Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
Healthy Volunteers
ID05895006

Intrinsic and Novelty-related Sensory Cortical Disinhibition and Sensory-Prefrontal-Cortex-Amygdala Pathology in Posttraumatic Stress Disorder (PTSD) Using Transcranial Alternating Current Stimulation (tACS) and Transcranial Random Noise Stimulation (tRNS)

Led by The University of Texas Health Science Center, Houston · Updated on 2025-09-12

160

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

T

The University of Texas Health Science Center, Houston

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating the brain mechanisms behind Posttraumatic Stress Disorder (PTSD), focusing on how abnormal activity in sensory and brain regions relates to symptoms like anxiety and hypervigilance. The study aims to test a new model linking sensory cortex, prefrontal cortex, and amygdala dysfunctions to better understand PTSD's underlying causes. It also evaluates how a brain stimulation technique called Transcranial Alternating Current Stimulation (tACS) may influence these brain networks and emotional responses. Participants will be randomly assigned to one of three groups: active tACS at their individual alpha frequency, a sham (placebo) tACS where no current is passed, or an active control using Transcranial Random Noise Stimulation (tRNS). Each stimulation involves placing electrodes on the scalp within an EEG cap and delivering a weak electrical current for 10 to 40 minutes. The study includes two experiments using simultaneous EEG and functional MRI scans, taken before and after stimulation during rest and a novelty detection task. During the study, participants will undergo brain imaging and EEG recordings to measure changes in brain activity and responses related to attention and vigilance. These include monitoring EEG alpha power, fMRI blood flow signals, performance on an oddball detection task, and skin conductance. The researchers will compare these measures before and immediately after stimulation to assess the effects. Participant involvement lasts during the study sessions, and the safety and effects of the brain stimulation are closely monitored throughout the process.

CONDITIONS

Brief Title

A Neurosensory Account of Anxiety and Stress (Study 1)

Who Can Participate

Age: 18Years - 50Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Right-handed
  • Normal or corrected-to-normal vision and normal sense of smell
  • Age between 18 and 50 years
  • Meet tACS screening criteria, including no serious head injury or loss of consciousness
  • Diagnosis of PTSD for patients
  • Stable psychotropic medication use for at least 2 months if applicable
  • Abstain from substance use 48 hours before the experiment if mild substance use disorder or occasional use
Not Eligible

You will not qualify if you...

  • History of major medical illnesses such as cancer, metabolic syndrome, cardiovascular disease, or inflammatory disorders
  • History of neurological disorders like seizures, stroke, or Parkinson's disease
  • Patients with concurrent Axis I diagnoses except depression, anxiety, or mild substance use disorder
  • Healthy controls with any DSM-5 Axis I disorder or current psychoactive medication use
  • Severe psychiatric instability or active suicidal/homicidal behavior
  • History of head trauma with unconsciousness over 5 minutes
  • Regular consumption of 3 or more alcoholic beverages daily
  • Inability to abstain from substance or sleep medication use 48 hours before scanning
  • Use of calcium channel blockers or alpha-blockers without ability to stop 48 hours prior
  • Failed urine drug screening
  • Pregnancy
  • Presence of electrically, magnetically, or mechanically activated implants such as pacemakers

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Single session lasting approximately 10 to 40 minutes of stimulation plus setup and assessments.

Participants receive transcranial electrical stimulation via an EEG cap combined with simultaneous EEG-fMRI recordings during resting state and a novelty task before and after stimulation.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

The University of Texas Health Science Center at Houston

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

W

Wen Li, PhD

J

Jada Malveaux, MA

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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