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The construction and empirical study of a risk prediction model for post-stroke depression

The construction and empirical study of a risk prediction model for post-stroke depression

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100052912
Enrollment
Unknown
Registered
2021-11-06
Start date
2021-11-04
Completion date
Unknown
Last updated
2022-08-23

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

Conditions

Post-stroke depression

Interventions

Post-stroke depression VS post-stroke without depression group:none

Sponsors

Jieyang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of stroke in "Key Points for the Diagnosis of Various Cerebrovascular Diseases", and be diagnosed with cerebral hemorrhage or cerebral infarction by head CT or MRI imaging; 2. Aged >= 18 years; 3. Within 1 week of stroke onset, clear consciousness and stable condition upon admission, and have independent understanding of other people's language or behavior.

Exclusion criteria

Exclusion criteria: 1. Combined with serious organic diseases such as heart, lung, liver, kidney, etc., or diseases such as blood diseases and malignant tumors; 2. Those with previous organic and functional mental disorders, including depressive disorders; 3. Previous traumatic brain injury, Parkinson's disease and other organic brain lesions or senile dementia, vascular dementia and other neurodegenerative diseases that can lead to depression; 4. Those who have a history of depression or antidepressant medication in the past; 5. Long-term use of drugs or drug abusers that can cause depression; 6. History of major mental trauma in the past 1 year; 7. Voluntarily request to withdraw from the study or be lost to follow-up; 8. Incomplete collection of case data due to the aggravation of the disease and the inappropriateness of continuing research or accidental death.

Design outcomes

Primary

MeasureTime frame
Depression;neurological impairment;cognitive impairment;social support;resilience;activity of daily life;sleeping quality;general data;clinical data of stroke;laboratory examination indexes;

Countries

China

Contacts

Public ContactXie Man

Jieyang People's Hospital

Man.Xie@hotmail.com+86 663 8660802

Outcome results

None listed

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