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Establishing growth cohort of children with attention deficit hyperactivity disorder

Establishing growth cohort of children with attention deficit hyperactivity disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096794
Enrollment
Unknown
Registered
2025-02-06
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Growth monitoring and influencing factors of children with attention deficit hyperactivity disorder

Interventions

ADHD (Review Section):None
ADHD (Forward-Looking Part):None
Case group:None

Sponsors

Sichuan Provincial Maternity and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1.Subjects meet the diagnostic criteria of ADHD: American Handbook of Diagnosis and Statistics of Mental Disorders; 2.When diagnosed with ADHD, the physiological age was 6-12 years old; 3.Wechsler intelligence test >=80; 4.ADHD was diagnosed before the trial, and no drug or systematic non-drug intervention was received before the diagnosis. After the diagnosis of ADHD, drug or behavioral therapy may or may not be accepted; 5.Provide informed consent signed and dated by the subject and/or his/her guardian.

Exclusion criteria

Exclusion criteria: 1.Organic diseases of nervous system, mental retardation, schizophrenia, mental retardation, generalized developmental disorder and other primary mental disorders (such as conduct, anxiety, emotional disorders, etc.); 2.Those who have used central excitatory drugs (including ADHD drugs) and other chronic diseases that need long-term medication before being diagnosed with ADHD; 3.Accurate height measurement (such as severe scoliosis, meningocele, or severe bone deformity) cannot be obtained; 4.Patients with complete epiphysis closure; 5.Unable to provide complete medical records or expected to be unable to fully follow up or collect complete medical records; 6. Other conditions that the investigator considers unsuitable for inclusion in this study.

Design outcomes

Primary

MeasureTime frame
Height standard difference points;

Secondary

MeasureTime frame
weight;Questionnaire scoring;

Countries

China

Contacts

Public ContactLi Wei

Sichuan Provincial Maternity and Child Health Care Hospital

1257430445@qq.com+86 28 65978601

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026