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Depressive Symptoms clinical trials

View clinical trials related to Depressive Symptoms.

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NCT ID: NCT02656641 Completed - Depressive Symptoms Clinical Trials

Using the PHQ-9 and GAD-7 as Feedback Instruments in Brief Psychotherapy

Start date: November 2015
Phase: N/A
Study type: Interventional

This study will assess the effects of client feedback, using the Patient Health Questionnaire - 9 and Generalized Anxiety Disorder 7-Item Scale, on depression and anxiety in individuals undergoing brief psychotherapy. Client feedback allows therapists to monitor treatment progress in real time. Identifying an easily accessible treatment intervention, which utilizes commonly used scales, that potentially enhances the effect of brief psychotherapy and improves treatment outcomes is a valuable endeavor with clear implications for therapy practices. It is hypothesized that clients who complete these scales each session will show greater symptom improvement than clients who do not complete the scales.

NCT ID: NCT02630758 Completed - Depression Clinical Trials

Mindfulness-Based Yoga Intervention for Women With Depression

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

The purpose of this study was to examine the efficacy of a 12-week mindfulness-based yoga intervention on depressive symptoms and rumination among depressed women.

NCT ID: NCT02474862 Completed - Pregnancy Clinical Trials

Healthy Expectations - A Program for Pregnant Women Experiencing Depressive Symptoms

HE
Start date: March 24, 2015
Phase: N/A
Study type: Interventional

This study is a randomized control trial (RCT) evaluating a Prenatal Walking Program (PWP) in comparison to a Postpartum Prep Program (PPP) comparison group for pregnant women experiencing depressive symptoms. In addition to assessing changes in depressive symptoms, the investigators will examine other key maternal outcomes (maternal functioning, pain, anxiety, stress, fatigue), as well as infant outcomes including birth record data (gestation, weight, Apgar scores, etc) and careful, in-person assessment of infant neurobiological functioning at 30 days postpartum.

NCT ID: NCT02472470 Completed - Depressive Symptoms Clinical Trials

Efficacy and Biological Targets of Response to rTMS Therapy in Youth Depression

Start date: June 2015
Phase: N/A
Study type: Interventional

Youth depression is a debilitating disorder that exacts enormous social, economic and personal cost. Unfortunately, treatments which are conventionally used to treat adult depression have often modest to no efficacy in youth and have side effects. Thus, there is a tremendous imperative to develop new treatments for youth depression. Investigators propose to examine the efficacy of a short form of repetitive transcranial magnetic stimulation (rTMS) for youth depression and examine its biological targets. This will be the first study examining the efficacy of a short rTMS protocol in youth diagnosed with depression who fail responding to or are intolerable to antidepressants. If the results are positive, investigators will have identified a novel treatment that may be both more efficacious, better tolerated and more acceptable treatment for youth depression. Finally, identifying the biological mechanisms leading to treatment efficacy will lead to more personalized treatments for youth depression and will be groundbreaking vis à vis understanding the mechanisms involved in this illness.

NCT ID: NCT02458690 Completed - Stroke Clinical Trials

eIMPACT Trial: Modernized Collaborative Care to Reduce the Excess CVD Risk of Older Depressed Patients

Start date: July 2015
Phase: Phase 2
Study type: Interventional

The objective of this randomized controlled trial is to evaluate whether the investigators modernized IMPACT intervention for depression (eIMPACT), delivered before the onset of cardiovascular disease (CVD), reduces the risk of future CVD. Participants will be primary care patients who are depressed but do not have a history of CVD. Half of the participants will receive standard depression treatment in primary care (usual care), and the other half will receive one year of eIMPACT, a collaborative stepped care program including antidepressants and computerized and telephonic cognitive-behavioral therapy. To evaluate change in CVD risk, the investigators will measure artery function using ultrasound before and after the 1-year treatment period. It is hypothesized that patients who receive the eIMPACT intervention will have greater improvements in artery function than patients who receive usual care.

NCT ID: NCT02410109 Completed - Depressive Symptoms Clinical Trials

Developing an Integrated Model for Home Visitation

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

Perinatal depression is a significant concern, particularly for low-income women. Many cases of perinatal depression are complicated by comorbidities such as post-traumatic stress disorder symptoms, anxiety, and intimate partner violence. Providing perinatal mental health services to women in home visiting programs could have considerable public health significance. This study will develop and test an integrated model of mental health services embedded within home visitation (HV) programs. This model will (1) incorporate a protocol for systematic screening and referral; (2) strengthen formal linkages between HV programs and other components of service systems; (3) promote the capacity of service systems to provide evidence-based early intervention and treatment for depression; and (4) facilitate the receipt of early intervention and treatment services for perinatal depression and comorbid conditions. This will be the first model to our knowledge that systematically integrates screening, referral, and early intervention and treatment for perinatal depression and associated comorbidities within HV programs. The specific aims are: 1. To develop an integrated model of perinatal depression care within HV programs. This integrated model ("SCRIPT") will incorporate screening, referral, and individualized prevention and treatment services. 2. To assess the feasibility of implementing the SCRIPT model with high fidelity in two HV programs. One HV program—DRUM Healthy Families—will use paraprofessionals as interventionists while the other program—M&I Nursing—will use nurses and social workers as interventionists. 3. To determine the impact of the SCRIPT model on depressive symptoms and major depressive episodes.

NCT ID: NCT02358525 Completed - Heart Failure Clinical Trials

Effects of a Rehabilitation Program on Immune Activation and Mood in Heart Failure Patients

Start date: January 2015
Phase: N/A
Study type: Observational

The aim of this descriptive study is to examine potential changes regarding inflammatory cytokine levels, depressive symptoms and quality of life over the course of the 4-week inpatient rehabilitation program which includes a cassette of modalities including counseling, psychosocial education and supervised exercise training as a main pillar, and to further investigate if there are correlations between changes in immune regulation, depressive symptoms and quality of life.

NCT ID: NCT02314390 Completed - Depressive Symptoms Clinical Trials

Group- Versus Individual-Mindfulness-Based Cognitive Therapy: a Randomized Trial

G/I-MBCT
Start date: September 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether both group and individual mindfulness-based cognitive therapy (MBCT) are effective in reducing depressive symptoms in patients with a chronic somatic disease.

NCT ID: NCT02210312 Completed - Depressive Symptoms Clinical Trials

Study of Depressive Symptoms Predicting Postoperative Cognitive Dysfunction

DeprPOCD
Start date: May 2014
Phase:
Study type: Observational

Postoperative cognitive dysfunction (POCD) describes a condition where cognitive functions such as attention, perception, concentration, learning, abstract thinking and problem solving are impaired postoperatively. These changes can be resolved after weeks and months. In some cases, changes are permanent.

NCT ID: NCT02190968 Completed - Depressive Symptoms Clinical Trials

Reducing Residual Depressive Symptoms With Web-based Mindful Mood Balance

Start date: March 2015
Phase: N/A
Study type: Interventional

Many patients report residual depressive symptoms despite seemingly successful treatment. With the investigators' previous funding, we developed - Mindful Mood Balance - an online treatment that targets RDS by teaching specific emotion regulation and depression self-management skills that are entirely compatible with antidepressant treatment. The investigators now propose a controlled study to determine whether MMB is more effective than usual care at reducing RDS and other key outcomes. If successful, MMB's online delivery format would provide high fidelity and low-cost empirically supported management of residual symptoms, leading to more robust remission, improved functioning and sustained recovery from MDD over time.