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Depression clinical trials

View clinical trials related to Depression.

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NCT ID: NCT03153904 Active, not recruiting - Depression Clinical Trials

Connecticut Child STEPs

Start date: October 2013
Phase: N/A
Study type: Interventional

Connecticut Child STEPS is a randomized controlled trail investigating the effectiveness of MATCH-ADTC in treating anxiety, depression, trauma, and/or behavioral problems in children seeking services at four Department of Children and Families (DCF) funded clinics in the state of Connecticut. The study will evaluate child outcomes following two forms of therapist training in the MATCH model.

NCT ID: NCT03123991 Active, not recruiting - Depression Clinical Trials

Applying the Spanish Version of the UP-A as a Universal School-based Anxiety and Depression Prevention Program

Start date: October 10, 2016
Phase: N/A
Study type: Interventional

The current study proposes to extend transdiagnostic treatment research to adolescents by establishing initial pre to post-treatment and follow-up outcomes associated with the use of the Spanish Version of the Unified Protocol for the Treatment of Emotional Disorders in Adolescents (UP-A; Ehrenreich-May, Bilek, Buzzella, Kennedy, Mash, & Bennett, 2016) as a universal school-based preventive intervention.

NCT ID: NCT03122158 Active, not recruiting - Clinical trials for Major Depressive Disorder

Escitalopram in the Treatment of Adolescents With Major Depressive Disorder or Anxiety Disorders

Start date: April 8, 2017
Phase: Phase 4
Study type: Interventional

Escitalopram has been approved by FDA in the treatment of adolescents with major depressive disorder since March 2009. To date, there are only 3 clinical trials assessing the effect and validity of escitalopram on major depressive disorder, which of them has resulted in inconsistent findings. In the present study, the authors aimed to assess the effect and validity of this drug in the treatment of adolescents with major depressive disorder and or anxiety disorders.

NCT ID: NCT03107039 Active, not recruiting - Depressive Symptoms Clinical Trials

Exploring the Effects of Strength Training on Depressive Symptoms and Cardiovascular Risk in Black Men

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

This study will address a gap in the literature and advance the field of minority men's health. Specifically, it will be the first randomized controlled trial of resistance exercise as a dual intervention for depression symptoms and CVD risk reduction with depressed Black men.

NCT ID: NCT03067506 Active, not recruiting - Clinical trials for Major Depressive Disorder

Cognitive and Mood Assessment Data in Major Depressive Disorder Using Digital Wearable Technology

Start date: March 1, 2017
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate feasibility and compliance with a novel method for assessing mood and cognition in participants with major depressive disorder (MDD).

NCT ID: NCT03001440 Active, not recruiting - Clinical trials for Depressive Disorder, Major

A 7-year Assessment on Subject Understanding of ZYBAN/ WELLBUTRIN Associated Risks

Start date: October 2016
Phase: N/A
Study type: Observational

Branded bupropion hydrochloride products including ZYBAN and WELLBUTRIN range are approved for the treatment of smoking cessation and depressive disorders respectively. The Risk Evaluation and Mitigation Strategy (REMS) for ZYBAN was initially approved in 2010 and consists of a Medication Guide and a timetable for REMS assessments submission at 18 months, 3 years and 7 years from the date of initial approval of REMS. The present study is a 7-year REMS assessment to evaluate subjects' understanding of the potential serious risk of neuropsychiatric adverse events associated with the use of ZYBAN, WELLBUTRIN, WELLBUTRIN SR, and WELLBUTRIN XL. The assessment will be a 20-minutes Knowledge, Attitudes and Behavior (KAB) survey and will be conducted among approximately 125 subjects currently using or who have filled a prescription for a branded bupropion product for smoking cessation within the 6 months prior to survey administration. ZYBAN, WELLBUTRIN, WELLBUTRIN SR, and WELLBUTRIN XL are registered trade marks of the GSK group of companies.

NCT ID: NCT02989727 Active, not recruiting - Depression Clinical Trials

Melancholic Symptoms in Bipolar Depression and Responsiveness to Lamotrigine

Start date: November 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if patients with melancholic bipolar II depression are more responsive to lamotrigine than patients with non-melancholic bipolar II depression. To do this, the investigators will re-analyze a previous clinical trial that evaluated lamotrigine as a treatment for bipolar II depression (GSK-SCA100223; NCT00274677).

NCT ID: NCT02986945 Active, not recruiting - Depressive Symptoms Clinical Trials

Community-Partnered Participatory Development of Mobile Interventions

Start date: December 2016
Phase: N/A
Study type: Interventional

The purpose of the study is to test an experimental method, a text-messaging app called B-RESILIENT, for improving participants' mood. B-RESILIENT is a text messaging app adaptation of a Resiliency Course, developed by community members known as Building Resiliency and Community Hope.

NCT ID: NCT02980783 Active, not recruiting - Clinical trials for Cheek Line Depressions

A Study to Evaluate the Effectiveness of Juvéderm® VOLIFT®™ With Lidocaine for Dynamic Radial Cheek Line Skin Depressions

BEAM
Start date: October 2016
Phase: Phase 4
Study type: Interventional

This study will evaluate the effectiveness of Juvéderm® VOLIFT®™ with Lidocaine for dynamic radial cheek line skin depressions.

NCT ID: NCT02972203 Active, not recruiting - Depression Clinical Trials

MINDFUL-PC: Integrating Mindfulness Into the Patient-Centered Medical Home

MINDFUL-PC
Start date: October 2015
Phase: N/A
Study type: Interventional

Specific aims for this pilot study are: (Behavioral health outcomes aim): Among primary care patients, compare the effectiveness of an 8-week mindfulness-based intervention (Mindfulness Training for Primary Care[MTPC]) vs. a 60-minute introduction to mindfulness plus referral to community resources on measures related to anxiety, depression, and stress, and self-management of chronic illness. (Medical Regimen Adherence Aim): Among primary care patients, compare the effectiveness of MTPC vs. 60-minute introduction to mindfulness on the initiation and maintenance of an action plan. (Patient-Provider Relationship Aim): To examine the effects of level of primary care provider mindfulness training on successful referral to program, patient-provider relationship measures, and on patient action plan initiation and maintenance.