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High-precision transcranial direct current stimulation therapy for adolescent patients with tic disorders based on inflammatory markers and brain function network analysis: a randomized, double-blind, pseudo-controlled, cross-control clinical study

High-precision transcranial direct current stimulation therapy for adolescent patients with tic disorders based on inflammatory markers and brain function network analysis: a randomized, double-blind, pseudo-controlled, cross-control clinical study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102148
Enrollment
Unknown
Registered
2025-05-09
Start date
2024-11-19
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

Tic disorder

Interventions

Immunosusceptible group (Study One):Cytokine assays
Normal group (Study One):Cytokine assays
Treatment group (Study Two):Transcranial direct current stimulation
Control group (Study Two):Pseudo-stimulation of transcranial direct current stimulation

Sponsors

the Affiliated Brain Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Study 1: (1) Patients who attended the outpatient clinic of the Children's Center of Nanjing Brain Hospital and met the DSM-5 CTD/TS diagnostic criteria; (2) Age 4~18 years old; (3) Participants and their parents have signed a written informed consent form; (4) Right hand. Study 2: (1) Patients who were admitted to the Children's Mental Health Research Center of the Brain Hospital of Nanjing Medical University and met the DSM-5 CTD/TS diagnostic criteria; (2) Age 6~18 years old; (3) Previous EEG examination is normal (official report issued by a tertiary hospital); (4) Patients who are on medication to control tics, as long as the dose is stable for at least six weeks before participation and there is no planned change during the course of the study, can also be included; (5) Participants and their parents have signed written informed consent; (6) Right hand.

Exclusion criteria

Exclusion criteria: Study 1: (1) Presence of severe mental disorders, such as schizophrenia, bipolar disorder, major depressive disorder, and severe mental retardation; (2) Have neurological diseases and serious physical diseases. Study 2: (1) Contraindications to tDCS (including: implantable electronic devices in vivo, implanted metal cranial devices, history of traumatic brain injury, scalp lesions at the proposed electrode site, history of epilepsy); (2) Presence of severe mental disorders, such as schizophrenia, bipolar disorder, severe depression, and severe mental retardation; (3) Have a history of neurological diseases and serious physical diseases; (4) Those who cannot cooperate with the completion of the test and follow-up.

Design outcomes

Primary

MeasureTime frame
Cytokine;Yale Global Tic Severity Scale;Cytokines;Resting-state brain network analysis;Yale Global Tic Severity Scale;

Secondary

MeasureTime frame
Age of onset;Course of disease;Children's Sleep Habits Questionnaire;Depression Self-rating Scale for Children;The Screen for Child Anxiety Related Emotional Disorders;Swanson, Nolan, and Pelham Questionnaire — Version IV, SNAP-?;Cognitive Flexibility Scale;Parenting Stress Index - Short Form;

Countries

China

Contacts

Public ContactKe Xiaoyan

the Affiliated Brain Hospital of Nanjing Medical University

1303283950@qq.com+86 133 0517 6562

Outcome results

None listed

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