Selenium Supplementation for Improving Depression in Children and Adolescents: Efficacy and Mechanistic Study

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age12-18
SponsorFirst Affiliated Hospital of Chongqing Medical University

About this trial

The purpose of this study is to investigate the role and mechanisms of selenium in depression among children and adolescents, aiming to provide new insights for understanding the pathogenesis and treatment of depression in this population.

Eligibility criteria

Qualifiers

Aged 12-18 years;

Diagnosed with major depressive disorder according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), using the K-SADS-PL diagnostic tool;

A score of ≥28 on the Children's Depression Rating Scale-Revised (CDRS-R);

Adequate visual and auditory abilities to complete the study;

Disqualifiers

Patients with severe psychiatric disorders such as bipolar disorder, schizophrenia, bulimia nervosa, anorexia nervosa, or primary obsessive-compulsive disorder;

Those with severe physical illnesses or other life-threatening conditions; patients in a current depressive episode with a clear suicidal plan or history of suicide attempt;

Individuals with a history of substance or drug abuse;

Those requiring immediate hospitalization for psychiatric disorders;

Trial design

Treatments tested in this trial

  • selenium yeast supplementation
  • Placebo yeast supplementation

Treatment groups

172 Participants
are divided into 2 treatment groups