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Stress Disorders, Post-Traumatic clinical trials

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NCT ID: NCT00158262 Completed - Clinical trials for Post-Traumatic Stress Disorder

Effect of Propranolol on Preventing Posttraumatic Stress Disorder

Start date: September 2004
Phase: Phase 4
Study type: Interventional

This study will assess the effectiveness of taking propranolol soon after a traumatizing incident in reducing the incidence and severity of posttraumatic stress disorder in acutely traumatized individuals.

NCT ID: NCT00146900 Completed - Clinical trials for Post-traumatic Stress Disorder

Prevention of Post Traumatic Stress Disorder by Early Treatment

Start date: August 2004
Phase: N/A
Study type: Interventional

To prospectively evaluate the effect of early treatment (cognitive therapy (CT), cognitive-behavioral therapy (CBT) and escitalopram (SSRI) in preventing the occurrence of post-traumatic stress disorder in recent survivors of traumatic events.

NCT ID: NCT00136357 Completed - Clinical trials for Stress Disorders, Post-traumatic

Treatment of Posttraumatic Stress Disorder in Kosovar High School Students Using Mind-Body Skills Groups

Start date: August 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the participation in a group program which includes meditation, biofeedback, drawings, autogenic training, genograms, and a variety of movement and breathing techniques will decrease symptoms of posttraumatic stress in high school students.

NCT ID: NCT00133822 Completed - Clinical trials for Post-Traumatic Stress Disorders

Civilian Post-Traumatic Stress Disorder Risperidone Clinical Trial

Start date: April 2004
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether the administration of risperidone is effective in the treatment of selective serotonin reuptake inhibitor (SSRI)-resistant post-traumatic stress disorder (PTSD) in civilians.

NCT ID: NCT00131534 Completed - Clinical trials for Posttraumatic Stress Disorders

The Trauma Recovery and Resiliency Research Project

Start date: August 1991
Phase: N/A
Study type: Observational

The overall purpose of this study is the assessment of treatment outcome among traumatized patients seeking individual and/or group therapy at the Victims of Violence Program. The study gathers information from patients using quantitative (self-report) and qualitative (interview-based) approaches, to determine changes in symptom patterns and domains of functioning relevant to psychological trauma.

NCT ID: NCT00127673 Completed - Clinical trials for Post-Traumatic Stress Disorder

Comparison of Two Treatments for Post-Traumatic Stress Disorder

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

This study will compare the short- and long-term effectiveness of two different treatments for people with post-traumatic stress disorder.

NCT ID: NCT00127413 Completed - Pain Clinical Trials

Integrated Treatment for Chronic Pain and Posttraumatic Stress Disorder (PTSD)

Start date: September 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the efficacy of an integrated treatment for Veterans with comorbid chronic pain and posttraumatic stress disorder (PTSD). It is hypothesized that Veterans who receive the integrated treatment will report more positive outcomes than individuals who are assigned to treatment as usual, pain treatment, or PTSD treatment.

NCT ID: NCT00122109 Completed - Clinical trials for Posttraumatic Stress Disorder

Telemedicine and Anger Management Groups With PTSD Veterans in the Hawaiian Islands

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

Telemedicine has the potential to profoundly influence the delivery of specialized care to the remote veteran population suffering with PTSD. Preliminary research supports telemedicine technology as a possible solution to improve access to mental health services for veterans with PTSD. The proposed research is a treatment-outcome study that will assess the clinical efficacy of conducting an Anger Management Therapy (AMT) group treatment intervention using a videoteleconferencing (VTC) modality as compared to the traditional in-person modality with veterans who have PTSD and reside in remote locations on the Hawaiian Islands. AMT is a manual-guided cognitive-behavioral, skill based group intervention that has been used nationwide in VA substance abuse programs and most recently has been adopted by many VA PTSD Clinical Teams to treat anger-related to the sequelae of PTSD.

NCT ID: NCT00121888 Completed - Clinical trials for Stress Disorders, Post-Traumatic

Trial of Paroxetine-CR for the Treatment of Patients With Post Traumatic Stress Disorder Remaining Symptomatic After Initial Exposure Therapy

Start date: December 2002
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is to evaluate the effectiveness and tolerability of controlled-release paroxetine (Paxil-CR) compared to placebo (an inactive substance) for individuals who continue to have symptoms of post traumatic stress disorder (PTSD) despite receiving prolonged exposure therapy.

NCT ID: NCT00120627 Completed - Clinical trials for Stress Disorders, Post Traumatic

Mantram Repetition to Manage PTSD in Veterans

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

With ongoing war in Iraq, the incidence of posttraumatic stress disorder (PTSD) in combat veterans is increasing. Creation, implementation, and testing of new and innovative interventions are needed to provide additional options for enhancing the mental health of those with PTSD. Surveys indicate that veterans are interested in complementary approaches to health care. The purpose of this study is to determine the efficacy of the Mantram Repetition Program (MRP) delivered as a brief, 6-week, complementary and portable intervention. It includes frequent, silent repetitions of a mantram (mantra), a word or phrase with spiritual associations, to manage PTSD symptoms and improve quality of life military veterans with trauma.