Post Traumatic Stress Disorder Clinical Trials
68 studies are recruiting for post traumatic stress disorder in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies, page 2
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Exploring Virtual Reality Adventure Training Exergaming
The current project aims to design and implement an 8-week Virtual Reality Adventure Therapy Exergaming (V-RATE) intervention focused on women veterans. A randomized controlled trial using a repeated measure design with a 1-month follow-up assessment will be employed to examine effects on physical …
- Stage
- Not phased
- Ages
- 18 to 45
- Site
- University of Texas at Arlington, Arlington, Texas
- Run by
- The University of Texas at Arlington
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MDMA-Assisted Massed Exposure Therapy for PTSD
The goal of this clinical trial is to investigate the efficacy of 3,4-methylenedioxy-methamphetamine hydrochloride (MDMA) combined with Massed Prolonged Exposure (PE) therapy for the treatment of posttraumatic stress disorder (PTSD) in adult participants diagnosed with PTSD. This randomized, placeb…
- Stage
- Phase 2
- Ages
- 21 to 70
- Site
- Emory Brain Health Center, Atlanta, Georgia
- Run by
- Emory University
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Rapid Treatment of PTSD With Accelerated Non-Invasive Brain Stimulation
This study will test the clinical efficacy of an accelerated TMS (accel-TMS) protocol that rapidly addresses PTSD symptoms with 1 week (25 sessions over 5 days) of condensed treatment.
- Stage
- Not phased
- Ages
- 18 to 65
- Site
- Florida State University, Tallahassee, Florida
- Run by
- Florida State University
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Neuromodulation and Neurorehabilitation for mTBI
This study will determine (i) the magnitude of immediate and sustained effects of a current clinical standard interactive computer attention processing training (APT) when combined with intermittent theta burst stimulation (iTBS), a type of repetitive transcranial magnetic stimulation and (ii) dete…
- Stage
- Not phased
- Ages
- 18 to 80
- Site
- Northwestern University, Chicago, Illinois
- Locations
- 2 in total
- Run by
- Northwestern University
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The Impact of AMPA Receptor Blockade on Ketamine's Anti-Suicidal Effects
The purpose of this study is to test the hypothesis that the anti-depressant and anti-suicidal effects of the N-methyl-D-aspartate receptor (NMDAR) antagonist Ketamine is critically dependent on stimulation of Alpha-Amino-3-Hydroxy-5-Methyl-4-Isoxazole Propionic Acid receptors (AMPAR).
- Stage
- Phase 2
- Ages
- 21 to 65
- Site
- VA Connecticut Healthcare System, West Haven, Connecticut
- Run by
- Yale University
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Alpha-Amino-3-Hydroxy-5-Methyl-4- Isoxazole Propionic Acid Receptor Components of the Anti-Depressant Ketamine Response
The proposed study will assess the combined effect of perampanel and ketamine on the anti-depressant response in individuals with treatment resistant depression. The purpose of this study is to test the hypothesis that stimulation of Alpha-Amino-3-Hydroxy-5-Methyl-4- Isoxazole Propionic Acid recept…
- Stage
- Phase 1
- Ages
- 18 to 60
- Site
- Yale University, New Haven, Connecticut
- Run by
- Yale University
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Being Safe, Healthy, And Positively Empowered (BSHAPE) Intervention Study
The purpose of the study is to evaluate a trauma informed digital multicomponent intervention design to improve health and safety outcomes for women with lifetime exposures to violence and co-occurring PTSD and/or depression symptoms
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Johns Hopkins University, Baltimore, Maryland
- Run by
- Johns Hopkins University
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Fear and Avoidance in PTSD Patients
The purpose of this research study is to study how the brain learns to avoid certain stimuli or situations using an experimental paradigm. The big goal is to measure brain responses and subject's feelings and expectations when they are learning to actively avoid experimental stimuli, and how fear e…
- Stage
- Not phased
- Ages
- 18 to 70
- Site
- UTHealth Houston, Houston, Texas
- Run by
- The University of Texas Health Science Center, Houston
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Pimavanserin for Insomnia in Veterans With PTSD
This is a preliminary randomized, double-blind, placebo-controlled trial comparing pimavanserin 34mg at bedtime vs. placebo for the treatment of insomnia associated with post-traumatic stress disorder.
- Stage
- Phase 2
- Ages
- 18 to 64
- Site
- Michael E. DeBakey VA Medical Center, Houston, TX, Houston, Texas
- Run by
- VA Office of Research and Development
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Recovering Sleep After Trauma
The main objective of this pilot trial is to assess the feasibility and preliminary efficacy of telehealth-delivered behavioral therapy to reduce the development of posttraumatic stress and depressive symptoms following motor vehicle collision among individuals at high risk. This pilot trial will p…
- Stage
- Not phased
- Ages
- 18 to 65
- Site
- University of North Carolina at Chapel Hill, Chapel Hill, North Carolina
- Run by
- University of North Carolina, Chapel Hill
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Psychotherapy Effects on Reward Processing in PTSD
The purpose of this study is to identify how trauma-focused psychotherapy changes the function of brain circuitry in posttraumatic stress disorder (PTSD) and how this mediates improvements in the diminished ability to experience positive emotions following a traumatic or extremely stressful life ev…
- Stage
- Not phased
- Ages
- 18 to 65
- Site
- Health Discovery Building (HDB), 1601 Trinity St., Bldg B., Z0600, Austin, Texas
- Run by
- University of Texas at Austin
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Imaging Cannabinoid Receptors Using Positron Emission Tomography (PET) Scanning
The aim of the present study is to assess the availability of cannabinoid receptors (CB1R) in the human brain. CB1R are present in everyone's brain, regardless of whether or not someone has used cannabis. The investigators will image brain cannabinoid receptors using Positron Emission Tomography (P…
- Stage
- Not phased
- Ages
- 18 to 55
- Site
- Connecticut Mental Health Center, Clinical Neuroscience Research Unit, New Haven, Connecticut
- Run by
- Yale University
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Non-invasive Vagus Nerve Stimulation (nVNS) for Post-Traumatic Stress Disorder (PTSD)
The goal of this clinical trial is to evaluate the safety and effectiveness of the gammaCore non-invasive vagus nerve stimulation (nVNS) device as an additional treatment for symptoms of post-traumatic stress disorder (PTSD) in adults. The vagus nerve connects the brain with many organs and systems…
- Stage
- Not phased
- Ages
- 18 to 70
- Site
- Acacia Research Center, Sunnyvale, California
- Run by
- Acacia Clinics
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Randomized Trial of Tele Vs. Clinic TF-CBT in Puerto Rico
The current study will evaluate TF-CBT delivered via tele-health for youth presenting with trauma symptoms via a randomized controlled trial. Goals of the current study are to examine the effectiveness of Tele-TF-CBT delivered by community providers in Puerto Rico in improving youth trauma outcomes…
- Stage
- Not phased
- Ages
- 7 to 18
- Site
- Medical University of South Carolina, Charleston, South Carolina
- Run by
- Medical University of South Carolina
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Approach-Avoidance and Alcohol Challenge Study in PTSD
Individuals with posttraumatic stress disorder (PTSD) have greater prevalence of alcohol use disorders (AUDs), with this comorbidity associated with worse illness outcomes, yet there remains limited mechanistic understanding of how PTSD confers risk for AUD. Understanding risk factors that associat…
- Stage
- Not phased
- Ages
- 21 to 60
- Site
- University of Texas at Austin, Austin, Texas
- Run by
- University of Texas at Austin
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BXCL501 After Stress to Increase Recovery Success
This study will examine the safety and efficacy of BXCL501 to reduce ASR symptoms and behavioral changes among patients presenting to the Emergency Department (ED) after Motor Vehicle Collision (MVC). Specifically, the investigators will perform the BXCL501 (BASIS) Trial, a double-blind placebo-con…
- Stage
- Phase 2
- Ages
- 18 to 65
- Site
- University of Florida College of Medicine - Jacksonville, Jacksonville, Florida
- Locations
- 3 in total
- Run by
- University of North Carolina, Chapel Hill
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Nitric Oxide (NO) and Endothelial Dysfunction in Women With PTSD
This research study is conducted to better understand why women with post-traumatic stress disorder (PTSD) have higher risk of cardiovascular disease as they get older. This study looks at how trauma and PTSD affect blood vessels in young women by testing whether the dietary supplement beetroot jui…
- Stage
- Not phased
- Ages
- 18 to 40
- Site
- University of Minnesota, Minneapolis, Minnesota
- Run by
- University of Minnesota
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Personalized Brain Stimulation to Treat Chronic Concussive Symptoms
The goal of this study is to investigate a new treatment for chronic symptoms after concussion or mild traumatic brain injury in people aged 18-65 years old. Chronic symptoms could include dizziness, headache, fatigue, brain fog, memory difficulty, sleep disruption, irritability, or anxiety that oc…
- Stage
- Phase 2
- Ages
- 18 to 65
- Site
- UCLA, Westwood, Los Angeles, California
- Run by
- University of California, Los Angeles
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Induction of Dreaming With EEG and Anesthesia for Post-traumatic Stress Disorder
The goal of this study is to test whether anesthesia-induced dreaming can help alleviate symptoms of PTSD in an (1) open-label trial (Phase I) and (2) double-blind, randomized controlled trial (Phase II) in a non-surgical setting. The investigators predict that inducing and sustaining a dream state…
- Stage
- Phase 2
- Ages
- 18 to 70
- Site
- Stanford University, Stanford, California
- Run by
- Stanford University
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Cannabidiol as a Treatment for PTSD and PTSD Comorbid With TBI
This will be a randomized placebo controlled study to test the efficacy of cannabidiol (CBD) as a treatment for symptoms of post-traumatic stress disorder (PTSD). Subjects, 120 in total, will be males and females with PTSD, half of which will have comorbid mild traumatic brain injury (TBI). There w…
- Stage
- Phase 2
- Ages
- 18 to 70
- Site
- New York University School of Medicine, New York, New York
- Run by
- NYU Langone Health
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Retinal Imaging in Neurodegenerative Disease
This study aims to develop and evaluate biomarkers using non-invasive optical coherence tomography (OCT) and OCT angiography (OCTA) as well as ultra-widefield (UWF) fundus photography to assess the structure and function of the retinal and choroidal microvasculature and structure in persons with mi…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Duke University Medical Center, Durham, North Carolina
- Run by
- Duke University
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Advanced Wireless Augmented Reality-Enhanced Exposure Therapy for Posttraumatic Stress Disorder
The goal of this trial is to test how augmented reality exposure therapy (ARET) may potentiate the effects of traditional exposure therapy administered to U.S. military personnel diagnosed with PTSD. 40 adult males and females over the age of 18 that have served, or are currently serving, in the U.…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Ralph H. Johnson VA Health Care System, Charleston, South Carolina
- Run by
- Wayne State University
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Sympathetic Overactivity in Post-traumatic Stress Disorder
Post-traumatic stress disorder (PTSD) is a highly prevalent anxiety disorder that is associated with an increased risk of cardiovascular (CV) disease and hypertension. One potential mechanism is overactivation of the sympathetic nervous system (SNS), both at rest and particularly during stress. Thi…
- Stage
- Not phased
- Ages
- 18 to 65
- Site
- Atlanta VA Medical Center, Decatur, Georgia
- Run by
- Emory University
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rTMS-augmented Written Exposure Therapy for PTSD
Post-traumatic stress disorder (PTSD) is prevalent and represents a high healthcare burden among Veterans. Repetitive transcranial magnetic stimulation (rTMS) is a brain-based therapy that may be effective for treating PTSD. The theorized mechanism of rTMS is enhancement of emotional flexibility vi…
- Stage
- Not phased
- Ages
- 18 to 60
- Site
- Central Texas Veterans Health Care System, Temple, TX, Temple, Texas
- Run by
- VA Office of Research and Development
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Multifaceted Intervention to Restore Resilience and Overcome Risk
The MIRROR study will compare the effectiveness of two interventions in improving emotion regulation and reducing PTSD symptoms in female Veterans with military sexual trauma (MST) and/or intimate partner violence (IPV) and co-occurring brain injury.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Baylor College of Medicine, Houston, Texas
- Run by
- Icahn School of Medicine at Mount Sinai
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.