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Stress Disorders, Traumatic clinical trials

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NCT ID: NCT00353938 Completed - Clinical trials for Posttraumatic Stress Disorder

Study of 3,4-Methylenedioxymethamphetamine-assisted Psychotherapy in People With Posttraumatic Stress Disorder

Start date: September 13, 2006
Phase: Phase 2
Study type: Interventional

This study will examine MDMA-assisted psychotherapy in individuals aged 18 years or older diagnosed with PTSD, with PTSD symptoms not improving after trying at least one treatment. This objective of this study is to determine whether three eight-hour long sessions of MDMA-assisted psychotherapy, scheduled three to five weeks apart, can be safely administered to participants with PTSD, and whether combining a fully therapeutic dose of MDMA with psychotherapy, when compared with a low ("active placebo") dose of MDMA, will reduce PTSD symptoms. Participants will be randomly assigned to receive the full dose of MDMA (125 mg) or assigned to receive a low or "active placebo" dose of MDMA (25 mg) during each of three experimental sessions.

NCT ID: NCT00353249 Completed - Clinical trials for Post-Traumatic Stress Disorder

Cognitive Behavioral Therapy for Post-Traumatic Stress Disorder in Homeless Women

Start date: June 2008
Phase: Phase 1
Study type: Interventional

This study will determine the effectiveness of cognitive behavioral therapy in treating post-traumatic stress disorder in homeless women.

NCT ID: NCT00352469 Completed - Anxiety Disorders Clinical Trials

Trial of Seroquel SR for Alcohol Dependence and Comorbid Anxiety

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

Alcohol use disorders (AUDs) are a major problem facing our society. Their treatment is complex, and involves multiple behavioral and pharmacotherapy interventions. There are 3 approved medications for AUDs, but their efficacy for AUDs that co-exist with anxiety disorders is unknown. This study explores the effects of the medication, sustained-release quetiapine fumarate (Seroquel SR) for the treatment of alcohol dependence and co-morbid anxiety. Primary outcome measure is the amount of alcohol used. Secondary outcome measures include craving for alcohol, length of sobriety from drinking and level of anxiety with Seroquel SR.

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: NCT00348036 Completed - Depression Clinical Trials

Group Intervention for Interpersonal Trauma

Start date: September 2008
Phase: N/A
Study type: Interventional

This study will assess the acceptability and effectiveness of a six-session, modular, repeating group for low-income women who have symptoms of depression and/or post-traumatic stress disorder following interpersonal trauma exposure.

NCT ID: NCT00347269 Completed - Clinical trials for Post-traumatic Stress Disorder

Primary Care Intervention Strategy for Anxiety Disorders

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

This study will compare the effectiveness of an intervention strategy for the treatment of people with post traumatic stress disorder, generalized anxiety disorder, panic disorder, and social anxiety disorder in the primary care setting.

NCT ID: NCT00333801 Completed - Clinical trials for Posttraumatic Stress Disorder (PTSD)

The Impact of Vocational Rehabilitation on Mentally III Veterans

Start date: April 1, 2006
Phase: N/A
Study type: Interventional

To study the impact of Individual Placement and Support (IPS) supported employment (SE) compared to treatment-as-usual vocational rehabilitation program (VRP) for veterans with posttraumatic stress disorder (PTSD).

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.