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NCT07680959Enrolling by invitation

Combining HD-tDCS and iTBS in Treating Negative Symptoms of Schizophrenia

The Efficacy of Combined HD-tDCS and iTBS in Treating Negative Symptoms of Schizophrenia

Source: ClinicalTrials.gov · Last updated 9 Jul 2026

Brief summary (registry, in English)

Dysfunction of the dorsolateral prefrontal cortex (DLPFC) is central to the persistence of negative symptoms in schizophrenia. Both HD-tDCS and iTBS targeting the left DLPFC have shown therapeutic benefit. This trial will test the hypothesis that combining HD-tDCS with iTBS yields additive efficacy.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
100 (estimated)
First submitted
26 Jun 2026
Start date
May 2024
Primary completion date
Dec 2027
Lead sponsor
Tri-Service General Hospital (TSGH)
NCT number
NCT07680959

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From May 2024 to the primary completion date, Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients receiving medications that significantly change the seizure threshold;

Other illness

  • Unstable medical conditions;
  • Current psychiatric comorbidity or active substance use disorder (except for tobacco use disorders);
  • History of meningitis, encephalitis, seizures, intracranial neoplasms or surgery, severe head injury or cerebrovascular disease, or a family history of seizures;
  • rTMS or tDCS treatment within the past 6 months as well as a history of electroconvulsive therapy (ECT);
  • A history of suicidal behavior within the past 6 months, or symptom worsening and emergence of suicidal ideation during the screening period.

Other

  • Contraindications for MRI, tDCS or rTMS;
  • Pregnancy or breastfeeding at the time of enrollment;
  • Any skin lesion at the stimulation sites;

Who the study is looking for

  • Subjects diagnosed with DSM-5 schizophrenia or schizoaffective disorder;
  • With a clinical presentation characterized by predominant negative symptoms, as determined by psychiatric assessment and a score of at least 20 on the Negative Symptoms Subscale of the Positive and Negative Syndrome Scale (PANSS);
  • Stable positive and negative symptoms for at least 4 weeks, as documented in medical records and confirmed by clinical judgment and psychiatric interview;

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tri-Service General Hospital
Coordinator of this site? Confirm its status
TaipeiTaiwanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.