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Mental Health clinical trials

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NCT ID: NCT01678846 Completed - Mental Health Clinical Trials

Good Schools Study

GSS
Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether use of the Good Schools Toolkit is effective in reducing violence against children in primary schools.

NCT ID: NCT01622244 Completed - Mental Health Clinical Trials

Coordinated Access to Care From Hospital Emergency Departments

CATCH-ED
Start date: November 2012
Phase: N/A
Study type: Interventional

The study will assess the effectiveness and cost-effectiveness of providing brief, intensive case management for frequent users of hospital Emergency Departments who have mental health and/or addictions problems. The goals of the intervention are to support patients' transition to community-based health and social services and supports - including primary and urgent psychiatric care, peer support and other community services and supports - so as to improve patient wellbeing and reduce avoidable ED visits and hospitalizations.

NCT ID: NCT01462058 Completed - Mental Health Clinical Trials

The Role of Vitamin D Supplementation on Well Being and Symptoms of Depression During the Winter Season in Health Service Staff

D3-vit-SAD
Start date: October 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate whether vitamin D3 (70 micrograms) is better than placebo in preventing depression symptoms among employees in health care

NCT ID: NCT01427231 Completed - Mental Health Clinical Trials

Short-term Effect of Glucose and Sacharose Ingestion on Cognitive Performance and Mood in Elderly

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

The objective of the current study is to determine the acute effect of a glucose drink and a sacharose drink compared to a placebo on cognitive performance in elderly with light memory complaints. The investigators expect that the sugar containing drinks will improve memory and attentional functions. Furthermore, blood glucose response will be measured.

NCT ID: NCT01155687 Completed - Stress Clinical Trials

Psychosocial Counseling in Afghanistan

Start date: September 2009
Phase: N/A
Study type: Observational

The assessment intends to investigate the efficacy of psychosocial counseling for the treatment of help seeking individuals with psychosocial problems in Mazar-e-Sharif, Afghanistan. Treatment was administered by local counselors who had received specific education and training

NCT ID: NCT01083225 Completed - Mental Health Clinical Trials

Effect of Patient Participation in Mental Health Care

Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of individual user involvement in an outpatient mental health center. The intervention consists of patients completing a self-report symptom and problem questionnaire and reviewing it with a clinician.

NCT ID: NCT01057368 Completed - Mental Health Clinical Trials

The Effects of Well-being Interventions on Affect, Attention, Sleep, Social Stress and Pain Regulation

Start date: November 2009
Phase: N/A
Study type: Interventional

This study is focused on the brain mechanisms and peripheral biological correlates of two different forms of meditation--mindfulness-based and compassion/loving-kindness. Project 1 is focused on the impact of compassion/loving-kindness meditation on emotional reactivity and emotion regulation. Project 2 is focused on the neural and behavioral correlates of mindfulness meditation and attention and pain regulation. In addition, Project 2 will examine the relations between changes in oscillatory rhythms during meditation and attention and pain processing. Project 3 will examine the impact of meditation on spontaneous brain activity during sleep. This project will also examine the impact of intensive meditation on regional changes in slow wave activity during subsequent sleep. Each of these projects will be conducted on the same participants so that interrelations among the various measures collected in the different projects can be examined. We believe that this study will dramatically advance the understanding of the mechanisms by which meditation produces changes in behavioral and biological processes.

NCT ID: NCT01037946 Completed - Quality of Life Clinical Trials

Family to Family: Psychoeducation to Improve Children's Outcomes in HIV+ Families

Start date: September 2005
Phase: N/A
Study type: Interventional

This project aims to support adults in HIV-affected families in order to improve their well-being. UCLA's Center for Community Health (CCH), in collaboration with the Thai Ministry of Public Health, Bureau of Epidemiology, will implement the Family-to-Family (F2F) intervention in order to improve the social, behavioral and mental health outcomes for families affected by HIV. In Phase 1, the investigators pilot tested the current intervention contents and activities by collecting qualitative data from HIV+ families in the four district hospitals in Chiang Rai and Nakohn Ratchasima provinces selected for the proposed study. The findings from Phase was used to develop intervention content, as well as the format and style of the intervention for Phase 2. In addition, the findings from Phase 1 was used to finalize the assessment measures the investigators will use in Phase 2. In Phase 2, 410 families with HIV+ parents from 4 district hospitals in Chiang Rai & Nakhon Ratchasima Provinces will be recruited to an intervention to benefit their school-aged children aged 6-17 years. At their clinical care site,the investigators randomly assigned families to either: 1) F2F, a psychoeducational intervention for HIV+ parents and family caregivers; or 2) a Standard Care condition. The impact of the F2F intervention will be monitored over 24 months.

NCT ID: NCT00988390 Completed - HIV Infections Clinical Trials

Mothers Living With HIV and Their Adolescent Children

TALK LA
Start date: February 2005
Phase: N/A
Study type: Interventional

- Context: Mothers living with HIV (MLH) and their children face predictable challenges: maintaining physical and mental health, parenting while ill, and addressing HIV-related stressors. - Objective: To evaluate the efficacy of a family-based intervention over time; to contrast the life adjustments of HIV-affected families and their non-HIV-affected neighbors in the current treatment era. - Design: Randomized controlled trial of MLH and a longitudinal comparison of MLH to a neighborhood cohort using random effect regression. - Participants and Intervention: MLH (n = 339) and their school-age children (n = 259) were randomly assigned to receive 1) an intervention of 16 sessions in a cognitive-behavioral, small-group format; or 2) control. MLH and their children were compared to non-HIV-affected families recruited at shopping markets. Participant retention was high: 84% at 6 months, 83% at 12 months, and 78% at 18 months. - Main Outcome Measures: Family functioning and conflict, mental and physical health, sexual behavior, and substance use.

NCT ID: NCT00922922 Completed - Mental Health Clinical Trials

Duration and Direct Cost of Behavioral Health Concerns in Pediatric Primary Care

EI
Start date: April 3, 2009
Phase:
Study type: Observational

The purpose of this study is to compare the duration and direct cost of pediatric primary care visits consisting of medical concerns only, behavioral concerns only, and medical and behavioral concerns.