Stroke
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Age >= 18 years, any gender; 2. Clinical manifestations and imaging examination (CT or MRI) confirm stroke, meeting the diagnostic criteria; 3. In the acute or early recovery phase of stroke (generally within 7–14 days after onset) and hospitalized; 4. Vital signs stable, condition stable, evaluated by a clinician with no significant rehabilitation contraindications, and able to participate in early rehabilitation activities; 5. Basic cognitive and communication abilities (e.g., Mini-Mental State Examination, MMSE score >= 17, or clinically judged to have the ability to understand and cooperate), able to participate in study assessments; 6. No history of serious neurological diseases or disabilities affecting functional status (such as long-term bedridden conditions not caused by the current stroke); 7. Has not received systematic rehabilitation behavioral interventions or participated in other interventional clinical studies before enrollment; 8. The patient or their legal representative provides informed consent and signs the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Age under 18 years old; 2. Stroke not confirmed through clinical and imaging (CT or MRI), or diagnosis unclear; 3. Not in the acute or early recovery stage of stroke (more than 14 days since onset), or not hospitalized; 4. Condition unstable or having rehabilitation contraindications, assessed by a physician as unsuitable for rehabilitation activities; 5. Significant cognitive or communication impairments (e.g., MMSE<17 or unable to understand instructions), unable to complete assessments or cooperate with interventions; 6. History of serious neurological diseases or functional impairments (e.g., long-term bedridden, severe disability not caused by the current stroke) that affect the evaluation of study outcomes; 7. Already received systematic rehabilitation behavioral interventions before enrollment or currently participating in other interventional studies; 8. Unable to provide informed consent (patient or legal representative does not agree to participate in the study).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rehabilitation Behavior Initiation Rate;Time to First Rehabilitation Behavior Initiation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Improvement in Functional Outcomes (Supportive Outcome);Incidence of Rehabilitation Behavior Interruption or Avoidance;Maintenance of Rehabilitation Behaviors (Frequency/Target Achievement Days); | — |
Countries
China
Contacts
Zhenjiang First People's Hospital