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Depressive Disorder clinical trials

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NCT ID: NCT03285139 Completed - Clinical trials for Postpartum Depression

Peer Administered CBT for PPD

PL-CBT
Start date: January 3, 2018
Phase: N/A
Study type: Interventional

Postpartum depression (PPD) affects up to 20% of women and has profound effects on mothers and their infants. Unfortunately, fewer than 15% of women with PPD receive evidence-based care. This is at least partly due to significant difficulties faced by women in accessing cognitive behavioural therapy (CBT), a preferred 1st line treatment. In Ontario at present, there is a significant lack of personnel trained to deliver CBT. This study will utilize a randomized controlled trial design (with wait list controls) and recruit 70 participants to determine if women with a past history of PPD (i.e., lay peers) can be trained to deliver effective group CBT to women with current PPD. If peers can be trained to provide effective CBT, more women would receive treatment and the burden of PPD on women, families, and the healthcare system would be significantly reduced.

NCT ID: NCT03283670 Completed - Clinical trials for Depressive Disorder, Major

Inhaled Nitrous Oxide for Treatment-Resistant Depression: Optimizing Dosing Strategies

NARSAD
Start date: November 22, 2016
Phase: Phase 2
Study type: Interventional

The purpose of the study aims to determine whether different concentrations of nitrous oxide (N2O) have different antidepressant effects for adults with treatment-resistant major depression.

NCT ID: NCT03283254 Completed - Clinical trials for Postpartum Depression (PPD)

PREPP: Preventing Postpartum Depression

PREPP
Start date: February 12, 2018
Phase: N/A
Study type: Interventional

The primary aim of this study is to determine if a behavioral intervention targeting maternal caregiving of young infants can increase infant sleep and reduce fuss/cry behavior, and thereby (1) reduce the incidence and/or severity of postpartum maternal depression and (2) improve the quality of the mother-infant interaction and subsequent child development. Specifically, the study team will investigate: (1) the effectiveness of the intervention compared to usual care; (2) if the effects of the intervention can be detected in the assessments of the quality of mother-infant interaction; (3) if there are prenatal and/or postnatal biomarkers that can help identify infants whose behavior is more likely to play a role in their mothers' depression; (4) if these markers differentiate which infants will be most responsive to the intervention(s); and (5), if assessments of brain function at birth and at 4-6 weeks of age provide biological nodal points for identifying the effects of the intervention on infant brain development. Participants will be recruited during their 2nd trimester, and will be randomly separated into one of two groups: a group that receives coaching in parenting techniques (4 in-person coaching sessions and 1 phone session) or one that receives treatment as usual.

NCT ID: NCT03282448 Completed - Clinical trials for Peripartum Depression

Video-based Family Therapy for Peripartum Depression in Home Visited Mothers

Start date: May 26, 2017
Phase: N/A
Study type: Interventional

This pilot study will explore the feasibility and acceptability of implementing a family-based treatment, using HIPAA-compliant video-based communication technology, for adolescents (pregnant and post-delivery) with peripartum depressive symptoms within the context of home visiting.

NCT ID: NCT03279913 Completed - Depression Clinical Trials

NEUROFEEDSTIM : Therapeutic Use of Neurofeedback in Depression in Association With TMS

NEUROFEEDSTIM
Start date: December 18, 2017
Phase: N/A
Study type: Interventional

Neurofeedback is an increasingly researched technique for the treatment of many psychological disorders, such as attention deficit / hyperactivity disorder (AD / HD), depression, or substance abuse. This technique would allow patients to regulate their cortical electroencephalographic activity while receiving a visual or auditory feedback on the cortical electroencephalographic activity. Changes in the electroencephalogram (EEG) would thus be correlated with changes in cortical activity and thus with symptoms. On the electroencephalographic plane, the depression appears associated with relatively more alpha activity (in "resting state", 8-13 Hz) in left than in right frontal cortex. This difference in alpha activity between frontal regions is known as alpha asymmetry in depression. As a reminder, increased alpha activity indicates a decrease in cortical activation. This alpha asymmetry appears to be associated with a decrease in sensitivity to reward. It is on these bases that the modification of the alpha asymmetry has become one of the most frequent objectives of the studies on the use of neurofeedback in depression. Transcranial magnetic stimulation (TMS) also offers a non-invasive and painless method of effective cerebral stimulation in psychiatric disorders and especially depression. It received a favorable opinion from the Food & Drug Administration (FDA) in the United States for the treatment of this pathology. This treatment is still under evaluation in France. The results are promising but improvements must be done to increase its effectiveness. TMS offers stimulation of brain tissue in a localized and non-invasive manner. The principle consists of a brief electric current passing through a coil which generates a transient magnetic field inducing an electric field through conductive fabrics. TMS modifies neuronal activity in target superficial brain structures, but also modulates neuronal circuit activity. In recent years, the concept of "state dependency TMS" has been developed. It suggests that the activation state of neuronal circuits before and after stimulation alters the effect of stimulation. Thus, the efficacy of TMS could be amplified in depression by taking into account the cerebral activity during the stimulation sessions, in particular on the electroencephalographic plane. However, TMS may also help patients increase their EEG response during Neurofeedback sessions. The combination of stimulation techniques and brain-machine interfaces such as neurofeedback is still little studied at present. A study on the combined use of TMS and Neurofeedback by EEG in depression would therefore be an innovative approach and in line with the latest data from the literature. Design : Prospective, monocentric, non-randomized, non-comparative, unblinded study.

NCT ID: NCT03277846 Completed - Depression Clinical Trials

The Safety and Efficacy of Nexalin Trans-cranial Electrical Stimulation Stimulation for the Treatment of Depression

TES
Start date: September 1, 2017
Phase: N/A
Study type: Interventional

The purpose of this research study is to determine whether Nexalin Trans-Cranial Electrical Stimulation (TES) is an effective treatment for depression among patients who are candidates for ECT. A secondary aim to assess whether Nexalin can be used as an alternative to ECT. Although Nexalin has been approved for use in the US, using Nexalin to treat depression in this way is investigational and experimental. If Nexalin is found to be an alternative to ECT, it could offer a safer treatment for depression with less side-effects and a lower cost. !!! NOTE !!! Post Script / Post Study. The ECT arm (profiling subjects as ECT accepters vs. rejecters) was dropped owing to site objections by referring clinicians. Accordingly, the study was framed as a simple comparison between TES and SHAM TES.

NCT ID: NCT03275961 Completed - Depression Clinical Trials

Stress Management and Resiliency Training (SMART) Integrated Into Treatment of Major Depression

Start date: November 29, 2016
Phase: N/A
Study type: Interventional

The investigators are doing this research study to find out if the Stress Management and Resiliency Training (SMART) therapy will help subjects with their major depression treatment.

NCT ID: NCT03275766 Completed - Clinical trials for Major Depressive Disorder

Transcranial Magnetic Stimulation (TMS) for Motor Symptoms in Psychiatric Disorders

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

Psychomotor slowing may occur in major psychiatric disorders, such as major depressive disorders or schizophrenia spectrum disorders. It refers to slowing of fine motor skills, motor planning and gross motor behavior. In major depression and schizophrenia, psychomotor slowing is associated with alterations of premotor cortex, dorsolateral prefrontal cortex and basal ganglia. This randomized, sham-controlled, prospective trial will test, whether 15 sessions of repetitive transcranial magnetic stimulation (rTMS) may ameliorate psychomotor slowing in schizophrenia or major depression.

NCT ID: NCT03272516 Completed - Depression, Anxiety Clinical Trials

Mindfulness Based Cognitive Therapy (MBCT) for Primary Care Patients

Start date: September 12, 2017
Phase: N/A
Study type: Interventional

This study is done to evaluate the effects of Mindfulness Based Cognitive Therapy (MBCT) for primary care patients that have mild to moderate symptoms of depression and anxiety. Half of the study participants will receive treatment as usual (TAU), and the other half will receive TAU plus MBCT. The investigators will be comparing changes in symptoms of depression and anxiety between the groups, and hypothesize that the TAU plus MBCT group will have significantly lower symptoms of depression and anxiety compared to TAU group post-intervention

NCT ID: NCT03268434 Completed - Unipolar Depression Clinical Trials

Evaluation of Metacognitive Training for Depression (D-MCT) in Outpatient Care

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

Aim of the current study is to investigate the acceptance and efficacy of Metacognitive Training for Depression (D-MCT) compared to cognitive remediation in outpatients with major depressive disorders in a randomized, controlled, assessor-blind, group trial.