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Stress Disorders, Post-Traumatic clinical trials

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NCT ID: NCT00611338 Completed - HIV Infections Clinical Trials

Efficacy of Group Intervention to Reduce Stress Symptoms

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

This research study will examine the usefulness of groups in reducing stress and helping individuals with HIV to stay healthy and avoid problems associated with sexually transmitted diseases. We hope to discover whether being in a group is effective in reducing stress-related symptoms and promoting healthy behaviors.

NCT ID: NCT00607412 Completed - PTSD Clinical Trials

Alcohol Use Disorders (AUDs) and Post-traumatic Stress Disorder (PTSD) Treatment for Victims of Partner Violence

Start date: August 2007
Phase: Phase 2
Study type: Interventional

The goal of this study is to evaluate a psychotherapy for PTSD and substance use disorders among women who have experienced domestic violence. The hypothesis is that women who receive present-focused, integrated treatment will have greater PTSD symptom reduction and have less substance use after treatment than women in the control condition who will receive supportive therapy based on a 12-step approach.

NCT ID: NCT00604045 Completed - Clinical trials for Stress Disorders, Post-Traumatic

DoD PTSD November 13 - Information Processing Modification in the Treatment of PTSD

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

The purpose of this study is to determine whether a computerized intervention designed to change the nature of attention biases will be effective in reducing the symptoms of post traumatic stress disorder (PTSD) in American combat veterans returning from the wars in Afghanistan and Iraq.

NCT ID: NCT00602732 Completed - Depression Clinical Trials

Interpersonal Treatment Program to Prevent Depression and Post-Traumatic Stress Disorder in Low-Income Pregnant Women With Partner Abuse

Start date: September 2005
Phase: Phase 1
Study type: Interventional

This study will evaluate the effectiveness of an interpersonally oriented treatment program called Reach Out for a Safe Environment in preventing depression and post-traumatic stress disorder in low-income pregnant women who have experienced recent partner abuse.

NCT ID: NCT00602069 Completed - Clinical trials for Post-Traumatic Stress Disorder

Cognitive Behavioral Therapy for Treating Recently Abused Women With Post-Traumatic Stress Disorder

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

This study will evaluate the effectiveness of a brief cognitive behavioral treatment, Helping to Overcome PTSD through Empowerment, in treating abused women with post-traumatic stress disorder who are living in shelters.

NCT ID: NCT00601952 Completed - Clinical trials for Stress Disorders, Post-traumatic

Information Processing Modification in PTSD (Oct. 18)

Start date: July 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a computerized intervention designed to change the nature of attention biases will be effective in reducing the symptoms of post traumatic stress disorder (PTSD) in American combat veterans returning from the wars in Afghanistan and Iraq.

NCT ID: NCT00600418 Completed - Clinical trials for Stress Disorders, Post-Traumatic

Identifying Toddlers and Their Parents Who Are Suffering From Posttraumatic Distress Following War and Terror

Start date: April 2007
Phase: Phase 0
Study type: Observational

The project is aimed at identifying children who are suffering from posttraumatic distress and increasing capacity to provide treatment for them and for their caretakers. The project will be implemented in 3 cities in Israel, Haifa, Kiryat Shmona and Sderot, exposed to terrorism and the effects of war

NCT ID: NCT00599599 Unknown status - HIV Infections Clinical Trials

Stress-Reducing Interventions in HIV+ Patients: Pilot

PEACH
Start date: April 2005
Phase: N/A
Study type: Interventional

The primary aim of this project is to examine the efficacy of prolonged exposure (PE) therapy at reducing HIV-related PTSD symptoms, increasing adherence to antiretroviral medication regimens, and increasing health-related quality of life (QOL) in HIV+ patients.

NCT ID: NCT00597857 Recruiting - Clinical trials for Posttraumatic Stress Disorder

Prevention of Posttraumatic Stress Disorder (PTSD) With Early Hydrocortisone Treatment: Pilot

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

People experience a wide range of outcomes following a traumatic event. Although rates differ depending on type of trauma, 20-60% of trauma victims may develop posttraumatic stress disorder (PTSD). However, not all trauma victims develop PTSD. Previous research has found that trauma victims who develop PTSD excrete lower levels of urinary cortisol immediately after a trauma than victims who do not develop PTSD. Other research has suggested that increasing levels of cortisol may protect against the development of PTSD in patients such as yourself- but this has not yet been examined. Cortisol is a naturally occurring hormone in your body, and the present study is designed to test whether increasing cortisol levels can protect against or decrease symptoms of PTSD. Participants in this study will be randomly assigned to one of two treatment groups. Participants will receive either hydrocortisone (20mg, twice per day) or a placebo (a sugar pill) for 10 days with a six-day taper. There is an equal chance of being in either treatment group, and neither the participant nor the experimenters will know which treatment was received (except in case of an emergency).

NCT ID: NCT00597389 Completed - Clinical trials for Posttraumatic Stress Disorders

Propranolol Administration and Prevention of Child PTSD in Child Trauma Victims

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

Twenty-nine pediatric injury patients (ages 10-18) at risk for PTSD were randomly assigned to receive either propranolol or placebo in a double-blind placebo controlled design. Medication was initiated within 12 hours of hospital admission. At 6-weeks, child PTSD symptoms and heart rate (HR) during trauma recall were assessed. We hypothesized that participants who received propranolol would report fewer PTSD symptoms and have lower heart rates than those who received placebo.