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Stress Disorders, Traumatic clinical trials

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NCT ID: NCT03113175 Completed - Clinical trials for Post Traumatic Stress Disorder

Collabri Flex - Effect of Collaborative Care for People With Anxiety Disorders in General Practice

Start date: January 15, 2018
Phase: N/A
Study type: Interventional

The aim of the study Collabri Flex is to: - Develop a Danish model for collaborative care for patients with anxiety in general practice, based on past experience gained in the Collabri Project. - Examine the impact of this model compared with liaison-consultation for people with anxiety in a randomized controlled design from selected endpoints.

NCT ID: NCT03110302 Completed - Clinical trials for Posttraumatic Stress Disorder

In-Home Exposure Therapy for Veterans With Post Traumatic Stress Disorder (PTSD)

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

This study examines clinical and process outcomes following variable length prolonged exposure (PE) for posttraumatic stress disorder (PTSD) delivered by one of three treatment modalities: home-based telehealth (HBT), office-based telehealth (OBT), or in-home-in-person (IHIP).

NCT ID: NCT03103165 Completed - Depression Clinical Trials

SimCoach Evaluation: : A Virtual Human Intervention to Encourage Servicemember Help-seeking for PTSD and Depression

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

SimCoach, a computer program featuring a virtual human that speaks and gestures in a videogame-like interface, is designed to encourage servicemembers to seek help to improve their psychological health.

NCT ID: NCT03088384 Completed - Clinical trials for Stress Disorders, Post-Traumatic

Ketamine Infusion Therapy for PTSD in Combat Veterans

Start date: November 28, 2016
Phase:
Study type: Observational

Klarisana is conducting an observational study in San Antonio, Texas to see if there are tangible improvements in the symptoms of post traumatic stress disorder (PTSD) in combat veterans after receiving a series of six low-dose outpatient infusions of ketamine.

NCT ID: NCT03077919 Completed - Clinical trials for PostTraumatic Stress Disorder

Effectiveness and Acceptability of Stellate Ganglion Block for Posttraumatic Stress Disorder Symptoms - Effectiveness

Start date: May 25, 2016
Phase: N/A
Study type: Interventional

This is a multisite, randomized, blinded, sham-procedure-controlled study to evaluate the efficacy of right-sided stellate ganglion block (SGB) on the acute symptomatology of Post traumatic Stress Disorder (PTSD), evaluated by the Clinician-Administered PTSD Scale (CAPS-5) clinical interview at pre-treatment and at 8 weeks. This entry describes the effectiveness study.The acceptability study is described in a separate entry.

NCT ID: NCT03056157 Completed - Clinical trials for Post-traumatic Stress Disorder

Psychosocial Rehabilitation After Moral Injury and Loss With Adaptive Disclosure

Start date: March 1, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to determine the efficacy of Adaptive Disclosure for Moral Injury and Loss (AD-MIL), a combat-specific psychotherapy for war-related PTSD stemming from Moral Injury (MI) and traumatic loss (TL) with Iraq and Afghanistan War Veterans with PTSD. AD-MIL will be compared to Present Centered Therapy (PCT). AD-MIL is a modified version of Adaptive Disclosure (AD), which has been modified and extended to solely treat MI and TL by targeting psychological and behavioral obstacles to occupational, relationship, and family functioning, as well as quality of life. PCT is a manualized evidenced-based PTSD treatment used in several large-scale PTSD trials. The primary end-point is psychosocial functioning (improvements in social, educational and occupational functions and improvements in quality of life). Secondary end-points include PTSD, depression, and shame and guilt. The investigators will also explore the impact of AD-MIL on anger and aggressive behaviors, suicidal ideation, and alcohol abuse.

NCT ID: NCT03048929 Completed - Clinical trials for Posttraumatic Stress Disorder

Inflammation and Threat Sensitivity in PTSD

K01
Start date: April 1, 2019
Phase: Early Phase 1
Study type: Interventional

The overall goals of this study are to examine the relationship between chronic inflammation and threat and reward sensitivity, and to determine the effects of acute inflammation on threat sensitivity, in individuals with and without moderate to severe PTSD symptoms. The investigators will first conduct an observational study to examine the relationship between chronic inflammation and neural and behavioral measures of threat sensitivity. Then, the investigators will conduct a randomized, double-blind, placebo-controlled, between-subjects study to examine the effects of acute inflammation on neural and behavioral measures of threat sensitivity.

NCT ID: NCT03045016 Completed - Clinical trials for Acute Stress Disorder

Efficacy of Prazosin in Preventing Post-traumatic Stress Disorder

PRAZOSTRESS
Start date: April 21, 2017
Phase: Phase 2
Study type: Interventional

After a traumatic event such as an accident or an assault, victims may experience intense stress symptoms that may evolve into "post-traumatic stress disorder" (PTSD). It is a frequent and serious pathology, which can be complicated by depression, addiction or suicide. Few means are available to prevent PTSD in people who have just undergone trauma. Prazosin is an antihypertensive drug that blocks α1 adrenaline receptors which could help to stop the vicious circle of stress and prevent the development of the disease. The objective of this study is to demonstrate the efficacy of prazosin to prevent PTSD in patients who visit an emergency department after trauma.

NCT ID: NCT03039231 Completed - Clinical trials for Stress Disorders, Post-Traumatic

Investigation of the Freespira Breathing System in the Treatment of Post Traumatic Stress Disorder (PTSD)

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

This study will test the efficacy of the Freespira Breathing System in adults with post traumatic stress disorder (PTSD).

NCT ID: NCT03033069 Completed - Clinical trials for Stress Disorders, Post-Traumatic

A Study of Flexible Dose Brexpiprazole as Monotherapy or Combination Therapy in the Treatment of Adults With Post-traumatic Stress Disorder (PTSD)

Start date: January 26, 2017
Phase: Phase 2
Study type: Interventional

To evaluate the safety, efficacy and tolerability of brexpiprazole (with placebo) as monotherapy or combination therapy with Zoloft (sertraline) in adults with PTSD.