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Stress Disorders, Traumatic clinical trials

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NCT ID: NCT00205517 Terminated - Depression Clinical Trials

Sedation and Psychopharmacology in Critical Care

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

Certain methods of sedation increase the duration of respiratory failure. Two strategies, a nursing- implemented sedation algorithm and daily interruption of sedatives, decrease length of mechanical ventilation compared to "conventional care" but have not been compared to each other. The reason certain methods of sedation lead to prolonged respiratory failure is unknown but may be related to altered pharmacokinetics and dynamics that are unique to critically ill patients. Critically ill patients receive substantial doses of sedatives over prolonged periods. The impact of these management strategies on short- and long-term psychiatric complications are unknown. The study seeks to test the central hypothesis that sedation practices impact strongly on outcome of respiratory failure and psychiatric complications. The three specific aims are (1) to compare two sedation strategies (protocol directed sedation and daily interruption of sedatives), (2) to examine the prevalence of psychiatric complications, and (3) to compute the pharmacokinetics of commonly used sedatives and narcotics. These aims will be achieved by enrolling critically ill patients in a prospective randomized trial comparing the above mentioned sedation strategies, and assessing sedation level as well as delirium throughout the duration of respiratory failure. Sedative plasma levels will be measured, and pharmacokinetics computed. Psychiatric morbidity will be assessed by administration of validated questionnaires.

NCT ID: NCT00204737 Completed - Clinical trials for Post-traumatic Stress Disorder

Short Course Glucocorticoid Treatment for PTSD

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

The purpose of this study is to investigate if a 2-wk course of 20mg/day of oral prednisone in addition to standard care will result in reduced PTSD symptoms or symptom severity compared to placebo

NCT ID: NCT00204386 Completed - Clinical trials for Posttraumatic Stress Disorder

Safety & Efficacy Study Using Topiramate in Posttraumatic Stress Disorder

Start date: September 2002
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study was to determine if Topiramate was safe and effective for use in civilian subjects with Posttraumatic Stress Disorder.

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: NCT00202449 Terminated - Clinical trials for Stress Disorders, Post-Traumatic

Prazosin vs Paroxetine in Combat Stress-Related Post-Traumatic Stress Disorder (PTSD) Nightmares & Sleep Disturbance

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

The purposes of this study are: - to evaluate the efficacy and tolerability of the drug prazosin compared to placebo for combat stress-related nightmares, sleep disturbance and overall function in recently combat-exposed returnees from Operation Iraqi Freedom (OIF) and Operation Enduring Freedom (OEF). - to evaluate the effects of the selective serotonin reuptake inhibitor (SSRI) paroxetine on behavioral symptoms and overall function in this population.

NCT ID: NCT00186511 Completed - Breast Cancer Clinical Trials

Expanding Rural Access: Distance Delivery of Support

Start date: November 2004
Phase: Phase 2
Study type: Interventional

The major goal of this project is to test the feasibility and acceptability of using videoconferencing to provide support groups led by trained facilitators to rural women with breast cancer in northern California.

NCT ID: NCT00186472 Completed - Depression Clinical Trials

Intervention to Decrease Anxiety in Parents of Infants in the Neonatal Intensive Care Unit (NICU)

Start date: n/a
Phase: N/A
Study type: Interventional

Infants born premature face numerous medical problems, causing significant anxiety for their parents. Parents experience a range of negative emotions including concern for the health and well being of their fragile infant, guilt, and disappointment. Research has indicated that having an infant in the Neonatal Intensive Care Unit (NICU) is highly stressful for parents and multiple studies have demonstrated that parents can develop significant psychological reactions to this experience. Specifically, many parents develop clinically significant anxiety disorders such as acute stress disorder (ASD) and posttraumatic stress disorder (PTSD). This not only impacts the mental well-being of the parents, but also can lead to problems with the parent-infant relationship, and, in turn, negatively impact the infant and the family as a whole. Despite the reported negative effects parents experience due to the stress of having an infant on the NICU, surprisingly little research has examined how to reduce parents' symptoms of anxiety. Because parents play an essential role in the care of their infant after discharge from the NICU, treating the parent's emotional distress is highly important. The purpose of this study is to examine the efficacy of a cognitive-behaviorally based intervention in reducing parents' symptoms of anxiety associated with having an infant on the NICU. This treatment is modeled after treatments that have proven effective with parents of children with other types of medical problems, for example, parents of children with cancer. It is the hope of the investigators that this intervention will effectively reduce symptoms of anxiety of NICU parents as well as the likelihood of developing subsequent psychological disorders.

NCT ID: NCT00186212 Completed - Breast Cancer Clinical Trials

Alternative Support for Rural and Isolated Women in an HMO

Start date: September 2000
Phase: Phase 3
Study type: Interventional

Evaluate the effects of a workbook/journal for helping isolated women to cope with breast cancer.

NCT ID: NCT00184418 Completed - Schizophrenia Clinical Trials

The Immune System and Psychiatric Disorders

Start date: January 2005
Phase: N/A
Study type: Observational

The study is based on a hypothesis that there is interaction between the activity in the immune system and in the mind. To study this, the investigators register different measures for activity in the immune system on patients unselectedly admitted to an acute psychiatric ward. The psychiatric statuses and diagnoses of these patients are carefully defined as well.