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Stress Disorders, Post-Traumatic clinical trials

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NCT ID: NCT02372396 Completed - Clinical trials for Posttraumatic Stress Disorder

Compassion Meditation for PTSD

Start date: February 2015
Phase: N/A
Study type: Interventional

The goal of this project is to refine an existing compassion meditation protocol for individuals with posttraumatic stress disorder (PTSD), to examine the safety and feasibility of this approach and to collect data to make initial estimates of efficacy.

NCT ID: NCT02370576 Not yet recruiting - Clinical trials for Depressive Disorder, Major

The Effect of Traumatic Childbirth on the Incidence of PTSD and Other Major Postpartum Psychopathology

Start date: March 2015
Phase: N/A
Study type: Observational [Patient Registry]

Determination of incidence and prevalence of PTSD and other types of psychopathology (such as anxiety and affective disorders) after traumatic birth experiences and elucidation of salient risk factors in the local population sample- by prospective follow-up.

NCT ID: NCT02369614 Terminated - Clinical trials for PTSD - Post Traumatic Stress Disorder

Low -vs- High-Frequency Repetitive TMS of the Right Dorsolateral Prefrontal Cortex in PTSD

Start date: August 2014
Phase: N/A
Study type: Interventional

This is a randomized placebo/sham controlled, double-blind study investigating the efficacy of high- and low-frequency rTMS applied to the right DLPFC at either 1 Hz, 10 Hz, or sham rTMS as compared to an OASIS treatment as usual group for the treatment of PTSD symptoms.

NCT ID: NCT02368444 Completed - Clinical trials for Stress Disorders, Post-Traumatic

A Cognitive Behavioral Therapy and Yoga Program for Trauma Symptoms

Start date: May 2014
Phase: N/A
Study type: Interventional

The purpose of the proposed study is to evaluate the effectiveness of a cognitive behavioral therapy (CBT) and yoga program for improving posttraumatic stress disorder (PTSD) symptoms and sleep quality in people who have experienced a traumatic event and are reporting trauma symptoms.

NCT ID: NCT02366403 Completed - Clinical trials for Stress Disorders, Post-Traumatic

Breathing Meditation Intervention for Post Traumatic Stress Disorder

Start date: October 14, 2015
Phase: N/A
Study type: Interventional

Post traumatic stress disorder (PTSD) is a condition that develops as a result of exposure to a traumatic event. The purpose of this study is to determine whether a breathing meditation technique (Sudarshan Kriya Yoga; SKY) provides a treatment benefit that is as effective as the standard intervention. Patients' PTSD symptoms will be monitored before treatment, at the end of treatment, one month after treatment and 12 months after treatment.

NCT ID: NCT02362477 Completed - Clinical trials for Posttraumatic Stress Disorder

Telemental Health and Cognitive Processing Therapy for Female Veterans With Military-related PTSD

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

The immediate objective of this project is to evaluate the clinical effectiveness of a telemental health modality (video-teleconferencing) for providing an evidence-based group intervention to female rural veterans, Reservists, National Guardsmen, and civilians suffering with PTSD. This study is an expansion, seeking to add a treatment arm of women, to an already CDMRP-funded study that completed in July 2014 treating male combat veterans with military-related PTSD. The long-term objective of this project is to disseminate an empirically sound TMH PTSD protocol for male and female veterans, Reserve and Guard that will extend the use of CPT to remote rural sites. It is hypothesized that using VTC, will be as effective as the in-person mode of service delivery for providing CPT.

NCT ID: NCT02357680 Completed - Depression Clinical Trials

Diaries for Critically Ill Patients Written by Relatives

Start date: March 15, 2015
Phase: N/A
Study type: Interventional

This study will investigate the effect of diaries written by relatives for critically ill patients on the risk of posttraumatic stress symptoms. Utilizing a randomized controlled design pairs of one patient and one relative will be assigned to either diary intervention or standard care. The effect of the diary will be evaluated using a questionnaire 3 months post charge. The results of this study will add to the body of knowledge on how diaries may help critical care survivors and their relatives to proceed with their lives.

NCT ID: NCT02356861 Withdrawn - Clinical trials for Traumatic Brain Injury (TBI)

LED Light Therapy to Improve Cognitive & Psychosocial Function in TBI-PTSD Veterans

Start date: March 1, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to learn if an experimental treatment can help thinking ability, and memory in Veterans with mild or moderate traumatic brain injury (mTBI), and post-traumatic stress disorder (PTSD). The experimental treatment is called transcranial, light-emitting diode (LEDs) therapy,and uses groups of LEDs mounted inside a helmet. The helmet is worn on the head, and the LEDs shine painless light on the sides, middle and front of the head through the scalp. The participants receive a series of LED treatments which take place as outpatient visits at the VA Boston Healthcare System, Jamaica Plain Campus. The LEDs contain near-infrared diodes. The FDA considers the LED device used here, to be a non-significant risk device. The LEDs do not produce heat.

NCT ID: NCT02336971 Completed - PTSD Clinical Trials

Individual PE vs Couples' CBT for Combat-Related Posttraumatic Stress Disorder

Start date: November 2011
Phase: Phase 3
Study type: Interventional

This study seeks to enroll 76 couples in which one of the members is a combat-veteran with PTSD. Each couple will be randomized into one of two cognitive-behavioral therapies developed specifically as a treatment for PTSD—either Prolonged Exposure (PE) [1-4] or Cognitive-Behavioral Couples Therapy (CBCT) [5-7]. Whereas, PE was developed as a one-on-one therapy that focuses on treating the individual, CBCT for PTSD incorporates the partners into therapy and seeks to directly address relationship functioning while treating the PTSD symptomatology. Both partners in each couple will complete a battery of several assessments measuring various aspects of psychological distress (e.g., depression, PTSD) and relationship functioning at five time-points throughout the study. But, only the partners assigned to the CBCT group will be involved in the actual therapy sessions. Analysis will be carried out to identify whether any significant differences exist between PE and CBCT in treating PTSD and improving relationship functioning.

NCT ID: NCT02336568 Not yet recruiting - PTSD Clinical Trials

The Effect of 21-Days Intranasal Oxytocin on Patients With Post Traumatic Stress Disorder (PTSD)

Start date: March 2015
Phase: Phase 4
Study type: Interventional

Oxytocin (OT) - a neurohormone and neuromodulator which is mainly synthesized in the hypothalamus - is a mediator stress regulation and improves social bonding. Recently, several theoretical studies suggested that PTSD patients have abnormal functioning of the OT system. According to these theories, dysfunction in the oxytocin system may modulate the interpersonal impairment that characterizes PTSD, and therefore intranasal OT may potentially relieve these symptoms. In two current studies that were conducted in Rambam health care we found that a single dose of intranasal OT reduces anxiety and irritability symptoms, and enhances emotional empathy and compassion, in patients with PTSD. The main goal of this study is to examine the effects of 21-days intranasal Oxytocin on clinical symptoms and social function in these patients.