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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

ConditionAcute Ischemic Stroke
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-85
SponsorTri-Service General Hospital (TSGH)

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

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.

Disqualifiers

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.

Trial design

Design model

Sequential

Treatments tested in this trial

  • Virtual reality-based interactive rehabilitation

    Device

    Virtual reality

  • bedside rehabilitation

    Behavioral

    traditional bedside rehabilitation

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Early intervention in patients with acute ischemic strokeExperimental treatment 1 intervention
Group B: traditional rehabilitation.Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

upper limbs function

FMA-UE

Time frame
7days later
2

cognitive status

SLUME

Time frame
7days later

Secondary outcomes

1

Change in Self-Efficacy for Exercise (SEE) Scale Score

Self-efficacy will be assessed using the Self-Efficacy for Exercise (SEE) Scale. The SEE is a 10-item questionnaire that evaluates participants' confidence in their ability to continue exercising under various circumstances. Total scores range from 10 to 40, with higher scores indicating greater exercise self-efficacy.

Time frame
Baseline and 7 days after intervention

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Tri-Service General Hospital (TSGH)

Lead sponsor

Source ClinicalTrials.gov
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