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Stress Disorders, Traumatic clinical trials

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NCT ID: NCT00978484 Active, not recruiting - Clinical trials for Post Traumatic Stress Disorder

A Head-to-head Comparison of Virtual Reality Treatment for Post Traumatic Stress Disorder

Start date: September 2009
Phase: Phase 3
Study type: Interventional

Therapy that uses Virtual Reality (VR) has been shown to help in the treatment of Post Traumatic Stress Disorder (PTSD). It is unclear what role the VR simulator itself plays in recovery. This study is examining if full-immersion in VR causes greater improvement in PTSD symptoms than does similar therapy that uses a simple, static, computer image.

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.

NCT ID: NCT00725192 Active, not recruiting - Clinical trials for Posttraumatic Stress Disorder

Sleep-directed Hypnosis As A Complement To Cognitive Processing Therapy (CPT) In Treating Posttraumatic Stress Disorder (PTSD)

Hypnosis
Start date: July 2008
Phase: N/A
Study type: Interventional

Sleep impairment is the most often reported of the 17 PTSD symptoms and is considered one of the most refractory to treatment. This study proposes the use of sleep-directed hypnotherapy to address sleep issues as a complementary element to empirically supported Cognitive Processing Therapy (CPT) in treating PTSD in sexual and physical assault survivors. Specifically the study aims to: 1) compare the results of sleep-directed hypnosis plus CPT with CPT only, 2) to assess the relationship between sleep and PTSD symptoms, 3) to examine relationships between sleep improvement, PTSD symptom improvement, and the therapeutic elements (hypnosis, exposure, cognitive therapy) to determine mechanisms of action in the intervention, 4) to assess the relationship between sleep and physical reactivity to trauma-related cues and to other stimuli.

NCT ID: NCT00657787 Active, not recruiting - Clinical trials for Stress Disorders, Post-Traumatic

Development of a Post-Traumatic Stress Disorder (PTSD) Population Registry for Veterans

Start date: September 2008
Phase:
Study type: Observational

The overall objective of this project is to develop the first longitudinal registry of combat-exposed men and women with PTSD. This registry will provide essential data on the natural history, including progression and remission, and outcomes associated with PTSD in military service men and women who have utilized the Department of Veterans Affairs (VA) health care system. Additional goals of this project are to determine risk factors for PTSD among combat-exposed service men and women (by incorporating a combat-exposed non-PTSD group of veterans into analyses), and to assess the joint effects of combat exposure and PTSD on a broad range of outcome measures (by incorporating a non-combat-exposed group of veterans into analyses). Thus, the registry will allow an evaluation of current theoretical models of symptom development and progression in a large sample of service men and women who utilize the VA medical system. In addition to the PTSD registry, we will collect information on two comparison groups of OIF/OEF-era veterans to conduct nested case control studies within the general VA health care utilization database. First, a comparison group of combat veterans who are high utilizers of VA medical care, but who have not received a diagnosis of PTSD will be identified. This group will be used in analyses to identify risk factors for PTSD. Additionally, the rate of PTSD symptoms will be evaluated in this comparison group to estimate the prevalence of missed PTSD diagnoses among combat veterans with high rates of service utilization, and the resulting impact on utilization and outcomes. A second comparison group will consist of veterans with similar service record and demographic backgrounds, who were not deployed to the OIF/OEF war zones. Thus, the proposed project will create a PTSD registry from the VA database to assess the natural history and progression of PTSD in combat veterans from OIF/OEF and also to conduct case-control studies nested within the VA database. The case-control comparisons will be used to evaluate key hypotheses related to the specific aims of the overall project.

NCT ID: NCT00481000 Active, not recruiting - Clinical trials for Posttraumatic Stress Disorder

Dialectical Cognitive Traumatherapy (DCT) on Patients With Severe PTSD Following Sexual Abuse

PASA
Start date: April 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether Dialectical Cognitive Traumatherapy is effective in the treatment of severe and chronic Posttraumatic Stress Disorder (PTSD) following childhood sexual abuse.

NCT ID: NCT00431847 Active, not recruiting - Anxiety Disorders Clinical Trials

Regional Anesthesia Military Battlefield Pain Outcomes Study

RAMBPOS
Start date: October 2007
Phase: N/A
Study type: Observational

The purpose of this study is to examine the short and long-term benefits of implementing early regional anesthesia techniques for pain control after a major traumatic injury to one or more extremities during combat in the Iraqi/Afghanistan war, including the effects on acute and chronic pain, quality of life, and mental health.

NCT ID: NCT00269451 Active, not recruiting - Clinical trials for Post-Traumatic Stress Disorder

Assessing PTSD After Earthquake in Turkey

Start date: n/a
Phase: N/A
Study type: Observational

Assessing the prevalence and natural course of PTSD after the 1999 Turkish earthquake

NCT ID: NCT00174551 Active, not recruiting - Clinical trials for Stress Disorders, Post-Traumatic

Feasibility Study: The Effect of Prazosin for Nighttime Symptoms of Civilian PTSD

Start date: November 2003
Phase: N/A
Study type: Interventional

Investigating the effect of prazosin for nighttime symptoms of civilian Posttraumatic Stress Disorder.