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A study of positive psychological group interventions in adolescents with nonsuicidal self-injury

The impact of positive psychological group intervention on emotional regulation and self-efficacy of adolescents with nonsuicidal self-injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079412
Enrollment
Unknown
Registered
2024-01-03
Start date
2024-01-03
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

nonsuicidal self-injury adolescents

Interventions

Group intervention group:Group interventions based on positive psychology theories
General control group:Intervention studies based on general psychoeducation

Sponsors

Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for experimental intervention group and general control group: (1) Han nationality, right-handed, adolescents aged 12-18 years; (2) meet the diagnostic criteria for "nonsuicidal self-injury" recommended by the fifth edition of the American Diagnostic and Statistical Manual of Mental Disorders; (3) According to the Ottawa Self-Injury Scale (OIS), there have been more than 5 self-injury incidents in the past year, and at least 1 self-injurious behavior in the previous 1 month of the group; (4) have never attempted suicide; (5) Patients and their families with informed consent, voluntary participation in clinical trial research, good compliance, voluntary signing of informed consent. Healthy control group inclusion criteria: (1) Han nationality, right-handed, adolescents aged 12-18 years; (2) Have no history of any serious mental or physical illness.

Exclusion criteria

Exclusion criteria: Exclusion criteria for experimental intervention group and general control group: (1) those who do not meet the above diagnostic criteria, have poor compliance, and have not signed informed consent for voluntary participation in experimental research; (2) have a history of substance abuse; (3) Have a history of brain trauma or other serious diseases; (4) have a history of any other mental health disorder; (5) those who are not motivated by treatment; (6) Patients with claustrophobia or other metal substances containing implants such as metal dentures, pacemakers, artificial joints, insulin pumps, etc. that cannot be obtained, and patients with claustrophobia. Exclusion criteria for healthy controls: same as experimental intervention group.

Design outcomes

Primary

MeasureTime frame
Chinese version of the Ottawa Self-harm Scale;Functional magnetic resonance imaging;

Secondary

MeasureTime frame
anxiety;depression;

Countries

China

Contacts

Public ContactChang Shuying

Henan Provincial People's Hospital; Zhengzhou University

Csy69222@163.com+86 138 3829 5990

Outcome results

None listed

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