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Resilience, Psychological clinical trials

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NCT ID: NCT03673098 Completed - Clinical trials for Resilience, Psychological

The BRIgHT Program: Building Resilience in HIV Together

Start date: November 5, 2018
Phase: N/A
Study type: Interventional

This is the second phase of a two-part study. In the first phase (Protocol ID: R34AT009170), the investigators refined and piloted the Relaxation Response Resiliency (3RP) intervention for women age 50 and over who are living with HIV, a group especially burdened by stressors related both to aging and to living with chronic disease. In this part of the study, the investigators will use data from the first phase to further adapt the intervention manual, and test the final product via a small randomized controlled trial in the same population.

NCT ID: NCT03458936 Recruiting - Depression Clinical Trials

Resilience in Adolescent Development

RAD
Start date: December 2016
Phase:
Study type: Observational [Patient Registry]

The RAD study is a longitudinal study to prospectively characterize the biological mechanisms of resilience in adolescents and young adults at risk for developing depression. The study will capture biomarkers from the domains of socio-demographic and clinical data, cognitive and psychological assessments, fluid-based biomarkers, neuroimaging and EEG. Such biomarkers will compose a human biosignature of resilience and identify risk factors for depression, contributing to effective treatment selection or may represent moderators of response or non-response to treatments in subjects with depression. A cohort of 1,500 participants, age 10-24 will be recruited over a 5 year period. Participants will be followed for 10 years following an initial baseline visit. Study visits are conducted 4 times per year.

NCT ID: NCT03328598 Terminated - Bereavement Clinical Trials

A Community-based Resilience Program of Only-child Loss Parents

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

This is a community-based participatory research aiming at helping the only-child loss parents to be happier and resilient from bereavement. It is a psycho-behavioral intervention research. There are two intervention programs in this study. One is derived from a foreign psychotherapy, developed by an American psychologist and has been testified the effectiveness in promoting happiness. Another one is developed by the researchers based on the previous cross-sectional survey and interviews with those bereaved parents. The researchers will apply randomized controlled trial to testify and compare those two intervention programs in a Chinese community.

NCT ID: NCT03308981 Completed - Clinical trials for Resilience, Psychological

Efficacy of the REThink Therapeutic Online Game

Start date: September 15, 2016
Phase: N/A
Study type: Interventional

This study aims to test the efficacy of the REThink therapeutic online video game. Children and adolescents (N = 150), aged between 10-16 years, will be randomly assigned to one of three groups: 1) REThink group, 2) Rational-Emotive-Behavioral Education (REBE) group and 3) wait-list condition.

NCT ID: NCT03270943 Completed - Adolescent Behavior Clinical Trials

The S.M.A.R.T. Project: Stress Management and Resilience Training for Teens

Start date: September 5, 2017
Phase: N/A
Study type: Interventional

The rate of depression increases markedly over the course of adolescence. Adolescents struggling with depression are often set on a maladaptive behavior trajectory which may lead to academic challenges, substance abuse, risky sexual behavior, impairment in relationship building, and suicidality. The S.M.A.R.T Project (Stress Management and Resilience Training for Teens) is designed to learn about mood in teens, and whether emotional well-being can be improved with an 8 week class. The study proposes to refine and test the feasibility of a mindfulness-based self-compassion training program for adolescents who are experiencing subsyndromal depression, comparing it with a "healthy lifestyles" group program as a comparison attention-control for the treatment intervention. Secondarily, the study will explore the impact of these programs on measures of psychopathology and well-being (i.e. depressive symptoms and resilience).

NCT ID: NCT03071887 Completed - Clinical trials for Resilience, Psychological

Resilience Intervention for Older, HIV-Infected Women

BRIgHT
Start date: November 27, 2017
Phase: N/A
Study type: Interventional

The goal of this study is to refine and pilot the Relaxation Response Resiliency (3RP) intervention for women age 50 and over who are living with HIV, a group especially burdened by stressors related both to aging and living with chronic disease. The investigators will adapt the 3RP resiliency intervention to the needs of this population and conduct preliminary testing of the group intervention via an open pilot study.

NCT ID: NCT02908932 Completed - Cognition Clinical Trials

Ranger Resilience and Improved Performance on Phospholipid Bound Omega-3's

RRIPP-3
Start date: August 2016
Phase: N/A
Study type: Interventional

The goal of this study is to determine if supplementation with krill oil concentrate containing the phospholipid-bound omega-3 fatty acids improves performance on specific cognitive tests that underlie key elements in U.S. Army Infantry Basic Officer Leaders Course (IBOLC) and in Ranger School (Training) at Fort Benning, Georgia (GA).

NCT ID: NCT02603133 Completed - Clinical trials for Burnout, Professional

Web-based Implementation for the Science of Enhancing Resilience Study

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

Resilience means a healthcare provider's ability to cope, recover, and learn from stressful events, as well as their access to resources that promote health and well-being. Neonatal intensive care unit (NICU) health professionals' need to have particularly good resilience, because their work is extremely stressful and their patients, fragile preterm infants, require their undivided attention. The investigators propose a feasible and engaging intervention to enhance resilience among NICU health professionals promoting their ability to provide safe care.

NCT ID: NCT01828983 Completed - Family Members Clinical Trials

Telephone Support During Overseas Deployment for Military Spouses

Start date: April 2011
Phase: N/A
Study type: Interventional

Deployment impacts both service member and family, and the cost can be high. Spouses' reactions to deployment may include emotional distress, loneliness, anticipatory fear or grief, somatic complaints, and depression. The goal is to help spouses learn ways to manage stress and solve problems related to deployment and reintegration, communication, managing long distance relationships, and other common problems. The study will compare telephone support groups to online education sessions. The study will enroll 160 spouses. In the Telephone Support groups, a group leader and participants will meet 12 times over six months to focus on education, skills building and support. Education Only online sessions will provide the same education content, without skills building or support. Content includes strategies to reduce or eliminate communication difficulties during deployment, how to find help; practical concerns during deployment; fostering resilience and decreasing stress; fostering relationships while apart, negotiating roles and relationships; changes during deployment; strategies to support the spouse and the service member; and cues to alert spouses when to seek mental health services for the family or themselves. Outcomes will include resilience, depression, anxiety and coping behaviors. Telephone data collection will be conducted at baseline, six and twelve months.