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Adolescent Depression clinical trials

View clinical trials related to Adolescent Depression.

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NCT ID: NCT06325605 Completed - Clinical trials for Adolescent Depression

Efficacy and Safety of Bifidobacterium Combined With High-frequency Transcranial Magnetic Stimulation in the Treatment of Adolescent Depression

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

A total of 100 patients with adolescent depression who were admitted to our hospital between March 2022 and October 2022 were selected. On the basis of double blinding, these patients were randomly divided into the observation group(n=50) and the control group(n=50) using a random number table. 5S management method was used in the whole process of treatment to improve the hospital environment, increase the work efficiency and reduce the occurrence of cross infection through the effective implementation of the five steps of sort(Seiri), set in order(Seiton), shine (Seiso), standardize(Seiketsu) and sustain(Shitsuke).

NCT ID: NCT06072677 Recruiting - Clinical trials for Adolescent Depression

Adolescent Mood During Puberty and Testosterone

AMPT
Start date: August 24, 2023
Phase: N/A
Study type: Interventional

Starting at puberty, female adolescents are nearly three-times more likely to develop internalizing disorders, like depression, while male adolescents are two-times more likely to develop externalizing disorders, like attention deficit hyperactivity disorder (ADHD). This divergence between the sexes during puberty suggests sex-specific pathways of risk and differential effects of sex hormones. The purpose of this research is to determine: 1) sex-specific neural and endocrine features of the pubertal transition that may mediate sex differences in adolescent mood disorders, and 2) the neurophysiological basis of susceptibility to hormone change during puberty.

NCT ID: NCT04613453 Recruiting - Clinical trials for Adolescent Depression

Reducing Adolescent Suicide Risk: Safety, Efficacy, and Connectome Phenotypes of Intravenous Ketamine

Start date: January 21, 2022
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if intravenous ketamine reduces suicidal thinking compared to an active placebo (midazolam) in adolescents who have treatment resistant depression and a recent history of a suicide event (defined as a suicide attempt, emergency room evaluation for suicidal thinking, or a transition to inpatient care for suicidality in the past 120 days). The primary objective of this study is to determine whether ketamine reduces suicidal ideation (as measured via the C-SSRS, recent ideation scale) relative to an active control, midazolam, 48-hours after first administration in adolescents with TRD at high suicide risk.

NCT ID: NCT04603053 Completed - Anxiety Disorders Clinical Trials

Determining Effectiveness of an mHealth Intervention to Provide Adolescent CBT

Start date: November 9, 2020
Phase: N/A
Study type: Interventional

Washington University will evaluate the acceptability and effectiveness of a mobile health (mHealth) intervention to provide cognitive behavioral therapy for adolescents with depression.

NCT ID: NCT03154008 Completed - Depression Clinical Trials

Predictors of Response to Treatment for Depression

PORT
Start date: June 1, 2017
Phase: N/A
Study type: Interventional

The current study will examine neurophysiological, specifically event-related potential (ERP), measures of emotional processing as predictors of response to cognitive behavior therapy for adolescent depression.

NCT ID: NCT02017535 Completed - Clinical trials for Adolescent Depression

An Adaptive Treatment Strategy for Adolescent Depression-Continuation

PTAD GIA
Start date: June 2012
Phase: Phase 1/Phase 2
Study type: Interventional

Aim 1: Assess the feasibility and acceptability of the personalized continuation treatment strategy. Aim 2: Estimate variances of primary and secondary outcomes with the continuation treatment. Aim 3: Conduct exploratory hypothesis-generating analyses to inform further development of the personalized continuation treatment strategy to be tested in a subsequent R01 proposal.

NCT ID: NCT01857518 Recruiting - Clinical trials for Adolescent Depression

Depression in Adolescents. A Cerebral Structural, Diffusion, and Functional Magnetic Resonance Imaging Study

ADODEP
Start date: August 31, 2013
Phase: N/A
Study type: Interventional

Adolescence is a critical period for the development of depressive disorders. As adolescence also is a critical period for brain maturation, it may be hypothesized that maturation changes in emotional circuits could underlie vulnerability for depression. The aims of the study are (1) to identify the changes in brain morphometry, white matter microstructure, and functioning, in networks associated with depression features in adolescents, and (2) to assess the effects of treated pathology on brain structure by comparing the neuroimaging measures obtained in adolescents at inclusion with those at follow-up.

NCT ID: NCT01802437 Completed - Clinical trials for Adolescent Depression

An Adaptive Treatment Strategy for Adolescent Depression

PTAD
Start date: November 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is: 1. to find out how long teenagers getting talk therapy (interpersonal psychotherapy) for depression should get therapy before the therapist decides whether or not the teenager is improving enough, and 2. to compare two ways of providing treatment to teenagers who have not improved enough.

NCT ID: NCT01170520 Recruiting - Clinical trials for Adolescent Depression

Repetitive Transcranial Stimulation (rTMS) for Resistant Depression in Adolescents

Start date: August 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The investigators hypothesis that repetitive transcranial Stimulation (rTMS) is a safe and effective add-on therapy for resistent depression in adolescent patients. A group of adolescents suffering from non psychotic major depression that was resistant to at least 2 drug trials and a trail of psychotherapy will be recruited. After an informed consent procedure for both parents and patients, patients will go through a clinical and cognitive evaluation. They will receive a protocol of 4 weeks (20 work days) of rTMS using the figure of 8 magstim coil at 100% threshold, 42 trains of 4 seconds each, intertrain interval of 30 sec to the LDPC, 1680 pulses per day. Then they will be reevaluated.

NCT ID: NCT00399776 Completed - Clinical trials for Adolescent Depression

Bone Mineral Content and Bone Metabolism in Adolescents on Antipsychotic Therapy

Start date: October 2006
Phase: N/A
Study type: Observational

We hypothesize that antipsychotic induced hyperprolactinemia can decrease bone mineral accrual and decrease bone mineral content (BMC) in adolescents on antipsychotic therapy. Specifics Aims 1. To determine if antipsychotic therapy leads to decreased bone mineral accrual and decreased bone mineral content in a group of adolescents on antipsychotic therapy by comparing them to an ethnicity, gender and pubertal stage matched control group. 2. To determine the relationship between serum concentrations of prolactin, sex steroids and bone turnover markers in adolescents on antipsychotic therapy and an ethnicity, gender and pubertal stage matched control group.