TENS) unit. Prior studies have shown that transcutaneous vagal nerve stimulation safely and effectively reduced muscle sympathetic nerve activity in healthy humans and improved heart rate variability, indicating a decrease in sympathetic nervous system (SNS) activity, and a shift in cardiac autonomic function toward parasympathetic (PNS) predominance.

The purpose of this study is to determine if device-guided slow breathing or tVNS improves sympathetic activity and vascular function in persons with PTSD. Participants will be randomized to 15 minutes daily of DGB vs sham-DGB, or tVNS vs. sham-tVNS for 8 weeks.

• Study Type: Interventional
• Enrollment (Estimated): 120
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Deirdre Dixon, MS; Phone Number: 207040 404-321-6111; Email: deirdre.dixon@emory.edu
• Study Contact Backup: Name: Jeanie Park, MD; Phone Number: 207070 404-321-6111

Study Locations

• United States
  • Georgia
    • Decatur, Georgia, United States, 30033
      • Recruiting
      • Atlanta VA Medical Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 65 years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• prehypertensive and normotensive veterans with PTSD, and prehypertensive and normotensive veterans without PTSD (controls)

Exclusion Criteria:

• heart or vascular disease
• illicit drug use within the last 6 months
• excessive alcohol use (>2 drinks per day)
• pregnancy
• autonomic dysfunction
• medications known to affect SNS (clonidine)
• treatment with monoamine oxidase (MAO) inhibitors within the last 14 days
• any serious systemic disease

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

4

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Device-guided Breathing (DGB); Participants randomized to the DGB group use a device to guide their breathing to a slow breathing rate.	Device: Device-Guided Breathing (DGB); The RESPeRATE device will be used for 15 minutes of device-guided breathing daily for 8 weeks. The participant places the elastic belt with a respiration sensor around the upper abdomen, and wears earbuds for audio feedback. The device monitors the breathing rate, calculates inspiration and expiration times, and generates a personalized melody of two distinct ascending and descending tones for inhalation versus exhalation. Users effortlessly entrain their breathing pattern with the tones, and the device gradually guides the user to a prolonged expiration time and slower respiratory rate (to < 10 breaths/minute). The device automatically stores usage data, allowing for quantification of adherence and performance.; Other Names: RESPeRATE
Sham Comparator: Sham DGB; Participants randomized to the sham DGB group use a device identical to the DGB device but respiratory rates are not guided lower than the physiological rate.	Device: Sham DGB; The sham device is identical to the DGB device, except it does not guide respiratory rates to slow down and instead maintains a rate of 14 breaths per minute. The sham device is used for 15 minutes per day for 8 weeks.
Experimental: Transcutaneous Vagal Nerve Stimulation (tVNS); Participants randomized to use a tVNS device to deliver mild electrical stimulation to the vagal nerve.	Device: Transcutaneous Vagal Nerve Stimulation (tVNS); tVNS is a noninvasive method that involves placing a device over the skin overlying the vagus nerve on the neck. The device delivers mild electrical stimulation, using transcutaneous electrical nerve stimulation (TENS) unit. The stimulation is increased until there is a vibration and slight muscle contraction in the lower face or neck. Then the stimulation is delivered for 2 minutes on the left side of the neck, and on the right side of the neck, for a total of 4 minutes. The tVNS device is used twice daily for 8 weeks.; Other Names: gammaCore
Sham Comparator: Sham tVNS; Participants randomized to use the sham tVNS device which vibrates but does not stimulate the vagal nerve.	Device: Sham tVNS; Sham stimulation is delivered using a device that is identical to the gammaCore device but is programed to deliver a lower frequency that can be felt by the participant but does not actually stimulate the vagus nerve. The sham device is used twice daily for 8 weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Muscle Sympathetic Nerve Activity (MSNA) Burst Frequency at Rest	MSNA is assessed with microneurography where a tungsten microelectrode inserted in the nerve records sympathetic nerve activity.	Baseline, Week 8
Change in Baroreflex Sensitivity (BRS) at Rest	Arterial baroreflex sensitivity (BRS) will be tested using pharmacologic manipulation of blood pressure at rest. BRS is assessed by measuring changes in MSNA and heart rate during arterial blood pressure changes induced by nitroprusside and phenylephrine.	Baseline, Week 8
Change in MSNA Burst Frequency While Under Mental Stress	Mental stress will be induced by having participants complete mental arithmetic and with a combat virtual reality clip.	Baseline, Week 8
Change in BRS While Under Mental Stress	Mental stress will be induced by having participants complete mental arithmetic and with a combat virtual reality clip. Arterial baroreflex sensitivity (BRS) will be tested using pharmacologic manipulation of blood pressure at rest and during mental stress.	Baseline, Week 8

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Endothelial Function	Endothelial Function will be measured using peripheral arterial tonometry.	Baseline, Week 8
Vascular Stiffness	Vascular stiffness will be measured noninvasively using pulse wave analysis and pulse wave velocity.	Baseline, Week 8

Collaborators and Investigators

• Sponsor: Emory University
• Collaborators: US Department of Veterans Affairs
• Investigators: Principal Investigator: Jeanie Park, MD, Emory University and the Atlanta VA Medical Center

Publications and helpful links

General Publications

• Fonkoue IT, Hu Y, Jones T, Vemulapalli M, Sprick JD, Rothbaum B, Park J. Eight weeks of device-guided slow breathing decreases sympathetic nervous reactivity to stress in posttraumatic stress disorder. Am J Physiol Regul Integr Comp Physiol. 2020 Oct 1;319(4):R466-R475. doi: 10.1152/ajpregu.00079.2020. Epub 2020 Aug 26.

Study record dates

Study Major Dates

• Study Start (Actual): July 1, 2012
• Primary Completion (Estimated): December 1, 2027
• Study Completion (Estimated): December 1, 2027

Study Registration Dates

• First Submitted: June 21, 2012
• First Submitted That Met QC Criteria: June 22, 2012
• First Posted (Estimated): June 25, 2012

Study Record Updates

• Last Update Posted (Estimated): January 15, 2026
• Last Update Submitted That Met QC Criteria: January 13, 2026
• Last Verified: January 1, 2026

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Trauma and Stressor Related Disorders; Vascular Diseases; Cardiovascular Diseases; Mental Disorders; Stress Disorders, Traumatic; Stress Disorders, Post-Traumatic; Prehypertension
• Other Study ID Numbers: IRB00054697; 2025P011325 (Other Identifier: Emory IRB)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

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