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The Study on Neuroimaging Characteristics of Emotional Dysregulation in Adolescents with Non-Suicidal Self-Injury

The Study on Neuroimaging Characteristics of Emotional Dysregulation in Adolescents with Non-Suicidal Self-Injury - Imaging Characteristics of Emotional Dysregulation in NSSI Adolescents

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123799
Enrollment
Unknown
Registered
2026-04-29
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

Non-Suicidal Self-Injury

Interventions

Non-suicidal Self Injury Group:This study is an observational study and does not involve any intervention.
Health Control Group:This study is an observational study and does not involve any intervention.

Sponsors

Shanghai Pudong New Area Mental Health Center (Mental Health Center Affiliated with Tongji University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
11 Years to 19 Years

Inclusion criteria

Inclusion criteria: Non-suicidal Self-Injury (NSSI) Group: 1. Assessed by two psychiatrists with intermediate-level or higher qualifications using the Self-Injurious Thoughts and Behaviors Interview (SITBI, Chinese version), and meeting the NSSI diagnostic criteria listed in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) (NSSI occurring on >=5 days within the past 12 months, with self-injury behaviors primarily motivated by non-suicidal intent); 2. Aged 11–19 years, right-handed; 3. Possess the cognitive ability to complete structured interviews and self-report questionnaires, and be able to follow research instructions to complete MRI scanning procedures; 4. No contraindications for MRI scanning; no history of modified electroconvulsive therapy, medication, or psychotherapy/counseling within the past 3 months; 5. Informed consent obtained from the participant and their guardian; voluntary participation. Health Control Group (HC): 1. Aged 11–19 years, right-handed, matched with the NSSI group in terms of age, gender, and educational level; 2. Confirmed via the SITBI interview to have no lifetime history of NSSI, suicidal ideation, plans, or behaviors; 3. Confirmed via the Mini-International Neuropsychiatric Interview (MINI) to have no history of past or current psychiatric disorders and no significant psychiatric symptoms in the past month; 4. Possess the cognitive ability to complete structured interviews and self-report questionnaires, and be able to follow study instructions to complete MRI scanning procedures; 5. Informed consent obtained from the participant and their guardian; voluntary participation.

Exclusion criteria

Exclusion criteria: 1. A current or past diagnosis of a severe mental disorder, such as schizophrenia, schizotypal disorder, schizoaffective disorder, delusional disorder, or bipolar disorder, according to DSM-5 criteria; 2. A mental disorder caused by a physical medical condition or by the use of psychoactive substances; 3. Symptoms caused by substance abuse; 4. Individuals with traumatic brain injury, epilepsy, or other known organic central nervous system disorders; 5. Individuals who have continuously taken antipsychotics, antidepressants, mood stabilizers, or similar medications for more than 2 weeks within the past 3 months.

Design outcomes

Primary

MeasureTime frame
Brain imaging markers;NSSI trait indicators;

Secondary

MeasureTime frame
Psychological trait indicators;

Countries

China

Contacts

Public ContactFazhan Chen

Shanghai Pudong New Area Mental Health Center (Mental Health Center Affiliated with Tongji University)

develop909@163.com+86 21 6830 6699

Outcome results

None listed

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