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Post-Traumatic Stress Disorder clinical trials

View clinical trials related to Post-Traumatic Stress Disorder.

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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: NCT00270959 Completed - Clinical trials for Post-Traumatic Stress Disorder

Patient-Centered Collaborative Care for Preventing Post-Traumatic Stress Disorder After Traumatic Injury

TSOS II
Start date: June 2006
Phase: Phase 1
Study type: Interventional

This study will evaluate the effectiveness of patient-centered collaborative care that combines behavioral therapy and drug therapy as compared to usual care in reducing symptoms of post-traumatic stress disorder in people who have survived a traumatic injury.

NCT ID: NCT00269490 Completed - Clinical trials for Post-Traumatic Stress Disorder

Yoga as a Therapy for Traumatic Experiences

Start date: December 2005
Phase: N/A
Study type: Observational

The purpose of the proposed research is to conduct a feasibility study of yoga as an adjunctive therapy for the treatment of posttraumatic stress disorder (PTSD) in 15 military personnel at the Walter Reed Army Medical Center (WRAMC) in Washington, DC. Participants will complete 10 weeks of yoga training, in addition to the continuing their usual and customary care for PTSD at WRAMC. The style of yoga chosen for this study, Yoga Nidra, uses deep relaxation, deep breathing and meditation to systematically reduce physical, emotional, mental, and even subconscious tension. After a diagnostic mental health assessment at baseline, participants will attend a total of 18 classes taught over a 10-week period and will practice daily at home using a compact disk provided by the instructor. Baseline measures will include the Patient Health Questionnaire, PD-HAT Trauma Questions, PTSD Symptom Scale - Interview, Fear of Loss of Vigilance Scale, and expectation of efficacy. The primary outcome measure will be the PTSD Checklist. Changes in health status, locus of control, and pain will be assessed over the course of the study. An additional goal of this study is to gather preliminary data on the anticipated effect size and feasibility of conducting a larger clinical study of the adjunctive use of yoga for the treatment of PTSD symptoms in enlisted military personnel.

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: NCT00248261 Terminated - Clinical trials for Post-traumatic Stress Disorder

Ziprasidone and Sertraline in PTSD

Start date: November 2005
Phase:
Study type: Observational

Serotonin re-uptake inhibitors, such as sertraline, are the medication of choice in post-traumatic stress disorder. However, it takes several weeks before they ameliorate symptoms. Therefore, we will add ziprasidone (vs. placebo) medication during the first four weeks of sertraline in order to find out if this strategy accelerates symptomatic relief.

NCT ID: NCT00245232 Completed - Clinical trials for Post-Traumatic Stress Disorder

Cognitive Processing Therapy Versus Its Individual Components in the Treatment of Post-Traumatic Stress Disorder and Depression in Women Who Have Been Sexually Abused

Start date: August 2000
Phase: N/A
Study type: Interventional

This study will evaluate the effectiveness of cognitive processing therapy versus its individual components in treating women with post-traumatic stress disorder (PTSD) and depression brought on by sexual assault.

NCT ID: NCT00239772 Completed - Clinical trials for Post-Traumatic Stress Disorder

Cognitive Processing Therapy Versus Prolonged Exposure for Treating Women With Post-Traumatic Stress Disorder Brought on by Sexual Assault

Start date: May 1994
Phase: N/A
Study type: Interventional

This study will evaluate the effectiveness of cognitive processing therapy versus prolonged exposure therapy in treating women with post-traumatic stress disorder (PTSD) brought on by sexual assault.

NCT ID: NCT00230893 Completed - PTSD Clinical Trials

Characterization of the Use of Antipsychotics in PTSD During the Past Seven Years

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

The primary objective is to examine the percentage of patients with PTSD who were prescribed an antipsychotic over the past seven years in the VA Network 7 (AL, GA, SC) and compare the percentage on an annual basis. We will also determine the type and dose of antipsychotics received. We hypothesize that there has been a significant increase in antipsychotic use, especially atypical antipsychotics, prescribed for patients with PTSD over the last 7 years

NCT ID: NCT00215241 Completed - Clinical trials for Post-Traumatic Stress Disorder

Risperidone Augmentation for PTSD

Start date: April 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to (1) compare the response of civilians with Posttraumatic Stress Disorder(PTSD) currently receiving sertraline without an optimal response to risperidone augmentation vs. placebo, and (2) to evaluate the tolerability of risperidone augmentation, and (3) to identifiy predictors of response to risperidone augmentation. the hypothesis is that risperidone augmentation of sertraline treatment of PTSD is safe and effective.