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Clinical efficacy study of mindful self-compassion based group cognitive behavioral therapy for adolescent depression with non-suicidal self-injury

Clinical efficacy study of mindful self-compassion based group cognitive behavioral therapy for adolescent depression with non-suicidal self-injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069751
Enrollment
Unknown
Registered
2023-03-24
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

major depressive disorder

Interventions

Clinical routine therapy combined with group cognitive behavior therapy group based on mindful self-compassion:Group cognitive behavior therapy based on mindful self-compassion
Clinical routine therapy combined with group cognitive behavioral therapy group:Group cognitive behavior therapy
Clinical routine treatment group:None

Sponsors

Beijing Anding Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1.Education level above junior high school 2.Meet DSM-5 diagnostic criteria for depressive disorder 3.Comply with DSM-5 non suicidal self injury diagnostic criteria, and have at least one self injury in the past month 4.Age 12-18 5.The condition is stable, and the drug increment in recent 3 months does not exceed 50% 6.Normal intelligence 7.Willing to try group cognitive behavioral therapy based on self-care, and committed to continuing routine clinical treatment 8.Those who have not received other psychotherapy in recent three months 9.Obtain the informed consent of the patient and guardian, and sign the informed consent form

Exclusion criteria

Exclusion criteria: 1.Serious suicide risk or attempted suicide within the past 6 months 2.With psychotic symptoms 3.Neurodevelopmental disorders, destructive and conduct disorders 4.Serious or unstable physical disease 5.History of traumatic brain injury 6.Have received non-convulsive electroconvulsive therapy within 3 months before enrollment 7.Have participated in meditation intervention in the past, or are receiving other psychotherapy 8.Women who are breastfeeding, pregnant or may become pregnant during the trial 9.Other conditions that psychiatrists think are not suitable for participation

Design outcomes

Primary

MeasureTime frame
Borderline Personality Features;Suicide Ideation;Childhood trauma;Parental rearing style;Self-injury;

Secondary

MeasureTime frame
Depression;Anxiety;

Countries

China

Contacts

Public ContactLiu Jing

Beijing Anding Hospital Affiliated to Capital Medical University

drliujing551@163.com15011413302

Outcome results

None listed

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