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Ultra-early precise screening and application of cerebral palsy based on multimodal fusion

Ultra-early precise screening and application of cerebral palsy based on multimodal fusion

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094667
Enrollment
Unknown
Registered
2024-12-25
Start date
2025-01-01
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

Cerebral palsy

Interventions

Gold Standard:At present, the main diagnostic methods for cerebral palsy include whole-body motor quality assessment (GMs), Hammersmith infant neurological examination (HINE), and infant neurodevelopm
Index test:GMs, HINE, MRI, and infant neurodevelopmental assessment tools and professional clinical diagnosis

Sponsors

Children's Hospital,Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 1 Years

Inclusion criteria

Inclusion criteria: 1. Infants aged 3 days to 5 months, regardless of gender; 2.High-risk factors for cerebral palsy and neurodevelopmental impairment: including multiple pregnancies, intracranial hemorrhage, intracranial infection, neonatal hypoxic ischemic encephalopathy, perinatal asphyxia, low birth weight, hyperbilirubinemia, etc; 3.Abnormal neurological examination: such as abnormal muscle tone, abnormal posture, abnormal reflexes; 4.Two qualified senior therapists who have completed the GMs Trust training course determine the high-risk infants of cerebral palsy using the gold standard assessment for cerebral palsy - the Global Movement Assessment Scale (GMs), including the presence of global movement disorder, spastic synergy, monotony, and asymmetry before term or during the fetal movement stage,the presence of abnormal hyperactivity and the absence of restlessness; 5.Children aged 1 and 2 have a clear follow-up outcome: determined to have cerebral palsy, including the following four essential conditions: (1) persistent central motor dysfunction;(2).abnormal development of movement and posture;(3). abnormal muscle tone and muscle strength;(4). abnormal development of reflexes; 6. Have not received any relevant drugs within the past 3 months; 7.The patient and parents agree to participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Currently participating in other clinical trials; 2.Diagnosed with Rett syndrome or fragile X syndrome through genetic testing or clinical diagnosis; 3.Patients with severe or unstable physical conditions, including cardiovascular diseases, tumors, kidney diseases, secretory diseases (including thyroid dysfunction), gastrointestinal diseases, hematological diseases, and neurological diseases; 4.The attending physician or researcher believes that there are other circumstances that are not suitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
cerebral palsy;

Countries

China

Contacts

Public ContactJinpiao Zhu

Children's Hospital,Zhejiang University School of Medicine

zhujinpiao@zju.edu.cn+86 571 81732401

Outcome results

None listed

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