Recruiting at 2 sites No phase Post-Traumatic Stress Disorder

Clinical trial for Post-Traumatic Stress Disorder

Official title Disrupting Fear-based Memory Consolidation

ClinicalTrials.gov ID: NCT05560113

What this study is testing

What it's testing
This study is testing whether stopping brain activity right after a scary event can lower fear. It aims to see if this can help prevent PTSD.
Who it's for
You may be able to join if you have had a recent scary or traumatic event.
What's involved
You would get a gentle electric current to your scalp. This happens shortly after you experience a scary memory.
Time commitment
The source text does not say how long the study lasts or how many visits are needed.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 to 65

You may be able to join if

  • Ability to provide informed consent
  • Willingness to participate in study
  • No history of musculoskeletal impairment or neurological disease
  • Clinical diagnosis of PTSD for individuals in the PTSD group.

You likely can't join if

  • Any participant outside the age range
  • Participants that show signs of dementia (score \< 20 on the Montreal Cognitive Assessment)
  • Participants that have a history of major head trauma, a neurodegenerative disorder, or recent (\<6 months) substance abuse;
  • Participants that had a recent history of Central Nervous System (CNS) active drugs that may influence cortical excitability or learning; or
  • Participants that report contraindications to TMS or MRI - if participating in the TMS/MRI experiments
  • Current psychoactive medication usage
See the full eligibility criteria
Who can join
  • Ability to provide informed consent
  • Willingness to participate in study
  • No history of musculoskeletal impairment or neurological disease
  • Clinical diagnosis of PTSD for individuals in the PTSD group.
What rules you out
  • Any participant outside the age range
  • Participants that show signs of dementia (score \< 20 on the Montreal Cognitive Assessment)
  • Participants that have a history of major head trauma, a neurodegenerative disorder, or recent (\<6 months) substance abuse;
  • Participants that had a recent history of Central Nervous System (CNS) active drugs that may influence cortical excitability or learning; or
  • Participants that report contraindications to TMS or MRI - if participating in the TMS/MRI experiments
  • Current psychoactive medication usage
  • Current symptoms of psychosis or bipolar disorder (as indicated by study staff through a clinical interview as part of that study).
  • The study will exclude adults unable to consent, individuals who are not yet adults, pregnant women and prisoners on scientific grounds and to minimize risk.

The study team makes the final eligibility decision.

Where it is enrolling

  • Atlanta, Georgia, United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part, but confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years to 65 years. The study team makes the final eligibility decision.

Where is this trial taking place?

This study is enrolling now at Atlanta, Georgia, United States. Enter your location above to see the nearest enrolling site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool that is independent of the study sponsor. Details come from ClinicalTrials.gov. The study team decides eligibility, and your own doctor gives medical advice.