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Efficacy of parse-initiated iTBS on non-fluent aphasia and fNIRS brain network characteristics based on the dual-stream language model

Efficacy of parse-initiated iTBS on non-fluent aphasia and fNIRS brain network characteristics based on the dual-stream language model

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095244
Enrollment
Unknown
Registered
2025-01-03
Start date
2024-07-29
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

non-fluent aphasia

Interventions

Case group:None
Initiated iTBS group:cTBS+ iTBS
Non-initiated iTBS group:false cTBS+ iTBS
False Stimulus Group:false cTBS+ false iTBS
Healthy control group:None

Sponsors

Shanghai Second Rehabilitation Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.All met the criteria of 'Diagnostic Points of Various Cerebrovascular Diseases' formulated by the Fourth National Conference on Cerebrovascular Diseases of the Chinese Medical Association in 1995; 2.Right-handed, non-fluent aphasia as assessed by Western Aphasia Battery (WAB) after the onset of the disease; 3.Duration of the disease from 2 weeks to 6 months; 4.Chinese as the first language, with an education level of primary school or above; 5.Ability to remain sitting independently for more than 30 min, can cooperate to complete the language function assessment and fNIRS test, and have no obvious memory and intellectual disabilities; 6.Patient or family members signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Concomitant other neurodegenerative diseases, such as Parkinson's disease, etc. 2. application of drugs that change the excitability of the cerebral cortex (antiepileptic drugs), sleeping pills, benzodiazepines, etc. 3. history of psychiatric anomalies; 4. epilepsy; 5. severe cardiac, hepatic, renal dysfunction or other serious physical diseases; 6. coma, unable to cooperate with the examination and treatment; 7. auditory or visual deficiencies that may affect the assessment and treatment; 8. According to the safety guideline, rTMS is not suitable for those who have metal foreign objects or other electronic devices implanted in the body.

Design outcomes

Primary

MeasureTime frame
Functional Near Infrared (fNIRS) Detection;

Secondary

MeasureTime frame
Westemm Aphasia Battery;

Countries

China

Contacts

Public ContactJiayi Xia

Shanghai Second Rehabilitation Hospital

532821681@qq.com+86 17721485860

Outcome results

None listed

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