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Implementation of Digital Integrated Solutions in Stroke Rehabilitation

Applied Research on Integrated Stroke Rehabilitation System Development with AI Assistance

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109069
Enrollment
Unknown
Registered
2025-09-11
Start date
2025-10-31
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

First-episode stroke patients

Interventions

Intervention: Smart Rehabilitation Management Program:Intervention: Smart Rehabilitation Management Program
Control Group (Rehabilitation-as-usual):Conventional Rehabilitation Intervention Model

Sponsors

The First Affiliated Hospital of Xinxiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria will be established based on disease diagnosis: 1. Diagnosis: Confirmed ischemic/hemorrhagic stroke (>=48 hours post-onset) meeting both CT/MRI diagnostic criteria and the 2019 Stroke Diagnostic Guidelines; 2.Motor Function: Fugl-Meyer Assessment (FMA) score <85 (upper or lower extremity); 3.Activities of Daily Living (ADL): Barthel Index (BI) score <=60; 4. Demographics: Age 18–80 years, with capacity to provide informed consent (or via legally authorized representative); 5. Clinical Stability: Hemodynamically stable with medication-controlled blood pressure <180/100 mmHg;

Exclusion criteria

Exclusion criteria: 1. Active malignancy or life expectancy <1 year; 2.Severe cognitive impairment (MMSE <10 or inability to comply with assessments) ; 3. Implanted electronic medical devices (e.g., cardiac pacemakers, deep brain stimulators) ; 4. Previous rehabilitation therapy for the same condition (potential interference with outcome evaluation) Special Populations; 5. Pregnancy or lactation; 6. Concurrent participation in other interventional rehabilitation trials ; 7. Inability to use smart devices (digital literacy requirement) ; 8. Other contraindications per investigator’s discretion;

Design outcomes

Primary

MeasureTime frame
Rehabilitation Intervention Rate;Rehabilitation expenditure as a percentage of total medical spending;Utilization Rate of Rehabilitation Resources;Efficiency of Rehabilitation Evaluation;

Secondary

MeasureTime frame
Inpatient Stay Duration (days);Total hospitalization costs (?);Adverse Event Incidence Rate;Satisfaction Assessment;

Countries

China

Contacts

Public ContactWang Yuchang

The First Affiliated Hospital of Xinxiang Medical University

yuchangrehab@163.com+86 187 9066 2962

Outcome results

None listed

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