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Depression clinical trials

View clinical trials related to Depression.

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NCT ID: NCT04655924 Completed - Depression Clinical Trials

Artificial Intelligence in Depression - Medication Enhancement

AID-ME
Start date: June 16, 2022
Phase: N/A
Study type: Interventional

This study will determine the safety and potential effectiveness of a digital health platform aimed at improving treatment outcomes for patients with depression by assisting physicians with clinical decision making about depression treatment.

NCT ID: NCT04652089 Completed - Depression Clinical Trials

7-day Simvastatin and Emotional Processing

SSTEP-HV
Start date: December 3, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

Work in our group has revealed that short-term (7-day) administration of antidepressants produces positive biases in the processing of emotional information in healthy volunteers. Such effect might be an important neuropsychological mechanism of antidepressant action. The current study will investigate the effect of seven-day administration of simvastatin 20mg on emotional and reward processing tasks in healthy volunteers. There is evidence that statins may exert antidepressant effects via anti-inflammatory and anti-oxidant pathways, and it is therefore predicted that simvastatin will have positive effects on emotional and reward processing.

NCT ID: NCT04647318 Completed - Depression Clinical Trials

Physiological Response to Self-compassion Versus Relaxation

Start date: September 24, 2018
Phase: N/A
Study type: Interventional

Compassion-focused imagery (CFI, in which one imagines receiving or giving compassion) can be an effective emotion-regulation technique but some individuals respond as if it is a threat. However, these findings have been based on tasks involving receiving compassion from others. This study sought to examine whether CFI involving self-compassion is less threatening than relaxation and whether any threat-responses decrease with practice. This study will compare the effects of CFI, relaxation and a control task and will explore their effects on self-report symptoms and physiology. It is hypothesized that CFI involving self-compassion is less threatening than relaxation and that any threat-responses decrease with practice.

NCT ID: NCT04647019 Completed - Depression Clinical Trials

The Effects of Wild Blueberries on Depressive Symptoms in Young Adults

BluMood
Start date: November 26, 2021
Phase: N/A
Study type: Interventional

This study aims to investigate the effects of a 6-week dietary intervention of 22 g freeze-dried whole wild blueberry powder. The outcomes include measures of depression, anxiety, anhedonia, cognitive function, and biomarkers of inflammation and oxidative stress.

NCT ID: NCT04646681 Completed - Depression Clinical Trials

Development of a Targeted Patient Portal Intervention to Improve Depression Treatment Adherence and Outcomes

Patient Portal
Start date: March 31, 2021
Phase: N/A
Study type: Interventional

The purpose of this research study is to learn how best to use patient portals to help improve the treatment of mood disorders.

NCT ID: NCT04646369 Completed - Depression Clinical Trials

Screening Wizard- Phase 2

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

Screening Wizard (SW). Primary Care Providers (PCPs) are often uncertain about how to best refer adolescents who screen positive for depression or suicidality. Screen-positive youth who are either not in treatment, or express dissatisfaction with current treatment will be consented by an on-site research assistant (RA). Participants will answer questions via adaptive screens developed in a previous NIMH study (MH100155) for suicidal risk, anxiety, and mania. These will address perceived barriers and preferences about treatment. Participants are then randomized into 1 of 3 groups: 1) Providing the symptoms scores report of results to their provider based on their Screening Wizard responses (Screening as Usual); 2) Providing the symptoms scores report and their responses to treatment preferences and barriers including treatment recommendations their provider might suggest (Screening Wizard 2.0); or 3) Providing the report with treatment recommendations to their provider and a website called SOVA or Supporting Our Valued Adolescent, that is aimed at addressing perceptions about mental health providing support to teens through peer interaction that social workers and doctors moderate on a 24 hour a day basis (Screening Wizard 2.0 + SOVA).

NCT ID: NCT04643964 Completed - Depressive Symptoms Clinical Trials

Brief Video Interventions for Depression

Start date: November 17, 2020
Phase: N/A
Study type: Interventional

In this study, we test brief video interventions for those with elevated depressive symptoms. We randomize participants to one of three conditions. (1) An entrée condition involving in-depth coverage a set of cognitive behavioral therapy (CBT) skills. (2) A sampler condition which introduces three sets of CBT skills. (3) A control condition involving no skills. Among those in the entrée condition, participants are further randomized to one of three CBT skills. We plan on two sets of primary comparisons. First, we will compare the effects of each form of video intervention (i.e., entrée and sampler) to the control condition. Second, we will compare the entrée and sampler conditions. We will recruit participants from Amazon's Mechanical Turk program (MTurk). In the intervention conditions, participants will be asked to watch several videos and practice skills using worksheets. They will also be asked to practice skills introduced in the videos in the week following the intervention. In the control condition, participants will not watch videos. One week after the intervention, all participants will respond to a follow-up assessment.

NCT ID: NCT04640090 Completed - Depression Clinical Trials

Wellness Through Mobile Health

Start date: August 12, 2020
Phase: N/A
Study type: Interventional

This pilot project will evaluate the potential of an affordable smartphone app to improve users' mental well-being.

NCT ID: NCT04639765 Completed - Depressive Symptoms Clinical Trials

Responses to Information on Treatments for Depression

Start date: October 28, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the impact of different messages about depression treatments.

NCT ID: NCT04639557 Completed - Child Development Clinical Trials

Building Regulation in Dual Generations - Telehealth Model

BRIDGE
Start date: September 1, 2020
Phase: N/A
Study type: Interventional

Families who experience maternal mental illness and a variety of chronic stressors are currently underserved by the parenting programs. The investigators propose that impairments in maternal self-regulation, which result in unsupportive parenting, directly impact children's own self-regulation and neurobiology, leading to risk for intergenerational transmission of mental illness. The objective of this study is to develop and evaluate a program that is targeted at improving underlying self-regulatory mechanisms in both mothers with depression and their 3- to 5-year-old children. It is hypothesized that children exposed to maternal mental illness will have greater self-regulatory deficits across emotional and behavioural domains compared to children not exposed to mental illness. The effects of maternal mental illness are expected to be compounded for children of mothers reporting a higher degree of chronic stressors, including poverty, housing instability, violence, and low social support. Further, it is hypothesized that taking a dual-generation intervention approach to addressing self-regulatory mechanisms underlying psychopathology at the level of the mother, child, and dyad (i.e. parenting interactions) will improve both maternal capacities and child outcomes. A feasibility study has been conducted in-person (NCT04347707). Results from this trial showed positive effects on child and mother well-being as well as parenting skills. Our current study will be conducted remotely due to the COVID-19 pandemic to adhere to public health guidelines to reduce in-person contact and physical distance. The objectives for this study are two-fold: 1) establish a better understanding of the self-regulatory processes that are altered in preschool-aged children exposed to maternal mental illness, and determine the mediating role of parenting behaviours, as well as the moderating impact of chronic stress exposure; and 2) evaluate a novel dual-generation intervention for mothers with mental illness using a virtual format and their 3- to 5-year-old children based on existing gold-standard evidence-based approaches.