Construction and Clinical Validation Study of a Prediction Model for Depression After Ischemic Stroke
NCT ID: NCT07294274
Last Updated: 2025-12-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
488 participants
OBSERVATIONAL
2025-12-22
2026-07-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
The group of PSD
The patient was diagnosed with PSD.
Group patients based on whether they have been diagnosed with PSD.
Group patients based on whether they have been diagnosed with PSD.
NPSD
The patient was not diagnosed with PSD.
Group patients based on whether they have been diagnosed with PSD.
Group patients based on whether they have been diagnosed with PSD.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Group patients based on whether they have been diagnosed with PSD.
Group patients based on whether they have been diagnosed with PSD.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Admission within 7 days of symptom onset;
* The patient and/or the family members sign a written informed consent form.
Exclusion Criteria
* Individuals with a history of depression, schizophrenia, bipolar disorder, etc;
* Individuals unable to participate in neuropsychological examinations due to hearing im pairments, lack of coordination, or neurological deficits, including se vere aphasia.
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Chongqing Traditional Chinese Medicine Hospital
OTHER
Min Su
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Min Su
Professor of Anesthesiology
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
20251114
Identifier Type: -
Identifier Source: org_study_id