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Efficacy of Adjunctive Cerebellar Transcranial Alternating Current Stimulation in Negative Symptoms of Schizophrenia

Efficacy of Adjunctive Cerebellar Theta Transcranial Alternating Current Stimulation in Negative Symptoms of Schizophrenia: A Randomized Sham Controlled Proton Magnetic Resonance Spectroscopy (H1-MRS) Based Study - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058415
Enrollment
40
Registered
2023-10-06
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Health Condition 1: F209- Schizophrenia, unspecified

Interventions

Intervention1: Theta Transcranial Alternating Current Stimulation (tACS), Active.: Theta frequency tACS will be administered using a standard equipment using stringent safety measures. Cerebellum will

Sponsors

Central Institute of Psychiatry
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Diagnosis of Schizophrenia using International Classification of Diseases-11th edition (ICD-11) (WHO, 2019). 2. Patients giving written informed consent. 3. Right-handed patients. 4. Illness duration of equal to or more than 2 years. 5. The Positive and Negative Syndrome Scale for Schizophrenia (PANSS) with 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.

Exclusion criteria

Exclusion criteria: 1. Presence of co-morbid neurological or other psychiatric disorder(s). 2. Patient with co-morbid substance dependence, except nicotine and caffeine. 3. Patients having any metallic implants in the body. 4. Subjects who have received ECT in past 1 month.

Design outcomes

Primary

MeasureTime frame
Cerebellar theta tACS results in a change in the negative symptoms at the end of 10 sessions.Timepoint: Improvement in the scores of PANSS, SANS, CGI at the end of 10 sessions(2 weeks) & 6 weeks as compared to baseline.

Secondary

MeasureTime frame
Changes in the levels of GABA, Glutamate, Glutamine, NAA & NAAG in cerebellum using Proton MR Spectroscopy post theta tACS administration to cerebellum.Timepoint: Baseline, at the end of 10 theta tACS sessions(2 weeks).

Countries

India

Contacts

Public ContactDr Umesh S

Central Institute of Psychiatry

umesh.yes@hotmail.com9771702403

Outcome results

None listed

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