Beta-band brain stimulation to reduce impulsive self-injury in teens
Official title: The Impact of Beta-band Transcranial Alternating Current Stimulation (tACS) on Impulse Inhibition in Adolescents With Non-suicidal Self-injury
Run by Anhui Medical University · NCT07152925 · Data updated 2026-11-12
This trial will try twice-daily beta-frequency transcranial alternating current stimulation versus sham in adolescents with non-suicidal self-injury to see if it reduces self-harm episodes and impulsivity and is safe.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 12 Years to 22 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Anhui Medical University Academic / other |
| Locations | 1 site (Hefei, Anhui) |
| Status | Recruiting |
| Started | March 1, 2025 |
| Main results expected | May 31, 2026 |
| Study ends | May 31, 2026 |
| Registry record updated | September 3, 2025 |
| Trial ID | NCT07152925 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are right-handed adolescents aged 12–18 who meet DSM-5 criteria for NSSI with at least five documented episodes and at least one incident in the past month, have sufficient education and normal or corrected binocular vision, and can participate with guardian consent.
✕Probably not a fit
Patients with prior suicide attempts, significant neurological conditions (e.g., epilepsy, brain surgery, intracranial metal), severe psychiatric comorbidity or substance use disorder, MoCA score below 26, or who cannot attend daily visits are unlikely to benefit or be eligible.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional trial compares active beta-frequency transcranial alternating current stimulation (tACS) with sham stimulation in adolescents who meet DSM-5 criteria for non-suicidal self-injury (NSSI). Participants receive two stimulation sessions per day, four hours apart, for seven consecutive days (14 sessions total), with clinical scales, behavioral tasks, and eye-tracking performed before and after the intervention. Self-injury episodes and any adverse reactions are recorded continuously, and cognitive and medical screening (e.g., MoCA, neurological history) determine eligibility. The primary outcomes focus on changes in impulse inhibition and the safety/tolerability of beta-band tACS.
Why it matters
Potential benefit: If successful, beta-band tACS could provide a short, noninvasive method to reduce impulsivity and the frequency of self-injury in adolescents.
How similar studies have gone: Small studies of noninvasive brain stimulation (tDCS/tACS) have shown mixed but occasionally promising effects on impulsivity and mood, while beta-band tACS specifically for adolescent NSSI remains a relatively novel and unproven approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 1\) Meet the proposed diagnostic criteria for non-suicidal self-injury (NSSI) in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), with ≥5 documented self-injury episodes and at least one incident within the past month as assessed by the Adolescent Non-Suicidal Self-Injury Assessment Questionnaire (ANSAQ); 2) Aged 12-18 years; 3) Right-handed; 4) Possess formal education experience sufficient to comprehend experimental protocols; 5) Normal or corrected-to-normal binocular visual acuity; 6) Voluntarily participate with legal guardians providing written informed consent. Exclusion Criteria: * 1\) Montreal Cognitive Assessment (MoCA) score \< 26; 2) History of suicide attempt(s); 3) Medical history of epilepsy, brain surgery, intracranial tumors, metal implants in the skull, or clinically significant head trauma; 4) History of substance use disorder, brain injury, severe somatic diseases, psychiatric disorders, or comorbid DSM-5 psychiatric conditions; 5) Prior receipt of transcranial direct current stimulation (tDCS), transcranial alternating current stimulation (tACS), or repetitive transcranial magnetic stimulation (rTMS) within the past 3 months
Where it's running
-
School of Mental Health and Psychological Sciences, Anhui Medical University
Hefei, Anhui, China Recruiting
Study contacts
- Study coordinator: Meiling Wang, bachelor
- Email: 1605280093@qq.com
- Phone: +86 136 4707 0027
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Temporal interference stimulation for non‑suicidal self‑injury in adolescent depression
This trial will test whether temporal interference stimulation (TIS) can reduce non‑suicidal self‑injury in adolescents and young adults (ages 12–22) with major depressive disorder compared with a sham treatment.
-
Ear vagus nerve priming plus gentle alternating brain stimulation for teens with non-suicidal self-injury
This study will test whether brief transcutaneous auricular vagus nerve stimulation (taVNS) given before mild 10 Hz transcranial alternating current stimulation (tACS) over the left dlPFC can reduce self-injury-related attention biases, impulsivity, and self-injury behaviors in adolescents aged 12–18 with non-suicidal
-
Medical and psychiatric profiling of adults admitted to general adult psychiatry wards
This project will collect questionnaires, rating scales, and case-note information from adults admitted to general adult psychiatry wards to see what their physical and mental health profiles look like.
-
Long-term psychotropic medication effects on eye movements measured with the Gaize VR headset
This project will test whether the Gaize VR headset can detect eye-movement patterns associated with long-term use of prescribed psychotropic medications in adults.
-
Psychiatric Symptoms and Quality of Life in Graft-versus-Host Disease
This project will see if psychiatric symptoms like depression are linked to GvHD symptom severity and health-related quality of life in adults with graft-versus-host disease.
-
Digital twins to classify mental health patterns in adults with diabetes
This project will try to create 'digital twin' profiles that combine glucose, mood, and behavior data to track mental health patterns in adults with diabetes.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.