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AzTrials

Condition

PTSD Clinical Trials

Studies of ptsd, matched by condition name and medical subject headings. Start with those open to enrolment.

2,689 registered studies

In numbers

Open to volunteers
549
Active
632
With results posted
509
All registered
2,689

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 549
  • Stress Disorders, Post-Traumatic

    Salience Network Informed rTMS for PTSD

    • Not yet recruiting
    • Age: 18 to 60 years
    • Medical device

    The proposed study will test whether magnetic resonance imaging (MRI)-guided transcranial magnetic stimulation (TMS) can reduce posttraumatic stress disorder (PTSD) symptoms in Veterans.

    Trial name
    NCT07886840
    Testing
    Active MRI-Guided intermittent theta burst stimulation (iTBS)
    Where
    United States
    Volunteers
    84 people
    Sponsor
    VA Office of Research and Development
    Can I take part? NCT07886840
  • Pregnancy Early, PTSD

    PTSD Screening in Pregnant Black Women

    • Recruiting
    • Age: 18 years and older
    • Lifestyle or therapy programme

    This study will compare the effectiveness of two active screening interventions in improving post-traumatic stress disorder (PTSD) symptoms, maternal perinatal care utilization, satisfaction utilization of mental healthcare…

    Trial name
    NCT06522022
    Testing
    Culturally Responsive SBIRT for OB, Brief Screening for PTSD
    Where
    2 sites in United States
    Volunteers
    804 people, healthy volunteers welcome
    Sponsor
    Emory University
    Can I take part? NCT06522022
  • Post-Traumatic Stress Disorder

    Randomized Trial of Tele Vs. Clinic TF-CBT in Puerto Rico

    • Recruiting
    • Age: 7 to 18 years
    • Lifestyle or therapy programme

    The current study will evaluate TF-CBT delivered via tele-health for youth presenting with trauma symptoms via a randomized controlled trial.

    Trial name
    NCT06332209
    Testing
    Trauma Focused Cognitive Behavioral Therapy
    Where
    United States
    Volunteers
    80 people
    Sponsor
    Medical University of South Carolina
    Can I take part? NCT06332209
  • Traumatic Brain Injuries, TBI (Traumatic Brain Injury)

    Rehabilitation Through Virtual Immersion & Integrated Exposure for Mild Traumatic Brain Injury (ReVIVE for mTBI)

    • Recruiting
    • Age: 18 to 55 years
    • Phase 1
    • Medical device
    • Lifestyle or therapy programme

    The primary goal of this study is to evaluate the effectiveness of an integrated therapeutic model - combining VR and standard psychotherapy in improving executive function and hyperarousal adults impacted with mTBI.

    Conditions
    Traumatic Brain Injuries, TBI (Traumatic Brain Injury), MTBI - Mild Traumatic Brain Injury, mTBI
    Trial name
    ReVIVE (NCT07890337)
    Testing
    Virtual Reality, Standard Psychotherapy
    Where
    United States
    Volunteers
    30 people
    Sponsor
    Johns Hopkins University
    Can I take part? ReVIVE
  • PTSD - Post Traumatic Stress Disorder, PTSD

    Redefine Study: A Study Evaluating the Efficacy, Safety, and Tolerability of COMP360 in Participants With Post-traumatic Stress Disorder

    • Recruiting
    • Age: 18 years and older
    • Phase 2/3

    The Redefine Study (COMP202) is testing COMP360 to see if it may reduce post-traumatic stress disorder (PTSD) symptoms when administered alongside monitoring and support from a trained study team.

    Conditions
    PTSD - Post Traumatic Stress Disorder, PTSD, PTSD Symptoms, PTSD, Post Traumatic Stress Disorder
    Trial name
    Redefine (NCT07570654)
    Testing
    COMP360 psilocybin
    Where
    10 sites in United States, Canada
    Volunteers
    300 people
    Sponsor
    COMPASS Pathways
    Can I take part? Redefine
  • Major Depression

    Psilocybin Intervention for Veterans Overcoming Treatment-Resistant Depression

    • Recruiting
    • Age: 18 to 75 years
    • Phase 3

    The purpose of this multi-site randomized controlled trial is to evaluate the efficacy and risks of psilocybin for the treatment of depression in U.S.

    Trial name
    PIVOT (NCT07226232)
    Testing
    Psilocybin
    Where
    5 sites in United States
    Volunteers
    240 people
    Sponsor
    VA Office of Research and Development
    Can I take part? PIVOT
  • Insomnia, Depression - Major Depressive Disorder

    Enhancing Operational Readiness With Digital Self-Managed Cognitive Behavioral Therapy for Insomnia (CBTI)

    • Not yet recruiting
    • Age: 18 to 55 years
    • Lifestyle or therapy programme

    The goal of this pilot clinical trial is to evaluate the effectiveness and delivery method of a CBTI self-managed digital mobile application in service members. The main questions it aims to answer are: RQ1.

    Conditions
    Insomnia, Depression - Major Depressive Disorder, PTSD
    Trial name
    NCT07335276
    Testing
    Cognitive Behavioral Therapy for Insomnia
    Volunteers
    144 people
    Sponsor
    Madigan Army Medical Center
    Can I take part? NCT07335276
  • Acute Stress Reaction, Acute Stress Disorder

    Prevention/Reduction of ASRs and PTSD to Sustain Civilian Performance With Sublingual Cyclobenzaprine HCl (TNX-102 SL)

    • Recruiting
    • Age: 18 to 55 years
    • Phase 2

    This study will examine the safety and efficacy of TNX-102 SL to reduce ASR symptoms and behavioral changes among patients presenting to the emergency department (ED) after motor vehicle collision (MVC).

    Conditions
    Acute Stress Reaction, Acute Stress Disorder, Neurocognitive Function, Post-traumatic Stress
    Trial name
    OASIS (NCT06636786)
    Testing
    Cyclobenzaprine HCl
    Where
    9 sites in United States
    Volunteers
    180 people
    Sponsor
    University of North Carolina, Chapel Hill
    Can I take part? OASIS
  • PTSD

    Exercise and Emotional Learning in Posttraumatic Stress Disorder

    • Recruiting
    • Age: 18 to 64 years
    • Lifestyle or therapy programme

    The goal of this clinical trial is to test how exercise affects learning and memory processes relevant to the treatment of PTSD. Participants will complete a baseline intake followed by two experimental sessions.

    Trial name
    NCT06127342
    Testing
    Moderate Intensity Exercise, Low Intensity Exercise
    Where
    2 sites in United States
    Volunteers
    100 people
    Sponsor
    Christal L Badour
    Can I take part? NCT06127342
  • PTSD, Suicidal Thoughts and Behaviors

    Cannabis, Neuroinflammation, and Suicidal Ideation: A Supplemental Brain Imaging Study

    • Enrolling by invitation
    • Age: 19 to 69 years
    • Observational study

    This study will be the first to use brain imaging to explore how cannabis affects the brain and inflammation in U.S. military veterans with PTSD.

    Conditions
    PTSD, Suicidal Thoughts and Behaviors, PTSD Symptoms, Depressive Symptoms
    Trial name
    CNS (NCT07222306)
    Testing
    1-(2-[+F]fluoroethyl)-L-tryptophan
    Where
    United States
    Volunteers
    100 people
    Sponsor
    Wayne State University
    Can I take part? CNS

Completed, with results posted

All 461
  • Stress Disorders, Post-Traumatic, Affect

    Examining Effects of a Therapeutic Focus on Positive Memories on Post-Trauma Health

    • Completed
    • Age: 18 to 65 years
    • Lifestyle or therapy programme
    • Results posted

    Posttraumatic stress disorder (PTSD) has devastating health consequences. Evidence-based PTSD interventions address the substantial burden of PTSD on the health of individuals and societies; however, several individuals receiving…

    Conditions
    Stress Disorders, Post-Traumatic, Affect, Memory
    Trial name
    NCT05523453
    Testing
    Processing of Positive Memories Technique (PPMT), Supportive Counseling (SC)
    Where
    United States
    Volunteers
    70 people
    Sponsor
    University of North Texas, Denton, TX
    Can I take part? NCT05523453
  • Post-traumatic Stress Disorder

    Ketamine and Prolonged Exposure in PTSD

    • Completed
    • Age: 18 to 75 years
    • Phase 1/2
    • Results posted

    This study aims at investigating the effectiveness of the drug, Ketamine, in combination with Prolonged Exposure (PE) therapy for people suffering from PTSD.

    Trial name
    NCT03960658
    Testing
    ketamine-enhanced prolonged exposure
    Where
    United States
    Volunteers
    12 people
    Sponsor
    Minneapolis Veterans Affairs Medical Center
    Can I take part? NCT03960658
  • Stress Disorders, Post-Traumatic

    Safety Aid Reduction Treatment for PTSD Among Veterans

    • Completed
    • Age: 18 years and older
    • Lifestyle or therapy programme
    • Results posted

    The purpose of this project is to examine the acceptability, feasibility, and utility of a safety aid reduction treatment (START) among Veterans with posttraumatic stress disorder (PTSD).

    Trial name
    START-PTSD (NCT04515784)
    Testing
    Safety Aid Reduction Treatment for PTSD
    Where
    United States
    Volunteers
    45 people
    Sponsor
    VA Office of Research and Development
    Can I take part? START-PTSD
  • Post Traumatic Stress Disorder

    Remotely Resolving Psychological Stress (Remote RePS)

    • Completed
    • Age: 18 years and older
    • Medical device
    • Results posted

    The investigators have developed a mobile app called Resolving Psychological Stress (REPS) for people with posttraumatic stress disorder (PTSD).

    Trial name
    NCT03196999
    Testing
    Personalized Attention Bias Training, Neutral Attention Training Condition, Non-Personalized Attention Bias Training
    Where
    United States
    Volunteers
    689 people
    Sponsor
    University of California, San Francisco
  • Posttraumatic Stress Disorder

    Neurosteroids for Treatment of PTSD in Veterans

    • Completed
    • Age: 18 to 65 years
    • Phase 2
    • Results posted

    This study seeks to determine if pregnenolone can improve symptoms of PTSD and other symptoms that commonly occur with PTSD in Iraq/Afghanistan-era Veterans. The total study duration for each participant is 10 weeks.

    Trial name
    NCT03799562
    Testing
    Pregnenolone
    Where
    United States
    Volunteers
    97 people
    Sponsor
    VA Office of Research and Development
    Can I take part? NCT03799562

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