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Trauma, Psychological clinical trials

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NCT ID: NCT04025463 Completed - HIV/AIDS Clinical Trials

Healing Our Hearts Minds and Bodies: CVD Reduction in Persons With HIV

HHMB
Start date: October 1, 2019
Phase: N/A
Study type: Interventional

"Healing our Minds and Bodies" (HHMB) uses a a hybrid type II effectiveness/implementation study design to increase both patient and organizational readiness to address trauma and CVD risk among African American and Latino persons living with HIV or AIDS (PLWHIV).

NCT ID: NCT03970915 Completed - Hypothermia Clinical Trials

Warm-up Efficiency by Body Warmer Versus Standard Procedure in Severely Traumatized Patients

THERMOTRAUMA
Start date: October 17, 2019
Phase: N/A
Study type: Interventional

Study of adult patients with severe all-cause trauma having a body temperature less than 36°Celsius (C) that is managed by a Mobile Emergency Service team and oriented towards a Vital Emergency Room. Currently two devices are used to warm patients during their care at the scene of an accident: a survival blanket and heating in the emergency vehicle. Despite these two devices many patients arrive in hypothermia (body temperature less than 36°C) in emergency departments. The objective of this study is to evaluate the effectiveness of a body warmer associated with standard warming devices on the correction of hypothermia compared to the standard procedure in severely traumatized patients with hypothermia . It is a national multicentric study with 14 participating Mobile Emergency Service centers and hopefully will include 612 patients. The study will be carried out according to a pattern of 28 successive periods of one week each during the winter period (October to April), for a total duration of 7 months. 14 action periods ON (warming standard procedure + body warmer) and 14 control periods OFF (warming standard procedure) will be run in random order for each center.

NCT ID: NCT03966963 Completed - Clinical trials for Trauma, Psychological

Systematic Case Series Investigating Eye Movement Desensitization Reprocessing (EMDR) Efficacy With Childhood Sexual Abuse Survivors

EMDR
Start date: September 17, 2019
Phase: N/A
Study type: Interventional

This study investigates the effectiveness of EMDR for survivors of childhood sexual abuse. All participants will undertake a standard course of EMDR via the National Heath Service program, alongside a number of questionnaires and a follow-up interview.

NCT ID: NCT03906682 Completed - Depressive Symptoms Clinical Trials

Improving Mental Health and School Performance in Urban Eighth Graders

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

This study assesses: (1) the impact of the Relax, Be Aware, Do a Personal Rating (RAP) Club, a school-based prevention program for urban eighth graders, on students' emotional functioning and education outcomes; (2) potential moderators and mediators of RAP Club's effects; and (3) factors related to the implementation of RAP Club, including cost of delivery and perceptions of key stakeholders.

NCT ID: NCT03826849 Completed - Insomnia Clinical Trials

A Pilot Evaluation of the Insomnia Coach Mobile App

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

This pilot study is designed to test the feasibility, acceptability, and potential effectiveness of a mobile phone application (app) developed by the VA National Center for PTSD (VA NCPTSD) for use by Veterans with insomnia. The primary objective is to assess whether Veterans find the Insomnia Coach app to be satisfactory and feasible to use. Secondary objectives are to determine if use of the app improves subjective sleep quality and sleep parameters (e.g., sleep latency, wake after sleep onset, and total sleep time), as well as other important outcomes (e.g., daily functioning).

NCT ID: NCT03758053 Active, not recruiting - Clinical trials for Alcohol Use Disorder

Adverse Childhood Experiences in Substance-related Disorders

Start date: December 15, 2018
Phase:
Study type: Observational

Aversive childhood experiences (ACE) and their relation to the development of an alcohol use disorder will be measured with fMRI.

NCT ID: NCT03627078 Completed - Clinical trials for Post Traumatic Stress Disorder

Motor Interference Therapy For Traumatic Memories

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

The aim of the study is to compare the effect of motor interference therapy (TIM) to reduce the intensity of discomfort (distress) generated by a traumatic memory compared to a relaxation control maneuver, immediately after the intervention, a week, a month and six months after intervention.

NCT ID: NCT03622138 Completed - Clinical trials for Trauma, Psychological

The Impact Integrated Data System for Quality and Outcomes Tracking of Prevention Programs

Impact
Start date: June 8, 2018
Phase: N/A
Study type: Interventional

There has been substantial progress in developing evidence-based prevention programs (EBPPs) for preventing risky behaviors and promoting positive outcomes for youth. Unfortunately, their adoption, quality implementation, long-term sustainability, and scalability in real world service settings, continues to lag far behind resulting in an inability to achieve the intended broad scale public impact. This SBIR Phase II project will build on the findings and feedback gathered from stakeholders in the Phase I project to fully develop and test the Impact implementation support system. Impact will provide an easy to use, cost- and time-efficient technology platform that is capable of (a) gathering relevant process and outcomes data in a feasible way within real-world service settings; (b) producing real-time analytics (e.g., graphical displays) and meaningful reports at the provider, service setting, and broader levels (e.g., state-wide); and (c) linking data analytics to continuous quality improvement (CQI) feedback to help providers achieve best practices and targeted youth outcomes.

NCT ID: NCT03568591 Completed - Clinical trials for Trauma, Psychological

The Efficacy of a Psychosomatic Intervention

Start date: June 11, 2016
Phase: N/A
Study type: Interventional

This study examines the efficacy of a psychosensory intervention in relation to: Resilience, Type D personality, and physiological effects (on blood pressure, heart rate and salivary cortisol) in a group of people who have self-referred for the trauma resolution psychosensory therapy - Havening Techniques (HT).

NCT ID: NCT03484338 Completed - Depressive Symptoms Clinical Trials

Accelerated Resolution Therapy for Complicated Grief

Start date: February 20, 2018
Phase: N/A
Study type: Interventional

This study will examine whether accelerated resolution therapy (ART) is effective for the treatment of prolonged and complicated grief and associated psychological trauma among older adult hospice caregivers who have experienced the death of an immediate family member at least 12 months ago.