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Posttraumatic Stress Disorder clinical trials

View clinical trials related to Posttraumatic Stress Disorder.

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NCT ID: NCT01324765 Completed - PTSD Clinical Trials

Women Overcoming and Managing Adversity Now (WOMAN) Study

WOMAN
Start date: January 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The goal of the study is to evaluate the efficacy of a two therapeutic models designed to enhance women's skills for managing reactive emotions in their current lives as well as to educate them about how using these skills can enhance their personal effectiveness and help them to gain control of post-traumatic stress reactions. The interventions adaptations of a manualized psychotherapy that has shown promise with adults with complex Posttraumatic Stress Disorder (PTSD) (Trauma Affect Regulation: Guide for Education and Therapy; TARGET) compared to a supportive group therapy (SGT) that has been found to have modest benefits with women survivors of childhood abuse (Wallis, 2002).

NCT ID: NCT01314612 Enrolling by invitation - Insomnia Clinical Trials

Initial Study of Insomnia/Nightmare Group Treatment for Posttraumatic Stress Disorder (PTSD)

Start date: March 2011
Phase: N/A
Study type: Interventional

Many combat Veterans suffer from posttraumatic stress disorder (PTSD), an anxiety disorder that develops after an extremely stressful event or events. PTSD is associated with problems falling asleep or staying asleep. Veterans with PTSD also commonly have nightmares from stressful experiences. These symptoms can cause problems in daily life. Behavioral treatments that do not involve taking medication have been shown to help improve problems related to sleep and nightmares. However, very few of these treatments address both sleep problems and nightmares at the same time, even though many people suffer from both problems. The purpose of this study is to examine the effectiveness of a combined treatment for sleep problems and nightmares in Veterans suffering from combat-related PTSD that is presented in a group format. The investigators hypothesize that the completion of this treatment will lead to increases in sleep quality and decreases in the frequency and severity of nightmares as measured by standard questionnaires.

NCT ID: NCT01307475 Terminated - Clinical trials for Posttraumatic Stress Disorder

Study of Quality of Life in Freeman-Sheldon Syndrome and Related Conditions

FSS-QLS
Start date: February 2011
Phase: N/A
Study type: Observational

Freeman-Sheldon syndrome (FSS) is a rare human neuromusculoskeletal disorder present before birth, involving primarily limb and craniofacial deformities. The hypotheses in the present study of FSS and related conditions are: (1) FSS and related conditions are associated with higher rates of posttraumatic stress symptoms (PTSS), depression, and reduced quality of life than is observed in the general population; (2) persons close to an individual with FSS or related condition suffer similarly; and (3) current measures, which are single-disease specific (i.e., PTSS, depression, craniofacial deformities, or limb deformities), do not capture the unique picture of FSS and related conditions, which involve both limb and craniofacial deformities in an intellectually capable individual. There have been no studies looking at quality of life associated with FSS. Some authors have looked at quality of life in persons with facial differences; other authors have looked at bone and joint problems. Many other authors have looked at PTSS and depression caused by health problems and bad medical experiences. No authors have looked at these problems when they happen together, as they do in FSS. Because of the above, there may be differences in patients that have FSS versus patients in previous quality of life studies. The study will also develop and validate an outcomes-based quality of life survey for FSS and related conditions.

NCT ID: NCT01306136 Completed - Clinical trials for Posttraumatic Stress Disorder

Pilot Study of Exposure Therapy for Posttraumatic Stress Disorder

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

The purpose of this project is to examine the feasibility of a culturally adapted, manual based Prolonged Exposure therapy intervention for the treatment of Spanish-speaking Puerto Ricans with posttraumatic stress disorder

NCT ID: NCT01304940 Completed - Clinical trials for Posttraumatic Stress Disorder

Women's Post Traumatic Stress Disorder (PTSD) Research Study

Start date: December 1, 2008
Phase:
Study type: Observational

The purpose of this study is to examine the relationship between trauma and startle. The investigators are also looking at the effect of menstrual phase on this relationship.

NCT ID: NCT01286415 Completed - Clinical trials for Posttraumatic Stress Disorder

Group Cognitive Processing Therapy for Combat-related Posttraumatic Stress Disorder (PTSD)

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

The purpose of this study is to compare group-administered Cognitive Processing Therapy-Cognitive-only version (CPT-C), an evidence based treatment for posttraumatic stress disorder (PTSD), to Present Centered Therapy (PCT) in order to determine whether the results of CPT exceed those of receiving a therapy that focuses on current problems rather than past trauma in a group format.

NCT ID: NCT01274741 Completed - Clinical trials for Alcohol Use Disorder

Present- Versus Past-focused Therapy for PTSD and Substance Use Disorder

Start date: January 2011
Phase: N/A
Study type: Interventional

This study compares Creating Change, a new past-focused behavioral therapy for posttraumatic stress disorder (PTSD)/substance use disorder (SUD), to Seeking Safety, an evidence-based present-focused behavioral therapy for PTSD/SUD.

NCT ID: NCT01263067 Completed - Clinical trials for Posttraumatic Stress Disorder

Lifespan Integration for Posttraumatic Stress Disorder From an Auto Accident

Start date: October 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate if lifespan integration (LI) therapy reduces posttraumatic stress symptoms following a motor vehicle accident (MVA) trauma

NCT ID: NCT01259921 Completed - Clinical trials for Posttraumatic Stress Disorder

EEG Biofeedback in the Treatment of Chronic Treatment-Resistant PTSD

Start date: December 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether neurofeedback (NF) training can significantly reduce the symptoms of Posttraumatic Stress Disorder (PTSD) in individuals with significant affect dysregulation and chronic, treatment-resistant PTSD. The primary aims of this study include: 1. To examine whether NF has the potential to significantly reduce symptoms of PTSD. 2. To examine whether NF training can specifically target the area of affect regulation. 3. To examine the mechanism of NF through elucidating the relationship between affect regulation and PTSD symptom change.

NCT ID: NCT01239173 Terminated - Clinical trials for Posttraumatic Stress Disorder

Emotional Memory Reactivation in Posttraumatic Stress Disorder

VIVITRAU
Start date: September 2010
Phase: Phase 3
Study type: Interventional

Converging lines of evidence have implicated the amygdala in the pathophysiology of posttraumatic stress disorder. The primary purpose of our study is to assess the effect of propanolol, a beta adrenergic antagonism, on amygdala activation during a symptom provocation state in traumatized subjects with and without posttraumatic stress disorder.