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Depressive Disorder clinical trials

View clinical trials related to Depressive Disorder.

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NCT ID: NCT05286645 Recruiting - Depressive Disorder Clinical Trials

Intervention Effect of High Definition Transcranial Direct Current Stimulation (HD-tDCS) on Depressive Disorder

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

To investigate the intervention effect of high definition transcranial direct current stimulation (HD-tDCS) on suicidal ideation and somatic symptoms in patients with depressive disorder and its underlying neural mechanism by MRI.

NCT ID: NCT05285215 Recruiting - Clinical trials for Depression, Postpartum

Integrated Psychological Program for Management of Postnatal Depression and Persistent Postpartum Pain After Childbirth

CODEPAD-II
Start date: April 18, 2022
Phase: N/A
Study type: Interventional

The integrated psychological program (IPP) is based on evidence from the local population showing that the interventional components (mindfulness training, music listening, video counselling) are amenable to implementation in the outpatient care setting. Incorporating innovative digital mobile and electronic applications in the care of an increasingly technology-savvy population will be strategic. The proposal will transform the healthcare model for treating postnatal depression (PND) and persistent postpartum pain (PPP).

NCT ID: NCT05280015 Recruiting - Depression Clinical Trials

Microbiotherapy in Characterized Depressive Disorder

PROMOOD
Start date: June 8, 2022
Phase: Phase 2
Study type: Interventional

The study aims to evaluate the contribution of a multi-targeted microbiotherapy at 12 weeks in depressed-patients in a situation of failure of a 1st line of antidepressant treatment and treated in add-on with a 2nd antidepressant, venlafaxine.

NCT ID: NCT05275413 Recruiting - Quality of Life Clinical Trials

mHealth Intervention to Reduce Maternal Postnatal Depression and Promote Family Health

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

The proposed study is to test the effectiveness of a culturally-attuned, family-based mobile health (mHealth) intervention in reducing symptoms of postnatal depression and promoting health among expectant mothers in Hong Kong. Using a family perspective, the proposed mHealth intervention will engage family members, including expectant fathers and grandparents, in providing support to expectant mothers. Expectant mothers and their family members will be recruited at antenatal clinics at two public hospitals in Hong Kong and randomized to receive the family-based mHealth intervention (experimental), the mother-only mHealth intervention (experimental), or the health education (control). Maternal depression, anxiety and stress, perceived social support, health-related quality of life, and perceived family cohesion will be assessed at recruitment and four weeks after childbirth. For family members, symptoms of anxiety and stress, health-related quality of life, and perceived family cohesion will be measured.

NCT ID: NCT05274620 Recruiting - Depression Clinical Trials

Integrating a Suite of Mental Health Apps for Depression in a Healthcare Setting

Start date: May 1, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the implementation of IntelliCare as a frontline intervention within health care settings.

NCT ID: NCT05273996 Recruiting - Clinical trials for Major Depressive Disorder

Predictors of Cognitive Outcomes in Geriatric Depression

NBOLD
Start date: September 28, 2021
Phase: Phase 4
Study type: Interventional

This study will focus on examining effects of stress on long-term mood and cognitive outcomes of late-life depression. It will also example the neural underpinnings of these changes using structural and functional brain imaging. Understanding how effects of stress in older depressed adults, as well as factors that might minimize those effects, lead to particular mood and cognitive outcomes will inform future development of novel prevention strategies.

NCT ID: NCT05269732 Recruiting - Clinical trials for Postpartum Depression

CBT for Postpartum Depression and Infant Emotion Regulation

Start date: June 17, 2022
Phase: N/A
Study type: Interventional

The primary objective of this study is to determine if online group cognitive behavioral therapy (CBT) for maternal postpartum depression (PPD) added to treatment as usual (TAU) leads to greater improvements in infant emotion regulation (ER) than maternal receipt of TAU alone immediately post-treatment and 6 months later. This study will also aim to determine what mechanisms PPD treatment leads to changes in infant ER.

NCT ID: NCT05267340 Recruiting - Depression Moderate Clinical Trials

Neural Mechanisms of Meditation Training in Healthy and Depressed Adolescents: An MRI Connectome Study PART 2

Start date: February 8, 2023
Phase: N/A
Study type: Interventional

The primary objective will be to study changes in putamen connectivity and depression severity in depressed teens with meditation training. H1: Putamen node strength will increase in the training group compared to the active controls. H2: This increase in node strength will correlate with practice amount recorded by participants. H3: There will be a significant reduction in self-rated depression symptoms following the training as measured by the Reynolds Adolescent Depression Scale (RADS-2), compared to controls. H4: This reduction will correlate with the increase in putamen node strength. Design and Outcomes: The current research study design will utilize an individually randomized group treatment, open-label, active-controlled clinical trial to test the efficacy and safety of the investigator's innovative mindfulness meditation intervention (Training for Awareness Resilience and Action [TARA]) on the primary outcome (Putamen structural node strength) and secondary outcome (depression symptoms measured using Reynolds Adolescent Depression Scale [RADS-2]) in depressed adolescents between the ages of 14 to 18 years old.

NCT ID: NCT05266443 Recruiting - Clinical trials for Irritable Bowel Syndrome With Subthreshold Depression

Lactobacillus-containing Cultured Milk Drink Alleviates Depression Score Among Adults With Irritable Bowel Syndrome

Start date: November 22, 2019
Phase: N/A
Study type: Interventional

Irritable bowel syndrome (IBS) is frequently associated with any form of psychiatric comorbidities including subthreshold or subclinical depression. Modification of gut ecology with probiotics has implicitly improved IBS and depressive symptoms. However, the efficacy of probiotics on IBS with existing subthreshold depression remain elusive. Therefore, the aim of this study is to evaluate the effects of lactobacillus-containing cultured milk drink on depression scores in adults diagnosed with IBS.

NCT ID: NCT05259943 Recruiting - Clinical trials for Major Depressive Disorder

Microdosing Psychedelics to Improve Mood

Start date: July 15, 2023
Phase: Phase 2
Study type: Interventional

This trial aims to examine the safety and efficacy of small (2mg) sub-hallucinogenic doses of psilocybin in people with Major Depressive Disorder.