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Depression clinical trials

View clinical trials related to Depression.

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NCT ID: NCT06449807 Recruiting - Mental Health Clinical Trials

Effects of Crossover Point Exercise on Depression, Anxiety and Stress in Chinese Postmenopausal Women

Start date: February 20, 2024
Phase: N/A
Study type: Interventional

To analyze the effects of the Crossover Point (COP) Exercise Program on Chinese postmenopausal women.

NCT ID: NCT06447909 Recruiting - Depression Clinical Trials

Randomized Controlled Trial of a Behavioral Training App

Start date: March 27, 2024
Phase: N/A
Study type: Interventional

The investigators propose addressing and evaluating the efficacy of a behavioral, contingency management app by conducting a randomized controlled trial (RCT) that will evaluate the app compared to a placebo app control group. Participants will be randomly assigned to immediate intervention using the treatment condition or to a placebo app condition. Participants will not know which condition they are assigned to until after the study completion; they will also not know that they are using the treatment app until after the study completion. The sample will consist of 100 families of school-age children (ages 6-12) who display significant behavioral problems. The treatment app is a task management platform containing a self-directed rewards system through which caregivers can assign token rewards to their children for completing routine tasks (e.g., cleaning their room, completing homework). Participants in the placebo app condition will have a similar user experience, however, tokens are assigned non-contingently (dispensed daily, rather than based on task completion). While participants will not be required to complete any tasks or behaviors in the app as part of their participation in the study, they will be asked to use the app at least once per day for 8 weeks. Given the self-directed nature of the treatment app (parents decide how frequently they access the app-based rewards system and how many tasks they assign to their child), parent involvement in the intervention will vary slightly in duration. However, based on the literature and routine practice, we anticipate parents will log in at least once a day to assign tasks to their child and follow up on completed rewards. Assessments (see details below) will occur at baseline, weekly during the intervention, and at the end of the study. The study will take about 8 weeks in total to complete once participants have been enrolled in the app.

NCT ID: NCT06447428 Recruiting - Clinical trials for Late Life Depression

One-Year Trajectory of Cognitive Changes in Patients With Late-life Depression in the Short Term

Start date: June 1, 2023
Phase:
Study type: Observational

The purpose of this study was to investigate the one-year trajectory of cognitive change in elderly patients with depression, to explore the transfer characteristics and transfer rules of various states of cognitive impairment in patients, to predict the relevant risk factors of cognitive decline, and to find possible influencing factors affecting state change, so as to provide a theoretical basis and reference for subsequent targeted intervention research on geriatric depression.

NCT ID: NCT06446856 Recruiting - Schizophrenia Clinical Trials

EVEN - Effects of VR on Empathy for Nature in Patients With Psychosis and Depressive Disorders

EVEN
Start date: May 27, 2024
Phase:
Study type: Observational

Study group: Experimental study to evaluate empathy, compassion, and nature connectedness before and after an immersive virtual reality experience in patients with depressive disorder, patients with psychotic disorder and healthy control subjects (subjects between 18 and 65 years of age). Primary hypothesis: The increase in nature connectedness explored by virtual body ownership of a tree in VR differs depending on the health condition (schizophrenia, depression, healthy controls).

NCT ID: NCT06444581 Recruiting - Depressive Symptoms Clinical Trials

Effectiveness of the Universal Prevention Program Super Skills for Life in Schools

Start date: January 8, 2024
Phase: N/A
Study type: Interventional

This study aims to evaluate the effectiveness of a 12-session cognitive-behavioral transdiagnostic protocol for Spanish children aged 8 to 12 within an educational context, Super Skills for Life. The program, designed to enhance emotional management and social interaction skills, will be delivered in a group format and supplemented with multimedia materials. The study will compare outcomes between an intervention group and a wait-list control group.

NCT ID: NCT06440798 Recruiting - Depression Clinical Trials

Mental Health Content and Mental Health Outcomes

Start date: January 1, 2024
Phase:
Study type: Observational

The study will aim to explore the relationship between mental health content on social media and health behavior, addressing a gap in empirical research. Using the Theory of Planned Behavior, a survey with over 600 participants will examine associations between exposure to mental health content and behaviors like help-seeking and self-diagnosis.

NCT ID: NCT06440785 Recruiting - Stress Clinical Trials

Taylor Swift and Mental Health Outcomes

Start date: January 1, 2024
Phase:
Study type: Observational

A study in Singapore will explore the potential of pop culture, particularly Taylor Swift's music, in influencing young adults' attitudes toward mental health. With the highest prevalence of mental illness among this age group, the study will aim to investigate whether engagement with Swift's songs and social media will be associated with attitudes crucial for help-seeking, such as recognizing mental health issues and being open to professional services. Conducting a survey of over 600 young adults, the researchers will assess participants' mental health symptoms, engagement with Swift's content, social media and demographics, mental health help-seeking attitude and mental health self-diagnosing behavior.

NCT ID: NCT06438276 Recruiting - Depression Clinical Trials

Psychiatric Outreach Nurses Supporting Adolescent Mental Health

JAPSY
Start date: May 6, 2024
Phase:
Study type: Observational

The study evaluates the effectiveness and cost-effectiveness of the outreach work of psychiatric registered nurses (RN) and the experiences of professionals in the field. The service is provided in school environment. First, the study will assess the effectiveness of brief interventions provided by psychiatric outreach nurses on the perceived mental health and quality of life of adolescents (12-16 year old pupils) and their use of social and health services, compared to the support/treatment provided by conventional student welfare services at 6 and 12 months follow-up. The intervention is an outreach service provided by psychiatric nurses. In the intervention, the psychiatric registered nurse will implement interventions such as usual care, discussion, psychoeducation, substance abuse skills and various methods (such as interpersonal psychotherapy = IPT-N and Cool Kids) and motivational interviewing. Secondly, an economic evaluation of the service will be carried out at 6 and 12 months follow-up. The economic evaluation will be carried out from the perspective of the Wellbeing Services County, including the costs of implementing the intervention model and its effects on adolescents' use of student welfare services as well as other social and health services. Primarily, the economic evaluation will use quality-weighted life years as a measure of effectiveness. Also analysis using depression, anxiety and substance use measures will be conducted. Thirdly, the study will explore the experiences of psychiatric nurses implementing the service as well as the experiences of their collaborators in schools (public health nurses, school social workers, psychologists, doctors and teachers) about the service and its implementation.

NCT ID: NCT06432959 Recruiting - Depression Clinical Trials

Incorporating Positive Affect Promoting Activities Into Cognitive Behavioral Therapies

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

In this study, the investigators will test whether the incorporation of positive affect promoting activities in treatment sessions improves outcomes in the context of CBT for depression and DBT for problems of emotion dysregulation. In clinics focused on each of these treatments, the investigators will evaluate these treatments with and without the addition of positive affect promoting activities.

NCT ID: NCT06431386 Recruiting - Bipolar Disorder Clinical Trials

Behavioural Activation Therapy and Esketamine for Resistant Depression

Start date: June 2024
Phase: N/A
Study type: Interventional

This is a randomized clinical trial to test the effectiveness of combining a proven psychological intervention called behavioural activation therapy alongside esketamine treatment for treatment resistant major depressive episodes in individuals with major depressive disorder or bipolar disorder. Encouraging participants to practice new behaviours while their mood is improved through esketamine treatment may lead to more lasting recovery from depression.