Skip to content

A survey of the survival status of adults with cerebral palsy in Shenzhen

A survey of the survival status of adults with cerebral palsy in Shenzhen

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099517
Enrollment
Unknown
Registered
2025-03-25
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Cerebral palsy

Interventions

Observation group:None

Sponsors

Shenzhen Children’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Adult patients (age >= 18 years) who have been diagnosed with cerebral palsy by a professional medical institution; 2.Possess a household registration in Shenzhen to ensure a certain level of adaptation and exposure to the local medical and social environment; 3.Capable of understanding and signing the informed consent form, possessing a certain level of cognitive and communicative abilities; for community patients with cognitive impairments but who have legal guardians, the informed consent form shall be signed by their legal guardians.

Exclusion criteria

Exclusion criteria: 1.Adult cerebral palsy patients in welfare institutions who are unable to recognize their own actions due to mental, intellectual, or other conditions (persons without capacity for civil conduct) (as determined by professional assessment); 2.Those suffering from other severe mental illnesses (such as schizophrenia) or severe cognitive impairments who are unable to cooperate with the investigation (as determined by professional assessment); 3.Individuals who have experienced a major illness recently (within the past 6 months) or are in the acute phase of a disease, which may affect the accuracy of the survey results; 4.Those currently participating in other clinical trials or research projects that may interfere with this study.

Design outcomes

Primary

MeasureTime frame
Gross motor function;Manual function;Communication function;Eating and drinking function;Functional independence;Emotional function;QOL;

Secondary

MeasureTime frame
Pain;Medical and rehabilitation resources;

Countries

China

Contacts

Public ContactMeihuan Huang

Shenzhen Children’s Hospital

hmh200909@163.com+86 755 83008717

Outcome results

None listed

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