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Development and Preliminary Validation of a Mental Health Intervention Program for Caregivers of Children and Adolescents with Mood Disorders

Development and Preliminary Validation of a Mental Health Intervention Program for Caregivers of Children and Adolescents with Mood Disorders

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123504
Enrollment
Unknown
Registered
2026-04-27
Start date
2026-04-30
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Mood Disorder

Interventions

experimental group:the mental health intervention program developed in this study
control group:routine psychological care and health education

Sponsors

Affiliated Hospital of Guangdong Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. The child or adolescent (aged =18 years) under their care has been diagnosed with a mood disorder (including depressive disorder, bipolar disorder, etc.) by the attending physician according to international diagnostic criteria such as ICD-10 or DSM-5; 2. The caregiver is a direct relative of the patient, or is recognized as the primary guardian, and has been involved in caregiving for =5 days per week for a duration of =3 months; 3. The caregiver possesses adequate reading comprehension skills and is capable of effective communication; 4. Voluntary participation in this study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. The caregiver has a physician-diagnosed history of severe mental disorders (e.g., schizophrenia, cognitive impairment, etc.) or has severe communication difficulties that preclude completion of the study assessments; 2. The caregiver is expected to miss more than two sessions of the intervention program during the study period; 3. Other conditions that the investigators deem unsuitable for participation in this study; 4. Failure to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
anxiety;depression;

Countries

China

Contacts

Public ContactYu Yangyang

Affiliated Hospital of Guangdong Medical University

1015204383@qq.com+86 150 1443 4264

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026