PTSD Clinical Trials
76 studies are recruiting for ptsd 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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Neuromodulation of the Fear Extinction Circuit Using Temporally and Anatomically Specific TMS in Humans
This study aims to explore the mechanisms of how transcranial magnetic stimulation (TMS) impacts fear circuits. The overarching objectives are to understand how varying TMS parameters affect targeted brain regions in order to optimize its impact on enhancing fear extinction memory consolidation in …
- 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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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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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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Using Exercise to Enhance Fear Extinction Learning
The goal of the current project is to establish the efficacy and mechanisms of exercise-enhanced fear extinction retrieval and generalization in posttraumatic stress disorder (PTSD). Exposure therapy is the gold standard treatment for PTSD, yet is only associated with remission rates of ~55% and in…
- Stage
- Not phased
- Ages
- 18 to 55
- Site
- Health Discovery Building, Austin, Texas
- Run by
- Josh Cisler
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Positive Processes and Transition to Health - Single-Session (PATH-SS)
The goal of this clinical trial is to test a brief, new psychotherapy (called Positive Processes and Transition to Health - Single Session, or PATH-SS) that aims to provide relief for people who are suffering after experiencing a sexual assault. This research will explore whether this new psychothe…
- Stage
- Not phased
- Ages
- 18 to 65
- Site
- Case Western Reserve University, Cleveland, Ohio
- Run by
- Case Western Reserve University
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A Trial Comparing Interpersonal Therapy to Exposure Therapy for PTSD Due to Military Sexual Trauma (MST) in Male and Female Military Personnel
The purpose of this study is to compare two kinds of therapy for Posttraumatic Stress Disorder (PTSD): exposure therapy (ET) and Interpersonal Psychotherapy (IPT). The results of this study will allow us to see if IPT and ET are equally effective in treating PTSD due to Military Sexual Trauma, with…
- Stage
- Not phased
- Ages
- 18 to 85
- Site
- Weill Cornell Medicine, New York, New York
- Run by
- Weill Medical College of Cornell University
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Microbiome Modulation With Prebiotics in PTSD and Cirrhosis
Despite medical advancements, PTSD remains a major issue in Veterans1. Current treatment strategies have relatively poor adherence. In patients with PTSD and cirrhosis, there is greater cognitive impairment as well as changes in gut microbiome structure and function2,3. In addition, when there is c…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Hunter Holmes McGuire VA Medical Center, Richmond, Virginia
- Run by
- Hunter Holmes Mcguire Veteran Affairs Medical Center
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Multiphase Optimization Strategy (MOST) for Treating Pediatric Post-traumatic Stress Disorder (PTSD)
The goal of this clinical trial is to test the extent to which different treatment components work to improve pediatric post-traumatic stress disorder (PTSD). It will also provide evidence for how these components work. The main research questions are: What are the effects of different components u…
- Stage
- Not phased
- Ages
- 8 to 17
- Site
- The Mt. Hope Family Center, Rochester, New York
- Run by
- University of Rochester
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Cognitive Processing Therapy (CPT) Memory Support (MS) Study
The efficacy of psychological interventions for posttraumatic stress disorder (PTSD) is likely limited by the difficulty participants have learning and remembering important therapy content. Accordingly, the present study will examine the utility of integrating a Memory Support (MS) intervention in…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- VA Boston Healthcare System, Jamaica Plain, Massachusetts
- Run by
- Boston University
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Repurposing Low-Dose Clonidine for PTSD in Veterans
Hypothesis: Veterans with PTSD prescribed clonidine will demonstrate improvements in PTSD symptoms, including daytime, nighttime, and sleep-related behaviors.
- Stage
- Phase 3
- Ages
- 18 and older
- Site
- Aurora Psychiatric Hospital, Wauwatosa, Wisconsin
- Run by
- Wake Forest University Health Sciences
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Psychological Trauma, Post-Traumatic Stress Disorder, and Resilience in Adults With Congenital Heart Disease
The purpose of this study, entitled "Psychological trauma, post-traumatic stress disorder, and resilience in adults with congenital heart disease in a large population sample", is to evaluate for exposures during a lifetime with congenital heart disease that may be associated with higher likelihood…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire
- Locations
- 3 in total
- Run by
- Dartmouth-Hitchcock Medical Center
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Integrative Bilateral Cervical Sympathetic Blocks for Trauma-Related Symptoms in Special Operations Veterans: A Prospective Case Series
This study prospectively evaluates the effects of Integrative Bilateral Cervical Sympathetic Block (BCSB) on trauma-related symptoms in Special Operations Veterans, comparing outcomes in those receiving BCSB alone versus BCSB combined with structured integrative therapy. Using standardized FDA-appr…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Reset Medical and Wellness Center, Strongsville, Ohio
- Run by
- Reset Medical and Wellness Center
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Testing an Integrated PTSD and Weight Management Intervention: A Hybrid Type 1 Trial
Obesity and post-traumatic stress disorder (PTSD) are common among Veterans. PTSD increases risk for obesity, impacting functioning, health, quality of life, and premature mortality. Use of proven treatments for PTSD and obesity in VA is low. Furthermore, Veterans with PTSD lose less weight than th…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- VA Puget Sound Health Care System Seattle Division, Seattle, WA, Seattle, Washington
- Run by
- VA Office of Research and Development
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The ED-AWARENESS-2 Trial
The investigators will screen all mechanically ventilated ED patients for study eligibility and will enroll all consecutive patients satisfying inclusion and exclusion criteria. The study design is a pragmatic, multicenter, stepped wedge cluster randomized trial, enrolling at five sites over a 3-ye…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Roy J. and Lucille A. Carver College of Medicine, Iowa City, Iowa
- Locations
- 4 in total
- Run by
- Washington University School of Medicine
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Behavioral Health Collaborative Care Model in an ICU Recovery Clinic
Survivors of critical illness are at high risk for mental health issues such as anxiety, depression, and PTSD. This single-site, randomized controlled trial at the Medical University of South Carolina will enroll 150 patients to compare outcomes between a behavioral health Collaborative Care Model …
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Medical University of South Carolina, Charleston, South Carolina
- Run by
- Medical University of South Carolina
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Behavioral Health Collaborative Care Model in Post-ICU Clinic Family Pilot
This pilot study evaluates the feasibility and acceptability of implementing a Behavioral Health Collaborative Care Model (BH CoCM) for family members of ICU survivors. The intervention includes telehealth-enabled behavioral health assessments and access to the NeuroFlow platform. A subset of parti…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Medical University of South Carolina, Charleston, South Carolina
- Run by
- Medical University of South Carolina
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Open-Label Psilocybin Study in Transdiagnostic Population
The primary objective of this study is to investigate the safety, feasibility, and tolerability of psilocybin treatment in individuals with functional impairment due to psychiatric symptoms. The secondary objective of this study is to determine whether individuals with functional impairments due to…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Connecticut Mental Health Center - Yale School of Medicine, New Haven, Connecticut
- Run by
- Yale University
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A Mixed Methods Pilot Trial of the STEP Home Workshop to Improve Reintegration and Reduce Suicide Risk for Recently Transitioned Veterans
Risk of Veteran suicide is elevated during the first year of transition from military service to civilian life. Most Veteran suicides occur among Veterans who are not connected to VA healthcare. Suicide prevention and connection to care are therefore critical for recently transitioning Veterans. Tr…
- Stage
- Not phased
- Ages
- 18 to 65
- Site
- VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA, Boston, Massachusetts
- Run by
- VA Office of Research and Development
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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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The BEAR Program for Women With Trauma Who Have Suicidal Thoughts
The current study aims to test the feasibility of a new form of group therapy for women who have a history of interpersonal trauma and current suicidal ideation. The Building Empowerment and Resilience (BEAR) Therapeutic group has been adapted for women who have experienced trauma and have current …
- Stage
- Not phased
- Ages
- 18 to 75
- Site
- Stanford University School of Medicine, Stanford, California
- Run by
- Stanford University
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Trauma BPE Prolonged Exposure Therapy for Injured Individuals Admitted to a Level I Trauma Center
The purpose of this research is to determine if a brief treatment method is effective for preventing posttraumatic stress disorder (PTSD) and a number of other concerns following injury.
- Stage
- Not phased
- Ages
- 18 to 75
- Site
- Baylor University Medical Center, Dallas, Texas
- Locations
- 3 in total
- Run by
- Baylor Research Institute
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Enhancing Rehabilitation for Veterans With Serious Mental Illness
This study addresses the critical need for innovative therapeutic interventions in Veterans with serious mental illnesses (SMI) receiving care in VA Psychosocial Rehabilitation and Recovery Centers (PRRCs). The vast majority of individuals with SMI suffer from cognitive impairments, leading to chro…
- Stage
- Not phased
- Ages
- 18 to 83
- Site
- VA San Diego Healthcare System, San Diego, CA, San Diego, California
- Run by
- VA Office of Research and Development
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PTSD Treatment for Incarcerated Men and Women: AV
This research will help identify if a PTSD treatment group, called Cognitive Processing Therapy (CPT), that is used in community settings is helpful in reducing PTSD symptoms among people who are incarcerated. The goal of CPT is to create a space for people to modify unhelpful beliefs related to tr…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Psychiatric Institute and Clinic, Madison, Wisconsin
- Run by
- University of Wisconsin, Madison
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Phase IIa Trial of a Selective Glucocorticoid Receptor Antagonist in the Treatment of Veterans With Posttraumatic Stress Disorder (PTSD) (Seven Study)
The purpose of this study is to test the drug CORT108297, which blocks the hormone cortisol, for treatment of PTSD in Veterans, and establish a safety profile that will inform the design of future studies.
- Stage
- Phase 2
- Ages
- 18 to 69
- Site
- Tuscaloosa VA Medical Center, Tuscaloosa, AL, Tuscaloosa, Alabama
- Locations
- 2 in total
- Run by
- VA Office of Research and Development
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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
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.