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Depression clinical trials

View clinical trials related to Depression.

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NCT ID: NCT04114565 Completed - Clinical trials for Major Depressive Disorder

Prevalence of Major Depression Among Immigrants in Santiago, Chile

STRING
Start date: July 29, 2019
Phase:
Study type: Observational

The general aim of this study is to explore the prevalence of major depressive disorder and the use of mental health services in the immigrant populations in the Metropolitan Region of Santiago, Chile. The hypotheses are: 1. A healthy immigrant effect will be observed in the studied population by which their prevalence of major depressive disorder will be lower than the prevalence in the general Chilean population. 2. A significant association will be observed between the loss of socio-economic position after migration and a greater probability of major depressive disorder. 3. A significant association will be observed between the report of victimization experience(s) in the previous year and a greater probability of major depressive disorder. 4. A significant association will be observed between financial difficulties and a greater probability of major depressive disorder. The sampling framework of the Chilean National Institute of Statistics (INE) from the 2016 Census will be used for the purpose of this research. The sampling units are as follows: 1. Primary sampling units (PSUs): conglomerates or groups of adjoining houses, organized in spatial blocks (200 households on average) 2. Secondary sampling units (SSUs): individual households within each of the conglomerates selected in the first stage 3. Final sampling units: persons meeting the study's inclusion criteria Multi-stage random probability sampling involving a 3-stage sampling design will be used - first, the sampling of the primary sampling units (PSUs); second, the sampling of households within the selected PSUs and finally, the random sampling of a household member. Participants (n=1,100) will then take part in a 45-minute interview. This interview will be a household survey using the modular version of the Composite International Diagnostic Interview (WHO-CIDI) looking at exploring a broad spectrum of factors traditionally associated with increased risk of affective disorders: 1. Sociodemographics 2. Finance 3. Variation in socioeconomic position 4. Experience of victimization 5. Discrimination 6. Experience of childhood adversity

NCT ID: NCT04111887 Completed - Depressive Symptoms Clinical Trials

Pilot Study Comparing Two Versions of Group Cognitive-behavioral Indicated Prevention Programs

Start date: October 10, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effectiveness of two depression prevention programs and a control brochure for college students. Participants may experience reductions in depressive symptoms and prevention of future depression.

NCT ID: NCT04109196 Completed - Depression Clinical Trials

Examining Changes in Microbiota Over the Course of PTSD Treatment

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

The overall goals of this project are to evaluate the use of 5-day intensively-delivered Cognitive Processing Therapy to treat PTSD and to determine the associations between the microbiome, salivary cytokines, and the presence of and recovery from PTSD. Specifically, this study is designed to 1) determine whether individual Cognitive Processing Therapy (CPT) delivered twice per day over 5 consecutive days (CPT-5) is tolerable, acceptable, and effective in reducing PTSD symptoms, 2) determine the microbial signatures associated with PTSD, 3) evaluate whether the abundance and composition of microbiota and salivary cytokine levels change over the course of PTSD treatment, and 4) examine whether changes in microbial signatures are associated with changes in cytokine levels.

NCT ID: NCT04109014 Completed - Depression Clinical Trials

FASTLANE II: Reducing Sex, Drug, and Mental Health Risk

FLII
Start date: May 3, 2021
Phase: N/A
Study type: Interventional

The study uses a repeated measures, single group pretest-posttest design methodology to examine the feasibility, acceptability, and preliminary effectiveness of the FASTLANE II intervention aimed at decreasing risky sex behaviors among active methamphetamine using women. The study's methodology consists of two phases: 1) The feasibility and evaluation of recruitment capability and intervention effectiveness, and 2) qualitative acceptability interviews.

NCT ID: NCT04108429 Completed - Depression Clinical Trials

IntelliCare in College Students - Implementation (ICCS-I)

Start date: February 5, 2020
Phase: N/A
Study type: Interventional

This study is a hybrid effectiveness-implementation trial of the smartphone student stress-management app IntelliCare for college students. This intervention will be tested with University of Illinois at Chicago (UIC) and Northern Illinois University (NIU) students. During the study, participants will complete measures of depressive and anxious symptoms, as well as measures of mental health literacy, within the app.

NCT ID: NCT04108234 Completed - Depression Clinical Trials

A Study of HR071603(Ketamine Nasal Spray) in Healthy Subjects

Start date: October 24, 2019
Phase: Phase 1
Study type: Interventional

The study is being conducted to evaluate the safety and pharmacokinetics of HR071603 in healthy subjects.

NCT ID: NCT04107025 Completed - Depression Clinical Trials

Effects of a Legal Support Program on Women Experiencing Domestic Violence

Start date: April 28, 2017
Phase: N/A
Study type: Interventional

Intimate partner violence (IPV) is a major public health concern. Worldwide, 1 in 3 women have experienced domestic abuse/ violence in their lifetime. In most cases, family lawyers, advocates are first contact before the police. If the children are involved, finding the legal options become the priority for women before leaving the abuser. The purpose of this study was to compare the effectiveness of the HELP (Health, Education Legal Support Program) intervention among IPV survivors.

NCT ID: NCT04106388 Completed - Depression Clinical Trials

Virtual Behavioral Health Integration

VBHI
Start date: August 14, 2019
Phase: N/A
Study type: Interventional

The primary objective is to evaluate the effectiveness of the virtual behavioral health integration (VBHI) program compared to usual care, on reducing the total cost of care reimbursed from Medicare and value-based contracts within 90 days of a patient's primary care visit.

NCT ID: NCT04106375 Completed - Clinical trials for Recurrent Major Depression

Neural Effects of Wellness Classes in Women With Vulnerability to Depression ("The Women's Wellness Study")

WWS
Start date: March 5, 2016
Phase: N/A
Study type: Interventional

The primary objective of the study is to examine the efficacy of mindfulness based cognitive therapy (MBCT) on the prevention of relapse in women with a history of depression. Additionally, the investigators will explore how brain activity might be affected in several brain regions as a result of MBCT. This study consists of two groups, a patient group consisting of women with a history of depression and a control group consisting of healthy women. All participants within the patient group will receive an 8-week MBCT intervention program and will continue their normal medication treatment. Participants will undergo, both pre and post intervention, various behavioral and neuroimaging tasks to assess intervention effects of well-established psychological measurements related to cognitive and emotional function.

NCT ID: NCT04105790 Completed - Depressive Symptoms Clinical Trials

The Acceptability and Effectiveness of Stepped Care Psychoeducation Classes in Rural Manitoba

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

This study will examine the acceptability and effectiveness of using a stepped care treatment model, and specifically, the CBTm classes, in a rural population. The introduction of CBTm classes, developed in Winnipeg and used in outpatient mental health clinics there, is new to Adult Community Mental Health in the Prairie Mountain Health region. This research is being done to explore whether this is a treatment model that is effective at reducing symptoms of anxiety and depression and also whether it affects the workload for Community Mental Health Workers in a more rural area. Further, this research is being done to explore whether clients perceive this form of services to be useful and acceptable.