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Effects of cognitive behavioural therapy incorporating interoception on adolescents With Nonsuicidal Self-Injury: a randomised controlled trial

Effects of cognitive behavioural therapy incorporating interoception on adolescents With Nonsuicidal Self-Injury: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089209
Enrollment
Unknown
Registered
2024-09-04
Start date
2024-09-25
Completion date
Unknown
Last updated
2024-09-09

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

Conditions

Nonsuicidal Self-Injury

Interventions

Psychological intervention group:Individual Intervention Sessions
Treatment As Usual group:Treatment-as-usual(TAU)

Sponsors

Vanke School of Public Health, Tsinghua University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: (1) Age 12-18 years; (2)Non-suicidal self-injurious behaviour on at least 5 days in the past year, and non-suicidal self-injurious behaviour in the past month; (3) Willingness to audio- or video-record interventions; (4) Participation in the study was voluntary and required informed consent from the guardian, who signed an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Exclusion of people assessed by a doctor to be at high current risk of suicide; (2) Exclusion of patients with a diagnosis of eating disorders, mania, obsessive-compulsive disorder, neurodevelopmental disorders, substance abuse or psychotic disorders; (3) Exclusion of patients who do not wish to be audio or video recorded during the intervention; (4) Exclusion of systematic psychological treatment (including psychotherapy and counseling, etc.) in the last 3 months; (5) Exclusion of physiotherapy (including electroconvulsive therapy, transcranial magnetic stimulation, etc.) in the last 3 months; (6) Exclusion of patients who refused to sign the informed consent form or were unwilling to participate in the program, or who were unwilling to let their guardians know and sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Non-suicidal self-injurious behaviors ;

Secondary

MeasureTime frame
Non-suicidal self-injurious thoughts;Self-injury addiction;Self-injurious impulsivity;Future cessation of NSSI aspirations;The Patient Health Questionnaire36;Generalized anxiety disorder ;Interoception;Suicidal Behaviors;

Countries

China

Contacts

Public ContactRunsen Chen

Vanke School of Public Health, Tsinghua University

runsenchen@tsinghua.edu.cn+86 177 6199 2070

Outcome results

None listed

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