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PTSD clinical trials

View clinical trials related to PTSD.

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NCT ID: NCT02572830 Completed - PTSD Clinical Trials

Reconsolidation and EMDR

Start date: December 31, 2015
Phase: N/A
Study type: Interventional

Blocking of reconsolidation by pharmacological or behavioral means offers the therapeutic possibility of weakening traumatic memories in posttraumatic stress disorder (PTSD). Two reconsolidation-based interventions, propranolol and extinction learning, have been shown to weaken fear memories in human healthy subjects. However, the success of these interventions seems to be limited to weak conditioned fear memories. This calls for new, potentially more efficacious, interventions to be tested. Bilateral eye movements seem to be a promising candidate intervention for blocking reconsolidation due to the compelling evidence of Eye Movement Desensitization and Reprocessing as effective treatment in PTSD. The investigators' aim is to test bilateral eye movements as an active reconsolidation-blocking intervention in an optimized differential fear conditioning procedure that the investigators have recently developed. This novel experimental assay creates stronger fear memories in healthy individuals.

NCT ID: NCT02523664 Completed - PTSD Clinical Trials

Neural Correlates of Stress Hormones

Cort-fMRI
Start date: January 2014
Phase: N/A
Study type: Interventional

To investigate which neuronal correlates underlie cortisol-induced enhancement of memory retrieval in PTSD and BPD.

NCT ID: NCT02504931 Completed - Clinical trials for Alcohol Use Disorder

Serotonin Selective Reuptake Inhibitor Treatment of Dual Diagnosis Post-traumatic Stress Disorder and Alcohol Problems

DDx
Start date: April 2011
Phase: Phase 4
Study type: Interventional

The investigators propose to conduct a clinical trial to evaluate sertraline treatment efficacy in a large sample of military veterans with a dual diagnosis of PTSD and Alcohol Use Disorder who are receiving Cognitive and Behavioral Therapy as part of the VA-system's new dual diagnosis program. The study is designed as an efficacy trial of sertraline used as an adjunct to Cognitive Behavioral Therapy (CBT) in the treatment of PTSD/Alcohol dual diagnosis. There are two outcomes of interest, namely PTSD symptom improvement and also decreased alcohol consumption. The investigators are interested to know whether or not sertraline is superior to placebo in improving the symptoms of either one or both of these two disorders. Even though sertraline is a treatment of choice for PTSD, the investigators expect that the comorbid condition of alcohol dependence will complicate the treatment of PTSD and that the clustered subgroups will show differential treatment response with sertraline. The primary objective of the present study is to identify subgroups of alcohol dependent persons with PTSD who will either benefit or not benefit from treatment with SSRI's. The proposed study will enroll veterans with PTSD and dually-diagnosed alcohol dependence in a 12-week treatment providing sertraline vs. placebo medication as an adjunct to manualized CBT and will specifically test the hypothesis that subtypes of alcohol dependence can be used to predict which patients respond well and which subgroup responds poorly to SSRI treatment.

NCT ID: NCT02499432 Completed - PTSD Clinical Trials

Improving Implementation of Evidence Based PTSD Psychotherapy for Veterans in the Community

Start date: January 2013
Phase: N/A
Study type: Interventional

To further increase the access of evidence based psychotherapies for Veterans with Posttraumatic Stress Disorder, we propose to offer training and intensive consultation to community-based providers in Cognitive Processing Therapy for Posttraumatic Stress Disorder. However, we believe that many clinicians may not implement Cognitive Processing Therapy or take advantage of consultation after initial training. For this reason, we propose to examine the effectiveness of an enhanced training method, which would add Motivational Interviewing to the standard Cognitive Processing Therapy training. Motivational Interviewing is a form of collaborative discussion for strengthening motivation and commitment to change. We hypothesize that augmenting the standard Cognitive Processing Therapy training with these techniques will reduce providers' reluctance to fully implement the interventions.

NCT ID: NCT02499029 Completed - PTSD Clinical Trials

N-acetylcysteine in the Treatment of PTSD and Addiction

NAC
Start date: February 2013
Phase: Phase 2
Study type: Interventional

Examine the effects of N-acetylcysteine on PTSD symptoms, craving and substance use in veterans with PTSD and comorbid substance use disorders.

NCT ID: NCT02492334 Completed - Clinical trials for Alcohol Use Disorder

Doxazosin for PTSD and Alcohol Use Disorder

Start date: July 2016
Phase: Phase 2
Study type: Interventional

The study will test the efficacy of doxazosin, a long-acting and selective alpha-1 adrenergic antagonist, as compared to placebo in reducing PTSD symptomatology and alcohol use severity.

NCT ID: NCT02486692 Completed - PTSD Clinical Trials

Pilot Evaluation of AboutFace: Novel Peer Education Resource for Veterans

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

The purpose of this study is to evaluate the AboutFace peer education website for the purpose of reducing stigma and improving attitudes toward seeking mental health services among Veterans.

NCT ID: NCT02457780 Completed - PTSD Clinical Trials

Stress Management Program for World Trade Center (WTC) Responders

Start date: August 2013
Phase: N/A
Study type: Interventional

Many responders to the World Trade Center (WTC) disaster continue to experience significant mental and physical health problems. Two of the most common health problems, post-traumatic stress disorder (PTSD) symptoms and respiratory illness, often occur together. Mental health conditions, such as PTSD, make physical illnesses worse and interfere with treatment. The primary goal of this study is to test a mind-body treatment designed to reduce both PTSD and respiratory symptoms.

NCT ID: NCT02453347 Completed - Depression Clinical Trials

Cranial Electrotherapy Stimulation (CES) Therapy

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

The primary aim of this proposed study is to gather preliminary data for CES use in treating PTSD and anxiety symptoms in OEF/OIF Veterans with PTSD and a history of TBI.

NCT ID: NCT02447744 Completed - Depression Clinical Trials

Neural Changes Associated With a Mindfulness-based Intervention for Young Adults With Childhood Maltreatment

Start date: August 1, 2014
Phase: N/A
Study type: Interventional

Childhood trauma is remarkably prevalent, and it has long lasting impact on mental health and neural development. This trial aims to see whether the 8-week mindfulness based intervention can reduce stress related psychological symptoms for young adults with childhood maltreatment, and whether it can promote neural plasticity.