Clinical Trials Logo

PTSD clinical trials

View clinical trials related to PTSD.

Filter by:

NCT ID: NCT00208208 Completed - PTSD Clinical Trials

Geodon (Ziprasidone) for Posttraumatic Stress Disorder

Start date: December 2002
Phase: Phase 4
Study type: Interventional

Atypical antipsychotics have shown promise in the treatment of depression and anxiety, which are prominent symptoms of PTSD. The profile of the atypical antipsychotic, ziprasidone (Geodon), suggests possible anxiolytic and antidepressant properties. This research will assess the potential effectiveness of Geodon in civilian men and women who suffer from severe PTSD. Response to ziprasidone or placebo will be measured by Clinician Administered PTSD Scale (CAPS) and Treatment Outcomes PTSD Scale (TOP-8).

NCT ID: NCT00203463 Completed - PTSD Clinical Trials

Topiramate in the Treatment of Post Traumatic Stress Disorder (PTSD)

Start date: July 2001
Phase: Phase 4
Study type: Interventional

To study the potential therapeutic effects of topiramate (Topamax) in the treatment of PTSD.

NCT ID: NCT00203385 Terminated - PTSD Clinical Trials

Maintenance Phase Treatment With Divalproex for Post Traumatic Stress Disorder

Start date: May 2003
Phase: Phase 4
Study type: Interventional

The primary objective is to evaluate the long-term efficacy of divalproex sodium (Depakote) in the continuation treatment of PTSD.

NCT ID: NCT00202709 Completed - PTSD Clinical Trials

Can Thought Field Therapy (TFT) be Helpful for Patients With an Anxiety Disorder?

Start date: May 2002
Phase: N/A
Study type: Interventional

The purpose of this study is to find out if Thought Field Therapy has effect on certain anxiety disorders; agoraphobia, social phobia, and post traumatic stress disorder (PTSD).

NCT ID: NCT00186030 Terminated - HIV Clinical Trials

Reducing Risk and Trauma-Related Stress in Persons Living With HIV

Start date: April 2003
Phase: Phase 1/Phase 2
Study type: Interventional

This two-year study tested the concept that an intervention, which reduces trauma-related symptoms among adults who are living with human immunodeficiency virus (HIV), are experiencing trauma-related stress symptoms, and engaging in behavior that facilitates HIV transmission, can reduce the transmission risk of (HIV). Our central premise was that by first treating trauma symptoms, we would enhance the effects of a skills-building HIV risk reduction intervention for adults experiencing trauma-related symptoms such as hyperarousal, dissociation, and avoidance. The study aims were to: 1. To determine if decreasing trauma-related stress symptoms improves HIV risk reduction behavior above a standard HIV risk reduction intervention alone post-intervention and 3 months after the small group intervention sessions; 2. To determine whether key variables moderate the intervention’s effects. For instance, gender, age, ethnicity, or psychological distress (e.g., depression, anxiety) may interact with the intervention to affect risky sexual or drug-related behavior; and 3. To determine whether there is evidence that the theoretical mediator variables, which include trauma-related stress symptoms, self-efficacy, communication skills, and social support mediate the intervention’s effects on outcomes. This information addresses the theoretical question of why the intervention works.

NCT ID: NCT00108576 Completed - PTSD Clinical Trials

Divalproex Sodium in the Treatment of PTSD (Post-Traumatic Stress Disorder)

Start date: October 2003
Phase: Phase 3
Study type: Interventional

The purposes of this study are: - To study the efficacy of divalproex in the treatment of PTSD; - To study the plasma GABA (gamma aminobutyric acid) levels before and after treatment with divalproex in PTSD.

NCT ID: NCT00105820 Completed - PTSD Clinical Trials

Evaluation Study of TIDES Depression Care Quality Improvement Intervention

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

In spite of the impact on veteran�s health status and treatment cost, depression is under-diagnosed and under-treated. The goal of this study is to learn how to implement a previously tested, effective collaborative care model for improving the quality of depression care across multiple Veterans Integrated Service Networks (VISNs). To achieve this goal, we are conducting a randomized controlled trial of evidence-based quality improvement (EBQI), a dissemination method that relies on expert design and local implementation of evidence-based practice interventions. We hypothesize that EBQI will result in increased rates of assessment and appropriate management of depression. Results will be useful in designing realistic chronic care programs and performance measures for continuing care improvement.

NCT ID: NCT00018798 Completed - PTSD Clinical Trials

Post-Traumatic Stress Disorder (PTSD) Symptom Study

Start date: April 1, 2000
Phase:
Study type: Observational

The primary goals for this investigation are to quantify: (1) fluctuations in PTSD symptom reports when assessed at bi-weekly intervals; (2) change in PTSD symptoms associated with stressful life events; and (3) change in PTSD symptoms associated with perceived social support.

NCT ID: NCT00013091 Completed - Depression Clinical Trials

Treatment of Depression in Patients With PTSD

Start date: October 1997
Phase: N/A
Study type: Interventional

Post-traumatic stress disorder is a mental health problem of enormous proportion within the VA system for both male and female veterans. The 40 percent of veterans with PTSD and concurrent clinically significant depression are particularly difficult to treat. Effective and efficient treatment of veterans with this combination of disorders would be of benefit to a significant number of veterans.