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Non-invasive Nerve Stimulation for PTSD and Sleep

NCT03170440 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 221

Last updated 2025-07-01

No results posted yet for this study

Summary

In this study, our objective is to determine the effect of two different nerve stimulation types in changing sleep architecture.

Conditions

Interventions

DEVICE

Transcutaneous nerve stimulation location 1

Non-invasive stimulation by transcutaneous electrical nerve stimulation device in test location

Sponsors & Collaborators

Principal Investigators

  • John Williamson, Ph.D. · University of Florida

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-11-01
Primary Completion
2025-10-30
Completion
2025-10-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03170440 on ClinicalTrials.gov