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Improvement in Negative and Cognitive Symptoms of Early Onset Schizophrenia patients by using H1 Deep Transcranial Magnetic Stimulation

Efficacy of Adjuvant H1 Deep Transcranial Magnetic Stimulation (dTMS) for Treatment of Negative and Cognitive Symptoms of Early Onset Schizophrenia: A Sham Controlled Functional Magnetic Resonance Imaging and Cortical Plasticity Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/083875
Enrollment
40
Registered
2025-04-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: F20- Schizophrenia

Interventions

Intervention1: H1 Deep Transcranial Magnetic Stimulation (dTMS), active: The helmet with H1 dTMS coil will be placed on the head of the patient. It will be adjusted such that, the maximal stimulation

Sponsors

Central Institute of Psychiatry
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosis of Schizophrenia using Clinical descriptions and diagnostic requirements for ICD-11 mental, behavioral and neurodevelopmental disorders (CDDR) (ICD-11 CDDR, World Health Organization, 2019). 2. Age between 10- 20 years of either sex. 3. Right-Handed 4. Onset of Illness before the age of 18 years. 5. The Positive and Negative Syndrome Scale for Schizophrenia (PANSS) negative symptoms score of more than 15. 6. Scale for Assessment of Negative Symptoms (SANS) score more than 20. 7. Calgary Depression Scale for Schizophrenia (CDSS) score less than 7. 8. Patients providing assent/consent and written informed consent provided by parents/caregivers for the study.

Exclusion criteria

Exclusion criteria: 1. Presence of co-morbid neurological or other psychiatric disorder(s). 2. Patients with co morbid substance dependence, except nicotine and caffeine. 3. Having any metallic implants/parts in body. 4. Subjects who have received ECT or any type of Neuromodulation in past 6 months.

Design outcomes

Primary

MeasureTime frame
Improvement in negative and cognitive symptoms of early onset schizophrenia as measured by PANSS, SANS, BACS, CGISCH after receiving adjuvant H1 dTMSTimepoint: Primary Outcomes are assessed at baseline, 2 and 6 weeks after intervention

Secondary

MeasureTime frame
Change in BOLD activity of Pre-Frontal Cortex, cortical plasticity, and resting state fMRI at baseline and after application of H1 dTMS.Timepoint: Secondary outcomes are assessed at baseline and at 2 weeks

Countries

India

Contacts

Public ContactDr Nishant Goyal

Central Institute of Psychiatry

nishantgoyal.cip@gov.in9431171162

Outcome results

None listed

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