Skip to content

Study on Expanding the Clinical Indications of an EEG-Based Rehabilitation Training Device for Motor Dysfunction in Children with Central Nervous System Injury

Study on Expanding the Clinical Indications of an EEG-Based Rehabilitation Training Device for Motor Dysfunction in Children with Central Nervous System Injury

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118500
Enrollment
Unknown
Registered
2026-02-06
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

Motor dysfunction of the limbs caused by non-progressive central nervous system injury in children

Interventions

Upper limb control group:Conventional rehabilitation therapy combined with NMES treatment
Upper limb experimental group:Conventional rehabilitation therapy combined with BCI-FES treatment
Lower limb control group:Conventional rehabilitation therapy combined with NMES treatment
Lower limb experimental group:Conventional rehabilitation therapy combined with BCI-FES treatment

Sponsors

Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1.Age between 6 and 18 years, regardless of sex; 2.Diagnosed with non-progressive central nervous system injury of the brain, including but not limited to cerebral palsy and sequelae of traumatic brain injury; 3.Disease duration >= 1 month; 4.Presence of unilateral upper or lower limb motor dysfunction, with muscle strength of the wrist extensor or tibialis anterior < grade 3, and GMFCS level I–III for participants in the lower limb group; 5.Able to understand and follow instructions; 6.Written informed consent obtained from the child’s legal guardian.

Exclusion criteria

Exclusion criteria: 1.Presence of severe cognitive impairment, frequent epileptic seizures, or other conditions unsuitable for EEG recording; 2.Received botulinum toxin injection or orthopedic surgery within the past 6 months; 3.Implanted with devices sensitive to electrical stimulation, such as cardiac pacemakers or deep brain stimulation electrodes; 4.Currently participating in other interventional clinical studies.

Design outcomes

Primary

MeasureTime frame
Functional assessment of the affected limb;Task-based fNIRS;Gait analysis in the lower limb group;Task-based EEG;

Secondary

MeasureTime frame
EEG training indicators;Safety evaluation;Physical examination of limb motor function;

Countries

China

Contacts

Public ContactMin Shen

Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine

minshen223@qq.com+86 21 38088320

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026