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Stress Disorders, Post-Traumatic clinical trials

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NCT ID: NCT00333710 Completed - Hepatitis C Clinical Trials

Evaluating a Telehealth Treatment for Veterans With Hepatitis C and PTSD

Start date: September 2006
Phase: N/A
Study type: Interventional

The main objective of this proposal is to develop and test the efficacy of two interventions (a telehealth and face-to-face intervention) designed to improve quality of life, self-care, motivation to engage in healthcare, and psychological distress in patients diagnosed with HCV and PTSD. It is hypothesized that

NCT ID: NCT00329992 Completed - Clinical trials for Chronic Posttraumatic Stress Disorder

Brief Eclectic Psychotherapy for PTSD - a Randomized Controlled Trial

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

Participants are randomly assigned to either 16 sessions of Brief Eclectic Psychotherapy (Gersons et al. (2000) Journal Trauma Stress 13: 333-348), comprising psychoeducation, exposure, mementos and writing assignments, domain of meaning and integration, farewell ritual, or a minimal attention control group that will be offered 16 sessions of BEP after a waiting time of four months. Participants in the minimal attention control group receive monthly telephone calls and complete a symptom self monitoring diary (Tarrier, N. et al. (1999) Behavior Therapy 30: 597-605) for three weeks.

NCT ID: NCT00320138 Completed - Clinical trials for Posttraumatic Stress Disorder (PTSD)

Acupuncture for the Treatment of Posttraumatic Stress Among Military Personnel

Start date: March 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the effectiveness of acupuncture as a treatment for Posttraumatic Stress Disorder (PTSD) among military personnel.

NCT ID: NCT00306540 Completed - Clinical trials for Post-Traumatic Stress Disorder

Use of Quetiapine as an Add on Therapy in the Treatment of Post Traumatic Stress Disorder

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

The purpose of this study is to evaluate how effective quetiapine versus placebo is when added to an existing therapy, in reducing the symptoms of PTSD.

NCT ID: NCT00300313 Completed - Clinical trials for Post-traumatic Stress Disorder

PTSD Prevention Using Escitalopram

Start date: June 2005
Phase: N/A
Study type: Interventional

Assessing the efficacy of escitalopram in preventing the development of PTSD, or or reducing its severeness, after exposure to a traumatic event.

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: NCT00292370 Completed - Clinical trials for Stress Disorders, Post-Traumatic

Quetiapine Augmentation for Treatment-resistant PTSD

Start date: January 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the response of veterans with PTSD without an optimal response to paroxetine to quetiapine augmentation versus placebo.

NCT ID: NCT00290225 Completed - Depression Clinical Trials

Yoga Breath Program and Client-Centered Exposure for Relief of PTSD in Tsunami Victims

Start date: June 2005
Phase: Phase 3
Study type: Interventional

Study hypothesis: that a standardized course of Eastern practices (Breath Water Sound Course -BWS) will significantly relieve PTSD and depression in tsunami victims. Further, that a client-centered exposure treatment (Traumatic Incident Reduction- TIR) would provide additional, significant relief of PTSD and depression in tsunami victims. 180 tsunami victims in Southern India will be divided into three groups: those that only receive BWS course, those that receive the BWS course and TIR and a wait-list control. They will be pretested with the PCL-17 (PTSD scale), the Beck Depression Inventory and the General Health Questionaire. These scales will also be administered post-service as well as five weeks post pre-testing and at three and six month intervals.

NCT ID: NCT00288860 Completed - Clinical trials for Stress Disorders, Post-Traumatic

Telephone Case Monitoring (TCM) for Veterans With Post-Traumatic Stress Disorder (PTSD)

TCM-PTSD
Start date: October 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to test whether providing PTSD patients additional support by telephone (in addition to usual outpatient care) after they discharge from residential treatment improves those patients' outcomes and keeps them out of the hospital longer.

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.