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A Study on the Safety and Effectiveness of Early Cardiorespiratory Fitness Training in Patients with Acute Ischemic Stroke

A Study on the Safety and Effectiveness of Early Cardiorespiratory Fitness Training in Patients with Acute Ischemic Stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113233
Enrollment
Unknown
Registered
2025-11-26
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Acute Ischemic Stroke,AIS

Interventions

intervention group:Conventional rehabilitation therapy + 30-minute CRF training
control group:Conventional rehabilitation therapy + 30-minute rehabilitation education session?

Sponsors

Jing'an District Central Hospital of Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.? Meet the diagnostic criteria outlined in the Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2023; 2.? Presence of cerebral infarction confirmed by CT or MRI, with a definitive diagnosis of ischemic stroke; 3.? Time since the current onset is =2; 6.? The muscle strength of the non-hemiplegic limb, assessed by Manual Muscle Testing (MMT), is >= grade 3; 7.? Possess normal communication and expression abilities, enabling effective interaction with healthcare staff and adherence to rehabilitation therapy instructions; 8.? Have stable vital signs and are free of severe complications; 9.? The subject themselves or their family members are fully informed about the study details and have provided signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Hemorrhagic transformation or large-area cerebral infarction with unstable clinical condition; 2. Severe cardiovascular diseases: e.g., unstable angina, acute myocardial infarction, heart failure, severe arrhythmia, or uncontrolled hypertension (>180/110 mmHg); 3. Severe psychiatric disorders, cognitive impairment, or language dysfunction that would impede compliance with rehabilitation therapy; 4. Presence of severe pain or spasticity symptoms; 5. Patients unable to cooperate with assessments or with poor adherence; 6. Patients who developed severe adverse reactions or clinical deterioration after thrombolysis or thrombectomy.

Design outcomes

Primary

MeasureTime frame
Rate of Perceived Exertion, RPE;Fugl-Meyer Assessment, FMA ;

Secondary

MeasureTime frame
Short Physical Performance Battery, SPPB;chest expansion;2-minute step test, 2MST;Pulmonary Function Test Parameters;Oxygen Saturation(SpO2), Blood Pressure(BP), Heart Rate(HR), Respiration, Body Temperature;Modified Barthel Index,MBI;Generalized Anxiety Disorde-7, GAD-7;Berg Balance Scale, BBS;Grip strength, pinch strength, upper arm flexion and extension circumference, thigh circumference, waist circumference, hip circumference;Patient Health Questionnaire-15,PHQ-15;Patient health questionnaire-9,PHQ-9;

Countries

China

Contacts

Public ContactCheng Bingyuan

Jing'an District Central Hospital of Shanghai

363868852@qq.com+86 21 6157 8072

Outcome results

None listed

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