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Acceptability and Feasibility of Apollo in Veterans With a History of PTSD — Apollo PTSD  

PTSD Clinical Trial

Official title:
Acceptability and Feasibility of Apollo Wearable System, Tuned Vibroacoustic Stimulation (TVS) in Veterans With a History of Post-traumatic Stress Disorder (PTSD)

Clinical Trial Summary

The proposed investigation is an open label pilot study intended to establish the acceptability and feasibility of the Apollo in a population of Veterans. Exploratory data regarding biological signatures will also be collected.

Clinical Trial Description

Evaluation of Apollo requires a stepwise process in which initial aims are geared towards identifying biological signatures versus diagnosing, treating, mitigating or curing any conditions. Towards the end of identifying potential biological signatures, we hypothesize the following. 1) Participants who use the Apollo will have an attenuated physiological stress response as measured by improved heart rate variability (HRV) compared to baseline. 2) Participants who use Apollo will have attenuated perceived psychological stress measured by lower scores on psychological correlates of acute stress when compared to baseline ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05019651
Study type Interventional
Source VA Eastern Colorado Health Care System
Contact
Status Completed
Phase Phase 2
Start date February 1, 2022
Completion date June 30, 2023
View Details
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