Skip to content

A randomized controlled trial on the efficacy of BCI-based melodic intonation therapy AI training on speech dysfunction after brain injury

A randomized controlled trial on the efficacy of BCI-based MIT AI training on speech dysfunction after brain injury - The neural mechanism of the MIT based on music therapy to aphasia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114153
Enrollment
Unknown
Registered
2025-12-08
Start date
2024-08-08
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Non-fluent aphasia after stroke

Interventions

Intervention group:In the intervention group (AI-assisted MIT treatment), ear canal BCI+EEG was used for monitoring collection and treatment, 30 minutes each time, 5 times a week, for a total of 8 wee
Control group:n the control group (ST treatment), ear canal BCI+EEG was used for monitoring collection and treatment for 30 minutes each time, 5 times a week for 8 weeks

Sponsors

Beijing Bo'ai Hospital, China Rehabilitation Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: The patient has a history of left craniocerebral injury, left stroke, and left glioma surgery. They meet the diagnostic criteria for speech dysfunction, presenting with reduced spontaneous speech and impaired expression. The inclusion criteria include age between 18 and 70 years old, hearing range of 10-60dB (500-3000Hz), willingness to participate in expressive activities, ability to coordinate movements to some extent, retention of certain cognitive abilities, and tolerance for sitting training. Informed consent was obtained from both patients and their families for their participation in this study.

Exclusion criteria

Exclusion criteria: Severe cognitive impairment; Patients with epilepsy and malignant arrhythmia; In cases where patients are contraindicated for MRI or unable to tolerate functional MRI, the study can be terminated promptly upon any changes in their condition, hospital discharge, or voluntary withdrawal.

Design outcomes

Primary

MeasureTime frame
functional magnetic resonance imaging, fMRI;Boston Diagnostic Aphasia Examination, BDAE;

Countries

China

Contacts

Public ContactXiaoying Zhang

Beijing Bo'ai Hospital, China Rehabilitation Research Center

389608661@qq.com+86 10 8757 7036

Outcome results

None listed

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