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Stress Disorders, Post-Traumatic clinical trials

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NCT ID: NCT02824445 Terminated - Clinical trials for Post-Traumatic Stress Disorders

To Evaluate the Efficacy of EEG-guided Magnetic Resonant Therapy in War Veterans With Posttraumatic Stress Disorder

Start date: May 2015
Phase: N/A
Study type: Interventional

After 13 years of war, PTSD has become pervasive in service members. Traditionally it is evaluated by PTSD Checklist Military Version (PCL-M) and treated with cognitive processing therapy, prolonged exposure therapy and medication management with limited success. Repetitive Transcranial Magnetic Stimulation (TMS) has shown efficacy for improving individual cognitive function in the past decades, both in healthy population and in patients with depression. TMS has been approved by the FDA in treatment of major depressive disorder and migraine headaches. Magnetic EEG guided Resonant Treatment (MeRT) is a form of individualized TMS based on member's EEG/ECG input. Investigators propose to use MeRT to treat veterans with war-related PTSD, a syndrome that includes depressive and anxious symptoms; it is likely that MeRT (namely TMS) will be beneficial and comparable to or better than the current FDA approved methods for treating PTSD.

NCT ID: NCT02816788 Terminated - Clinical trials for Stress Disorders, Post-Traumatic

Investigation of Equine Assisted Therapy for Post-Traumatic Stress Disorder

Start date: June 20, 2017
Phase: N/A
Study type: Interventional

In partnership with SARI Therapeutic Riding (SARI TR) and other equine therapy locations, Brescia University College, at the University of Western Ontario, will study the use of Equine Assisted Therapy (EAT) for military veterans and "first reponders" (emergency services personell) diagnosed with Post-Traumatic Stress Disorder. Data will be collected through tests and questionnaires, and follow-up interviews with participants. It is expected that after a series of EAT sessions, the social, emotional and psychological well-being of participants will be improved and PTSD symptoms alleviated.

NCT ID: NCT02737488 Terminated - Trauma Clinical Trials

Helping Children With Trauma

Start date: February 1, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate if a trauma treatment called Trauma Systems Therapy (TST) decreases children's mental health symptoms (such as acting out, not controlling their emotions, etc.) as a result of a traumatic event (or events). A traumatic event or events can include experiencing or witnessing violence, excessive bullying, war, car accident, serious injury, getting mistreated or anything else that makes one feel scared or frightened. Children/teens who experience traumatic events have been shown to be at higher risk of poor mental and physical health. Trauma can impact family life, school life and interpersonal relationships well into adulthood. Unfortunately, most children who have experienced traumatic events do not undergo treatment. Although promising treatments do exist, most do not address the complexity of trauma, particularly related to ongoing stress and threats to safety in their environments. One hundred and twenty eligible youth will be randomized to receive either treatment with TST at NYU's Child Study Center or trauma treatment as usual (TAU) at a community mental health clinic. It is hypothesized that: - Youth receiving TST will demonstrate a greater decrease in Post-Traumatic Stress Disorder (PTSD) symptoms at the 3, 6, and 9-month follow-up assessments compared to youth receiving treatment as usual (TAU) in the community. - Youth receiving TST will demonstrate a greater decrease in symptoms of depression, anxiety and problem behaviors (aggression, violence, self-destructive behaviors, etc.) at the 3-, 6- and 9-month follow-up assessments compared to youth receiving TAU. - Youth receiving TST will have fewer acute mental health service events, such as psychiatric hospitalizations and ED visits compared to youth receiving TAU. - Greater fidelity to the TST model is associated with better treatment outcomes among youth receiving TST.

NCT ID: NCT02727998 Terminated - Clinical trials for Posttraumatic Stress Disorder

Intensive 7-day Treatment for PTSD Combining Ketamine With Exposure Therapy

PTSD
Start date: December 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to combine a single infusion of Ketamine with 7-days of trauma focus psychotherapy to relieve post traumatic stress disorder (PTSD) symptoms more effectively. This treatment has the potential to produce a significant therapeutic effect that otherwise would take months to occur.

NCT ID: NCT02661828 Terminated - Clinical trials for Major Depressive Disorder

Tapering Off Antidepressants

Start date: January 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to compare two ways to stop taking an antidepressant medication and determine whether a faster or slower taper is better tolerated.

NCT ID: NCT02610049 Terminated - Clinical trials for Post-traumatic Stress Disorder

Trial of Art Therapy During Cognitive Processing Therapy for PTSD

Art_Tx_PTSD
Start date: November 2013
Phase: N/A
Study type: Interventional

This is a randomized, controlled trial of adjunctive art therapy during cognitive processing therapy for PTSD.

NCT ID: NCT02520726 Terminated - Clinical trials for Post-traumatic Stress Disorder

PTSD Prevention Study Examining the Efficacy of Sertraline in Burn Victims

Start date: September 2013
Phase: Phase 4
Study type: Interventional

This is a randomized, double-blind, placebo-controlled study to determine whether administration of sertraline to patients who exhibit acute stress disorder secondary to severe burns can contribute to the prevention of post-traumatic stress disorder (PTSD).

NCT ID: NCT02479906 Terminated - Clinical trials for Post-Traumatic Stress Disorder

A Safety & Efficacy Study With Deep Transcranial Magnetic Stimulation for the Treatment of Post-Traumatic Stress Disorder (PTSD)

Start date: November 17, 2016
Phase: N/A
Study type: Interventional

The purpose of the present study is to evaluate the safety and efficacy of Brainsway Deep TMS (DTMS) for the treatment of PTSD.

NCT ID: NCT02369614 Terminated - Clinical trials for PTSD - Post Traumatic Stress Disorder

Low -vs- High-Frequency Repetitive TMS of the Right Dorsolateral Prefrontal Cortex in PTSD

Start date: August 2014
Phase: N/A
Study type: Interventional

This is a randomized placebo/sham controlled, double-blind study investigating the efficacy of high- and low-frequency rTMS applied to the right DLPFC at either 1 Hz, 10 Hz, or sham rTMS as compared to an OASIS treatment as usual group for the treatment of PTSD symptoms.

NCT ID: NCT02334566 Terminated - Clinical trials for Post-Traumatic Stress Disorder

Lending a Hand to Our Future: PTSD in Refugee Children and Youth

LHOF
Start date: August 2015
Phase: N/A
Study type: Interventional

Immigrant and refugee children and youth are the fastest growing segment of Canadian society, but their mental health is too often overlooked even though their high rates of symptoms are increasingly of concern. These children and youth face the same developmental challenges as other children, but migration and resettlement amplify challenges and also create additional risks. Although a literature about the effects of immigrant family life on the mental health of children exists, very little research has examined the specific extent and implications of post-traumatic stress disorder (PTSD) among refugee children and youth. In addition, the best practice intervention strategies that most optimally support their mental health difficulties have not been evaluated. This study investigates the effectiveness of a treatment intervention in a sample of refugee children: Narrative Exposure Therapy or NET and KIDNET (developed for younger children), selected due to their documented superiority relative to other forms of treatment for children and youth with PTSD.