Clinical trial Recruiting at 1 site Observational

Predicting depression risk after an ischemic stroke

Official title: Construction and Clinical Validation Study of a Prediction Model for Depression After Ischemic Stroke

Run by First Affiliated Hospital of Chongqing Medical University · NCT07294274 · Data updated 2026-11-12

This project will try to use machine learning on clinical and other patient data to predict which people hospitalized with an acute ischemic stroke will develop depression.

Quick facts

Study typeObservational
SexAll
Enrollment488 (estimated)
SponsorFirst Affiliated Hospital of Chongqing Medical University
Academic / other
Locations1 site (Chongqing)
StatusRecruiting
StartedNovember 1, 2025
Main results expectedJuly 20, 2026
Study endsJuly 20, 2026
Registry record updatedFebruary 5, 2026
Trial IDNCT07294274 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults hospitalized with acute ischemic stroke within seven days of symptom onset who can complete neuropsychological testing and provide informed consent.

Probably not a fit

Patients with a prior history of major psychiatric illness, severe cognitive impairment, impaired consciousness, or major communication deficits such as severe aphasia may not benefit from or be eligible for the model.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study will collect multidimensional clinical, demographic, and neuropsychological data from patients admitted with acute ischemic stroke and group them by whether they develop post-stroke depression. Researchers will apply machine learning methods to these data to build and clinically validate a risk prediction model for post-stroke depression. The goal is to enable early, individualized risk estimates based on routinely available indicators from patients admitted within seven days of symptom onset. Exclusion criteria include prior major psychiatric disorders, severe cognitive impairment, impaired consciousness, or inability to complete neuropsychological testing.

Why it matters

Potential benefit: If successful, the model could help clinicians identify high-risk patients early so they can provide targeted monitoring, preventive support, or timely treatment to improve recovery and quality of life.

How similar studies have gone: Early machine-learning work predicting post-stroke outcomes has shown promise, but robust, externally validated models specifically for post-stroke depression remain limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients with acute ischemic stroke;
* Admission within 7 days of symptom onset;
* The patient and/or the family members sign a written informed consent form.

Exclusion Criteria:

* Confusion of consciousness,severe cognitive impairment, etc
* 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.

Where it's running

  • The First Affiliated Hospital of Chongqing Medical University
    Chongqing, China
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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  • Building physical capacity after chronic stroke

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  • Effects of natural light on stroke recovery complications

    This study tests if using natural light during rehab can help stroke patients feel less depressed and tired as they recover.

    Recruiting Copenhagen University Hospital, Rigshospitalet · Glostrup Municipality, Capital Region · NCT06922409

  • Telephone/video behavioral activation to prevent depression after a first stroke in low-income older adults

    This project will test whether coaching-style behavioral activation delivered by trained lay counselors over phone or video can prevent depression in low-income older adults who recently had a first stroke and currently have mild or no depressive symptoms.

    Recruiting The University of Texas Health Science Center, Houston · Houston, Texas · NCT06864715

  • Zuranolone (allopregnanolone) for post-stroke depression

    This trial will test whether a 14-day course of oral zuranolone is safe, well tolerated, and can reduce moderate to severe depression in adults 21–65 who developed depression within a year after a stroke.

    Recruiting Phase 2 Duke University · Durham, North Carolina · NCT06759558

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.