Actively Recruiting

Phase 1
Phase 2
Age: 13Years - 18Years
All Genders
NCT05814640

Sequenced Treatment Alternatives to Relieve Adolescent Depression (STAR-AD)

Led by First Affiliated Hospital of Chongqing Medical University · Updated on 2026-01-27

520

Participants Needed

1

Research Sites

227 weeks

Total Duration

On this page

Sponsors

F

First Affiliated Hospital of Chongqing Medical University

Lead Sponsor

T

The Second Affiliated Hospital of Chongqing Medical University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This project aims to investigate the effectiveness of existing common antidepressants and to provide new evidence for depressed children and adolescents who are not responding to their first treatment.

CONDITIONS

Official Title

Sequenced Treatment Alternatives to Relieve Adolescent Depression (STAR-AD)

Who Can Participate

Age: 13Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 13 to 18 years
  • Diagnosed with major depressive disorder (MDD) with non-psychotic symptoms according to DSM-V
  • Score of 40 or higher on the Children's Depression Rating Scale (CDRS-R)
  • Participants with suicidal thoughts can join if outpatient treatment is safe
  • Sufficient audio-visual ability to participate in the study
  • Written informed consent from the participant and at least one parent
Not Eligible

You will not qualify if you...

  • History of bipolar disorder, schizophrenia, autism, eating disorders, primary obsessive compulsive disorder, pervasive developmental disorder, or unspecified psychosis
  • Serious physical illnesses
  • Substance abuse or dependence
  • Current depression with clear suicidal plans or behavior
  • Need for inpatient psychiatric treatment
  • Severe mental disorders requiring intensive care
  • Two or more failed antidepressant trials lasting at least 8 weeks each with full dose for the last 4 weeks
  • History of intolerance or lack of effect from at least one treatment option in the study
  • Taking medicines that interfere with study treatments
  • Use of antidepressants within 5 half-lives prior to study
  • Received modified electroconvulsive therapy within the past 12 months
  • Pregnant females

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The First Affiliated Hospital of Chongqing Medical University

Chongqing, Province, China, 400000

Actively Recruiting

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Research Team

X

Xinyu Zhou

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

8

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