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Post-Traumatic Stress Disorders clinical trials

View clinical trials related to Post-Traumatic Stress Disorders.

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NCT ID: NCT00908882 Completed - Clinical trials for Tobacco Use Cessation

Tobacco Cessation for Veterans With Post Traumatic Stress Disorder (PTSD)

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

The goal of this study is to improve the effectiveness of tobacco cessation treatment for veterans with Post Traumatic Stress Disorder (PTSD) through ongoing, integrated care management approach using telehealth and motivational interviewing counseling. Both tobacco dependence and PTSD represent enormous challenges to the Veterans Affairs (VA) healthcare system.

NCT ID: NCT00893568 Completed - Clinical trials for Post Traumatic Stress Disorders

Post Traumatic Stress Disorder and Neural Mechanisms Involved in Its Treatment

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

The post traumatic stress disorder PTSD arises when the physiological response to stress does not come to its term. This study aims to explore the cognitive, psycho physiological and cerebral mechanisms involved in PTSD, in fear conditioning and face matching tasks, before and after treatment.PTSD patients will be recruited by Pr Jean-Claude Samuelian in his service at the Conception Hospital and by Pr Jean-Michel Azorin in his service at the Sainte Marguerite Hospital (Marseille) and will undergo either CBT or EMDR within those same services. The tasks they will be asked to perform will study the psycho physiological, cognitive and central mechanisms involved in PTSD and its treatment. All in all, 17 healthy controls will be recruited as well as 17 PTSD patients for each of the two treatment group.In terms of perspectives, this study would help isolate neural systems functionally involved in PTSD and its treatment. A better knowledge of those mechanisms would set room for the optimization of the current PTSD treatment.

NCT ID: NCT00827879 Completed - Aggression Clinical Trials

Strength at Home Couples Program (PTSD-Focused Relationship Enhancement Therapy for Returning Veterans)

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

The purpose of the project is to develop and test a couples-based relationship enhancement group intervention for married or partnered Operation Enduring Freedom (OEF)/Operation Iraqi Freedom (OIF)/Operation New Dawn (OND) veterans to prevent the perpetration of intimate partner aggression (IPA) among participants.

NCT ID: NCT00778960 Completed - Clinical trials for Post-Traumatic Stress Disorders

Mechanistic Pathways of Mindfulness Meditation in Post-traumatic Stress Disorder.

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

The purpose of this study is to find out how meditation influences certain systems in the body: nervous system, hormonal system, and respiratory system. Another purpose is to see how meditation may help improve post-traumatic stress disorder symptoms.

NCT ID: NCT00723008 Completed - Burns Clinical Trials

Cranial Electrotherapy Stimulation in Burned Patients

CES
Start date: May 2007
Phase: Phase 2
Study type: Interventional

To find out if Cranial Electrotherapy Stimulation is a useful treatment for people who have been burned and have Post Traumatic Stress Disorder. CES may be helpful in giving relief to some or all of those symptoms.

NCT ID: NCT00564317 Completed - Clinical trials for Post-Traumatic Stress Disorders

KIDNET vs Meditation/Relaxation - a Dissemination Randomized Controlled Trial for the Treatment of Traumatized Children After War in Sri Lanka

Start date: September 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the efficacy of KIDNET versus a Meditation/Relaxation protocol in treating traumatized children when applied by locally trained teacher counsellors as well as the effectiveness and adequacy of such a treatment in a south-asian war affected stayee child community.

NCT ID: NCT00350584 Completed - Clinical trials for Post Traumatic Stress Disorders

Evaluation of Telehealth Interventions for Post-Trauma Stress

Start date: February 2007
Phase: N/A
Study type: Interventional

Posttraumatic Stress Disorder (PTSD) is very prevalent within the veteran population and is associated with decreased quality of life and an increased risk of developing other psychiatric and physical illnesses. The overarching objective of the proposed study is to evaluate the effectiveness of two telehealth treatment conditions in promoting healing within a population of veterans with full or partial PTSD. In particular, we are targeting newly returned veterans from the Iraq and Afghanistan conflicts. Specifically, we are comparing the relative efficacy of an alternative therapeutic approach, a Mindfulness based treatment, with a Psychoeducation treatment in reducing symptoms of PTSD and more generalized psychiatric symptoms, while increasing quality of life. Of note, both treatment conditions will consist of two in-person sessions and six brief weekly telephone calls. Participants will be 58 veterans (29 per condition) recruited from the VA Boston Healthcare System. Assessment will occur before and after the delivery of the intervention. We hypothesize that while both treatments will result in improved outcomes, the Mindfulness intervention will promote more healing than the Psychoeducation intervention. Results from this project will help further our understanding of the role of mindfulness in treating PTSD, particularly in those veterans who are returning from deployment.

NCT ID: NCT00294970 Completed - Clinical trials for Obsessive-Compulsive Disorder

Cognitive Characteristics of PTSD Patients With OCD

Start date: February 2006
Phase: N/A
Study type: Observational

Cognitive profile of patients who suffer both from PTSD and OCD, as compared to those who suffer from PTSD or OCD without other comorbidity.

NCT ID: NCT00288314 Completed - Anxiety Clinical Trials

fMRI in Posttraumatic Stress Disorder (PTSD) During Working Memory Updating

METRAPI
Start date: January 2007
Phase: N/A
Study type: Observational

Neuropsychological studies investigating trauma-exposed and posttraumatic stress disorder (PTSD) subjects have generally underlined the significantly poorer performance of tasks that require attention, concentration, and verbal memory, and difficulty in regulating memories surrounding the traumatic event. A previous study (El Hage et al. Cognitive Neuropsychiatry, 2006) revealed that the trauma-exposed subjects scored higher on anxiety/depression scales, and lower on processing speed tests. Moreover, the study showed significant impairment in working memory partially mediated by speed processing, but not by anxiety or depression. These results suggest that processing speed makes a major contribution to trauma-related working memory decline, and needs to be investigated in further studies.The aim of the present study is to explore correlation between hippocampus volume, frontal dysfunction and cognitive slowing in trauma-exposed subjects, while examining brain activation during performance of working memory tasks using functional magnetic resonance.

NCT ID: NCT00227357 Completed - HIV Infections Clinical Trials

The CORE Buprenorphine Project - An HIV Primary Care Program Demonstration

BUP
Start date: July 2005
Phase: N/A
Study type: Observational

The goal of this study is to develop and evaluate an innovative model of care to better serve patients who are both HIV-infected and opioid-dependent.