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Recruiting Not applicable

Effectiveness of Early Intervention With Virtual Reality-Based Interactive Rehabilitation on Upper Extremity Muscle Strength, Cognitive Status, Hospital Anxiety, and Exercise Self-Efficacy in Patients With Acute Ischemic Stroke

NCT07674329 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2025-03-07
Last updated
2026-06-29

Condition(s) studied

Acute Ischemic Stroke

Investigational drug(s) / intervention(s)

Virtual reality-based interactive rehabilitationbedside rehabilitation

Virtual reality-based interactive rehabilitation: Virtual reality

bedside rehabilitation: traditional bedside rehabilitation

Study summary

This interventional study evaluates the impact of early virtual rehabilitation, starting 24 hours post-diagnosis of acute ischemic stroke, on upper limb strength, cognitive status, and self-efficacy. The goal is to establish more effective rehabilitation protocols for acute ischemic stroke patients and to boost their motivation to participate in training.

Eligibility

Sex
ALL
Min age
18 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosis of acute ischemic stroke with ICD-10 codes: G45-G46.8, I63-I68.8. * Within 10 days (inclusive) of stroke symptom onset. * Age 18\~85 years or older. Exclusion Criteria: * Comorbid neuromuscular or orthopedic conditions affecting upper limb function.) * Recurrence of stroke or onset of seizures during the study period. * Severe visual impairment or visuospatial neglect. * Inability to cooperate or refusal to participate in the study.

Primary outcome measure(s)

  • upper limbs function — 7days later
    FMA-UE
  • cognitive status — 7days later
    SLUME

Trial sites (1)

FacilityCityRegionStatus
Tri Service General Hospital Taipei Taiwan Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07674329 on ClinicalTrials.gov ↗ ← All trials in Taiwan