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Posttraumatic Stress Disorders clinical trials

View clinical trials related to Posttraumatic Stress Disorders.

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NCT ID: NCT04504903 Active, not recruiting - Clinical trials for Posttraumatic Stress Disorders

Cognitive Behavioral Therapy to Improve Work and Wellness in Veterans With Mental Illness

WORKWELL
Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Vocational instability in Veterans with serious mental illness (SMI) is pervasive, costly, and harmful. Over 75% of Veterans with SMI are unemployed, resulting in economic difficulties and trouble meeting basic needs. Overall, among adults with depression, work dysfunction results in a 36 to 51 billion dollar loss annually. Unemployed Veterans with SMI also suffer major health consequences, including a more severe course of illness and poor recovery over time, leading to increased inpatient and emergency service use. The WORKWELL study will synergistically address these deficits in health, recovery, and work functioning by testing the Cognitive Behavioral Therapy for Work Success (CBTw) intervention. Using a pragmatic design, this project will address work as a major social determinant of health and close the health disparity gap among people with SMI. Further, through promotion of work and healthy thinking, CBTw holds promise to reduce risk of suicide among vulnerable veterans with SMI.

NCT ID: NCT01157416 Active, not recruiting - PTSD Clinical Trials

Effect of D-cycloserine on Treatment of Posttraumatic Stress Disorder (PTSD) in Youth

Start date: June 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to show whether D-cycloserine in combination with cognitive behavioral therapy (CBT) is more effective than CBT alone to reduce symptoms of posttraumatic stress disorder (PTSD) in 7-12 year old children.

NCT ID: NCT00965809 Active, not recruiting - Clinical trials for Posttraumatic Stress Disorders

Add on Study on Δ9-THC Treatment for Posttraumatic Stress Disorders (PTSD)

THC_PTSD
Start date: October 2009
Phase: Phase 4
Study type: Interventional

Stress Disorder (PTSD) is a chronic and debilitating anxiety disorder which is widespread in every social level and is very prevalent in outpatient and inpatient settings. A recent open-label study showed that the synthetic cannabinoid receptor agonist Nabilone had beneficial effects abolishing or greatly reducing nightmares that persisted in spite of treatment with conventional PTSD medications. Furthermore, a big number of patients suffering from chronic PTSD report using smoked marijuana because its tranquilizing effect and sleep quality improvement. According to clinical and epidemiological data different derivates from the cannabis plant are illegally and pervasively consumed by PTSD patients in order to reduce distress. The aim of the proposed study is to broaden the previous observations and to measure the extent to which Δ 9-THC will bring to significant improvement on the full spectrum of PTSD symptoms.

NCT ID: NCT00958217 Active, not recruiting - Depressive Symptoms Clinical Trials

Intervention for Veterans With Depression, Substance Disorder, and Trauma

Start date: December 2009
Phase: Phase 0
Study type: Interventional

This study will compare two different types of psychotherapy for Veterans with depression, addiction, and a past traumatic experience. Everyone in the study will receive 12 weeks of group cognitive behavioral therapy focused on depression and addiction, followed by 12 weeks of individual psychotherapy sessions. For the second 12 weeks, half of the people will receive a review of the initial therapy, and half will receive a cognitive behavioral therapy focused on trauma. Everyone will complete research interviews every 3 months for a total of 18 months.

NCT ID: NCT00831727 Active, not recruiting - Clinical trials for Posttraumatic Stress Disorders

The Role of Affect Regulation and Self-presentation in the Expressive Writing Intervention

Start date: February 2009
Phase: N/A
Study type: Interventional

The purpose of the present study is twofold. First, we will attempt to examine the role that emotion regulation and self-presentation play as potential moderators in the expressive writing paradigm. We hypothesize that expressive writing participants who demonstrate greater abilities to regulate their emotions at baseline will improve more on our outcome measures. We also hypothesize that those expressive writing participants who demonstrate higher levels of self-presentation at baseline will improve less on our outcome measures. The second aim of the study has two related objectives. First, we will attempt to investigate whether the expressive writing intervention can increase and enhance an individual's emotion regulation abilities. Related to this, we will then go on to examine whether emotion regulation can be looked at as a potential mechanism of action in the expressive writing procedure. Related to these two objectives, we hypothesize that in comparison to the control group, participants in the expressive writing condition will show increases in their ability to regulate their emotions from baseline to four week follow up. Moreover, we predict that greater gains in emotion regulation abilities for the expressive writing participants will be significantly related to greater gains in outcome measures.