Non-invasive Nerve Stimulation for PTSD and Sleep

Part of paid clinical trials in Gainesville, Florida.

Sponsor
University of Florida
Study ID
NCT03170440
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - 55 Years
Healthy Volunteers
Accepted

Interventions

  • Transcutaneous nerve stimulation location 1 — DEVICE
    Non-invasive stimulation by transcutaneous electrical nerve stimulation device in test location

Study Details

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

Key Dates

Start date
Nov 1, 2017
Status verified
Jun 2025
Primary completion
Oct 30, 2025
Completion
Oct 30, 2025

Study Design

Enrollment
221 participants (estimated)
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE

Arms

  • Experimental: Noninvasive nerve stimulation type I
    This group will receive one type of nerve stimulation
  • Active Comparator: Noninvasive nerve stimulation type II
    This group will receive second type of nerve stimulation

Primary Outcome Measure

Physiological sleep architectural quality [ Time Frame: up to 8 hours ]

Central Contacts

Locations (3)

FacilityCityStateZIPSite coordinators
UF Health JacksonvilleGainesvilleFlorida32608
Meghan Marotz, MS
904-244-9620
John Williamson, PhD
3523761611
John Williamson, Ph.D. (PRINCIPAL_INVESTIGATOR)
University of FloridaGainesvilleFlorida32610
John Williamson, PhD
352-294-4903
John Williamson, Ph.D. (PRINCIPAL_INVESTIGATOR)
Damon Lamb, Ph.D. (SUB_INVESTIGATOR)
Eric Porges, Ph.D. (SUB_INVESTIGATOR)
Michael Jaffe, M.D. (SUB_INVESTIGATOR)
UF Health JacksonvilleJacksonvilleFlorida32209
Meghan Marotz, MS
904-244-9620

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