Stress Disorders, Post-Traumatic Clinical Trials
18 studies are recruiting for stress disorders, post-traumatic 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 now recruiting
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MOCHA: Embedded Inpatient Mental Health Care for High-Risk Perinatal Patients
Pregnant and postpartum patients hospitalized for medical complications experience high rates of depression, anxiety, and trauma-related symptoms, yet access to timely psychiatric care during obstetric hospitalization is limited. Project MOCHA integrates early mental health screening, trauma-inform…
- Stage
- Not phased
- Ages
- 18 to 100
- Site
- Riley Hospital for Children at Indiana University Health, Indianapolis, Indiana
- Run by
- Indiana University
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Massed Prolonged Exposure for PTSD in Substance Use Treatment
The goal of this clinical trial is to learn if receiving Prolonged Exposure Therapy for PTSD in massed format (multiple sessions weekly) is as effective as receiving it with sessions once per week among veterans with PTSD and substance use disorder in intensive outpatient substance use treatment. T…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- VA San Diego Healthcare System, San Diego, California
- Locations
- 6 in total
- Run by
- Veterans Medical Research Foundation
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Trauma-Informed Guilt Reduction Therapy Compared to Prolonged Exposure
The goal of this clinical trial is to learn if receiving Trauma-Informed Guilt Reduction (TrIGR) Therapy is as effective as receiving Prolonged Exposure Therapy among veterans with PTSD and trauma related guilt. The main questions it aims to answer are: Will TrIGR be comparable to PE in terms of PT…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Little Rock Veterans Health Care System (LRVHCS), Little Rock, Arkansas
- Locations
- 4 in total
- Run by
- Veterans Medical Research Foundation
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SMART Therapist Training: A Hybrid Factorial-SMART Design
Cognitive Processing Therapy (CPT) is highly effective in randomized controlled trials, but its effectiveness drops substantially in standard clinical practice, largely due to therapist "drift" from fidelity to the protocol. What remains unknown is which components of CPT training yield high therap…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- VA Palo Alto Health Care System, Palo Alto, CA, Palo Alto, California
- Locations
- 4 in total
- Run by
- VA Office of Research and Development
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Enhancing Memory in Cognitive Processing Therapy for PTSD
Several psychotherapies for posttraumatic stress disorder (PTSD) have a strong evidence base for their efficacy, but nonresponse rates are high, particularly among older Veterans. Accumulating evidence indicates that memory deficits and poor learning of therapy contents adversely affect psychothera…
- Stage
- Not phased
- Ages
- 60 and older
- Site
- Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA, Philadelphia, Pennsylvania
- Run by
- VA Office of Research and Development
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Computational Assessment of GABA Receptor Modulation in PTSD
A substantial majority of Veterans with posttraumatic stress disorder (PTSD) continue to suffer even with the best current medications. Progress in developing more effective medications is hampered by the substantial variability within Veterans with PTSD, meaning the most effective medication likel…
- Stage
- Phase 4
- Ages
- 18 to 65
- Site
- VA San Diego Healthcare System, San Diego, CA, San Diego, California
- Run by
- VA Office of Research and Development
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Manage Emotions to Reduce Aggression (MERA)
PTSD is one of the most prevalent mental health conditions affecting Veterans who have served since 9/11. Veterans with posttraumatic stress disorder (PTSD) report difficulty controlling impulsive aggression (IA). An inability to manage one's emotions (emotion dysregulation) is an underlying mechan…
- Stage
- Not phased
- Ages
- 18 to 64
- Site
- James A. Haley Veterans' Hospital, Tampa, FL, Tampa, Florida
- Locations
- 2 in total
- Run by
- VA Office of Research and Development
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Role of Sympathetic Overactivity and Angiotensin II in PTSD and CV
The purpose of this study is to find out why patients with post-traumatic stress disorder (PTSD) have an increased risk for heart disease and high blood pressure later in life. A second purpose is to find out what causes PTSD patients to have high adrenaline levels during stress. This study will al…
- Stage
- Phase 2
- Ages
- 18 to 65
- Site
- Atlanta VA Medical Center, Decatur, Georgia
- Run by
- Emory University
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Mismatch vs. Standard Intervention During Memory Reconsolidation Blockade With Propranolol: Effect on Psychophysiological Reactivity During Traumatic Imagery
The proposed R21 project will attempt to further develop a novel intervention for posttraumatic stress symptoms inspired by the science of memory reconsolidation. Work in normal humans has shown that when a stable, consolidated memory is reactivated (i.e., retrieved) under appropriate conditions, i…
- Stage
- Phase 4
- Ages
- 18 to 65
- Site
- Massachusetts General Hospital Home Base Program, Charlestown, Massachusetts
- Run by
- Massachusetts General Hospital
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Enhancing PTSD Treatment Outcomes by Improving Patient-Provider Communication
The purpose of this clinical trial is to learn whether existing treatments for posttraumatic stress disorder (PTSD) can be improved. Two treatments for PTSD, cognitive processing therapy (CPT) and prolonged exposure (PE) will be studied. CPT and PE are effective treatments that are widely available…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- National Center for PTSD at VA Boston Healthcare System, Boston, Massachusetts
- Run by
- Boston University
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A Study of a Novel EEG Neurofeedback System for PTSD Treatment
The goal of this clinical trial is to learn if training with the Prism system can reduce PTSD symptoms in US military Veterans and civilians with PTSD. Prism is a form of neurofeedback training that uses EEG signals to promote self-regulation of brain function. The main question this study aims to …
- Stage
- Not phased
- Ages
- 18 to 65
- Site
- Birmingham VA Medical Center, Birmingham, Alabama
- Locations
- 6 in total
- Run by
- Foundation for Atlanta Veterans Education and Research, Inc.
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MDMA for Co-occurring PTSD and OUD After Childbirth
This is an open-label study of the use of MDMA Assisted Therapy for postpartum people with co-occurring Post Traumatic Stress Disorder (PTSD) and Opioid Use Disorder (OUD). The study protocol has been adapted from the Phase 3 studies sponsored by the Multidisciplinary Association for Psychedelic St…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- University of New Mexico Health Sciences, Albuquerque, New Mexico
- Run by
- University of New Mexico
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Transcutaneous Vagal Nerve Stimulation in Veterans With Posttraumatic Stress Disorder
This study effects the effects of transcutaneous cervical vagal nerve stimulation (tcVNS) or a sham control on brain, physiology, and PTSD symptoms in Veterans with posttraumatic stress disorder (PTSD). Veterans undergo brain imaging and physiological measures in conjunction with traumatic scripts …
- Stage
- Not phased
- Ages
- 18 to 75
- Site
- Atlanta VA Medical and Rehab Center, Decatur, GA, Decatur, Georgia
- Run by
- VA Office of Research and Development
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Healthy Recovery After Trauma Study
Mental contamination-an internal experience of dirtiness evoked in the absence of physical contact with an external source-has been linked to the development and maintenance of posttraumatic stress disorder (PTSD) following exposure to sexual abuse or assault (Adams et al., 2014; Badour et al., 201…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Kentucky Clinic for Emotional Health (CEH), Lexington, Kentucky
- Run by
- Christal L Badour
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Postpartum Care in the NICU (PeliCaN) Transitions
This is a randomized controlled trial of a dyad-centered, doula support and healthcare coordination model of care in a large urban neonatal intensive care unit (NICU), which serves a high-risk, low-income, majority Black population. In addition to doula support and coordination of care in the NICU,…
- Stage
- Not phased
- Ages
- 16 and older
- Site
- Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania
- Run by
- University of Pennsylvania
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Combining Stellate Ganglion Block With Prolonged Exposure for PTSD
The goal of this clinical trial is to compare the combination of Massed Prolonged Exposure (PE); a behavioral therapy for PTSD) and a stellate ganglion block (SGB; an injection of a local anesthetic into the front of the neck) with Massed Prolonged Exposure and a sham injection in a sample of milit…
- Stage
- Phase 2
- Ages
- 18 to 65
- Site
- Carl R. Darnall Army Medical Center, Fort Hood, Texas
- Locations
- 2 in total
- Run by
- The University of Texas Health Science Center at San Antonio
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Computer Monitor vs Augmented Reality 3MDR for PTSD PTSD: A Randomized Controlled Trial
This is a prospective randomized controlled trial comparing two ways of delivering Motion-assisted, Multi-modular Memory Desensitization and Reconsolidation (3MDR) therapy for posttraumatic stress disorder (PTSD). The study seeks 60 volunteers who have PTSD and are eligible for care in the Departme…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Uniformed Services University, Bethesda, Maryland
- Run by
- Uniformed Services University of the Health Sciences
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An Evaluation of Two PTSD Assessments in an Active Duty and Military Veteran Sample
Given the high prevalence of post-traumatic stress disorder (PTSD) in veterans and active duty military, the focus of this research study is to test the reliability of two new PTSD assessments, the Clinician Administered PTSD Scale for DSM-5 (CAPS-5) and the PTSD Symptom Scale Interview for DSM-5 (…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Tripler Army Medical Center, Honolulu, Hawaii
- Locations
- 3 in total
- Run by
- U.S. Army Medical Research and Development Command
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.