Enhanced Recovery After Surgery Using TMS on Cerebellar Language Area for Brain Tumor Patients
Through the Navigation Transcranial Magnetic Stimulation Over the Language Key Areas of Cerebellar to Enhance Language Function Recovery After Brain Tumor Resection
At present, the incidence of language dysfunction in patients with brain language area tumor in the first month after operation was 20%-40%. The investigator's team has confirmed and found that bilateral cerebellar VIIa lobules are the critical areas of cerebellar which is closely related to the language function of the patients. This study aims at enhancing language function recovery after surgery through the transcranial magnetic stimulation stimulates the key areas of cerebellar.
This study is a prospective, randomized, double-blind, multi-center clinical trial in which participants with postoperative aphasia in the brain-language region tumors of three neurosurgery departments, Huashan Hospital, Shanghai Jing'an Center Hospital and Huashan Hospital North Hospital. Participants were randomly divided into Intervention group and control group. Before transcranial magnetic stimulation treatment, the two groups were required to conduct language behavior assessment and magnetic resonance imaging data. Participants in both groups were given 10 consecutive days bilateral cerebellar VIIa lobules Theta Burst Stimulation from one week after surgery and received speech rehabilitation training after stimulation.
The investigators collect patients MRI data and language behavioral assessment scores at 1week post operation and 1 month after the operation and 3 months after the operation. Subsequently, three MRI data and language behavioral assessment scores were processed and statistically analyzed to compare the differences between the two groups
Descripción general del estudio
Estado
Intervención / Tratamiento
Descripción detallada
Intervention group: Intermittent Theta Burst Stimulation(Positive stimulation) is used in right cerebellar VIIa lobule. Continuous Theta Burst Stimulation(Negative stimulation) is used in left cerebellar VIIa lobule. The stimulation intensity was 80% Rest Motor Threshold.According to the patients' condition, age and tolerance,the intensity should be adjusted.
Control group: The investigators use with fake stimulation , the appearance is the same as the magnetic stimulator used in the experimental group, and the stimulation will also make sounds, but no magnetic field effect, the stimulation mode is the same as the intervention group.
Subsequently, The investigators collect patients MRI data and language behavioral assessment scores at 1week post operation and 1 month after the operation and 3 months after the operation.three times MRI data and language behavioral assessment scores were processed and statistically analyzed to compare the differences between the two groups from the cerebellar spontaneous neurological activity level (ALFF), cerebellar gray matter volume, functional connectivity of cerebellar network and language behavioral score.
Tipo de estudio
Inscripción (Anticipado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Jinsong Wu, MD
- Número de teléfono: 86-021-52887200
- Correo electrónico: wjsongc@126.com
Copia de seguridad de contactos de estudio
- Nombre: Tianming Qiu, MD
- Número de teléfono: 86-021-52887200
- Correo electrónico: Tianming2100@126.com
Ubicaciones de estudio
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Shanghai
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Shanghai, Shanghai, Porcelana, 200040
- Reclutamiento
- Huashan Hospital affiliated to Fudan University
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Contacto:
- Jinsong Wu, MD
- Número de teléfono: 86-021-52887200
- Correo electrónico: wjsongc@126.com
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Investigador principal:
- Jinsong Wu, MD
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Sub-Investigador:
- Dongxiao Zhuang, MD
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Sub-Investigador:
- Tianming Qiu, MD
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Sub-Investigador:
- Jie Zhang, MD
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Contacto:
- Tianming Qiu, MD
- Número de teléfono: 86-021-52887200
- Correo electrónico: Tianming2100@126.com
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Sub-Investigador:
- ruiping Hu, MD
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Sub-Investigador:
- Qiao Shan, MD
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Sub-Investigador:
- Chengxin Ma, MD
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Shanghai, Shanghai, Porcelana, 200040
- Reclutamiento
- Shanghai Jing'an Central Hospital
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Contacto:
- Qingyang Luo, MD
- Número de teléfono: 021-61578000
- Correo electrónico: luoqingyang529@sina.com
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Language dysfunction after brain tumor surgery (aphasia quotient,AQ)< 93.8
- Chinese mother tongue
- Right handedness confirmed by Edinburgh Handedness Scale
- Tumor patients with linguistic region involvement in the dominant hemisphere
- Karnofsky Performance Status (KPS)< 70
- Voluntary participation in this project
Exclusion Criteria:
- Patients with frequent epileptic seizures (> 2 epilepsy episodes per week)
- Previous implants of metal pacemakers, stimulators, hearing aids, dentures, and insulin pumps or claustrophobia
- People with a history of psychiatric disorders
- Patients with severe medical diseases
- Patients with Alzheimer's disease and Parkinson's disease. Medical diseases
- Pregnant women
- Other clinical trials in the same period.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Triple
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Comparador activo: Theta Burst Stimulation
Intervention group: ten consecutive days bilateral cerebellar VIIa lobules Theta Burst Stimulation. Intermittent Theta Burst Stimulation(Positive stimulation) is used in right cerebellar VIIa lobule.Each stimulus had three 50 Hz monopulses, which were repeated every 200 ms. Each stimulation continued for 2 seconds and rested for 8 seconds. The total intervention time was 200s (600 pulses) Continuous Theta Burst Stimulation(Negative stimulation) is used in left cerebellar VIIa lobule,three 50 Hz monopulses in each stimulus, each with an interval of 200 ms, and each intervention lasted 40s (600 pulses). The stimulation intensity was 80% Rest Motor Threshold.According to the patients' condition, age and tolerance,the intensity should be adjusted. |
1.Patients were given 10 consecutive days bilateral cerebellar VIIa lobules Theta Burst Stimulation which was a special mode of Transcranial magnetic stimulation from one week after surgery Intermittent Theta Burst Stimulation(Positive stimulation) is used in right cerebellar VIIa lobule.Each stimulus had three 50 Hz monopulses, which were repeated every 200 ms.
Each stimulation continued for 2 seconds and rested for 8 seconds.
The total intervention time was 200s (600 pulses) Continuous Theta Burst Stimulation(Negative stimulation) is used in left cerebellar VIIa lobule,three 50 Hz monopulses in each stimulus, each with an interval of 200 ms, and each intervention lasted 40s (600 pulses).
Otros nombres:
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Comparador falso: sham Theta Burst Stimulation
sham group: we flip coil to make fake stimulation, the stimulation will also make sounds, but no magnetic field effect, the stimulation mode is the same as the intervention group.
|
1.Patients were given 10 consecutive days bilateral cerebellar VIIa lobules Theta Burst Stimulation which was a special mode of Transcranial magnetic stimulation from one week after surgery Intermittent Theta Burst Stimulation(Positive stimulation) is used in right cerebellar VIIa lobule.Each stimulus had three 50 Hz monopulses, which were repeated every 200 ms.
Each stimulation continued for 2 seconds and rested for 8 seconds.
The total intervention time was 200s (600 pulses) Continuous Theta Burst Stimulation(Negative stimulation) is used in left cerebellar VIIa lobule,three 50 Hz monopulses in each stimulus, each with an interval of 200 ms, and each intervention lasted 40s (600 pulses).
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Boston naming test
Periodo de tiempo: Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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The change of Boston naming test scores is being assessed
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Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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MMSE
Periodo de tiempo: Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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The change of Mini-mental State Examination scores is being assessed
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Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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ABC
Periodo de tiempo: Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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Aphasia Battery of Chinese，Conclude naming, repeating, comprehend and spontaneous speech test，The change of ABC scores is being assessed
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Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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ALFF
Periodo de tiempo: Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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The change of Cerebellar spontaneous neurological activity level is being assessed
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Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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Cerebellar gray matter volume
Periodo de tiempo: Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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The change of Cerebellar gray matter volume is being assessed
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Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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Functional connectivity of cerebellar network
Periodo de tiempo: Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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The change of functional connectivity of cerebellar network is being assessed
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Change from postoperative 1 week to postoperative 1month & postoperative 3 months
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Jinsong Wu, MD, Huashan Hospital
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- KY2018-395
Plan de datos de participantes individuales (IPD)
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Información sobre medicamentos y dispositivos, documentos del estudio
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