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Aerobic training for hemiparetic ischaemic stroke patients in acute phase – a randomized controlled trial

Aerobic training for hemiparetic ischaemic stroke patients in acute phase – study protocol for a randomized controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031379
Enrollment
Unknown
Registered
2020-03-29
Start date
2020-04-20
Completion date
Unknown
Last updated
2020-03-30

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

Conditions

stroke

Interventions

B:aerobic exercise with usual care

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 80 years; 2. Diagnosis of stroke within 24h after stroke as ischaemic stroke determined by initial MRI/CT scan of the brain; 3. Unilateral hemispheric stroke, with both upper- and lower- motor deficiency assessed by National Institutes of Health Stroke Scale (NIHSS), scored >=3; 4. Medical stable, and considered able to perform aerobic exercise, as determined by physicians. Systolic blood pressure (SBP) between 110 mmHg and lower than 200mmHg, Diastolic blood pressure (DBP) between 40 mmHg and lower than 110mmHg, oxygen saturation > 92% with oxygen supplementation, resting heart rate between 40 beats per minute and 110 beats per min, temperature less than 38 degree C; 5. Able to provide consent to take part in the study and to comply with the requirements of the protocol.

Exclusion criteria

Exclusion criteria: 1. Stroke of intracranial haemorrhage primarily due to bleeding; 2. Unstable medical history, or unstable cardiological condition (e.g., myocardial infarction, atrial fibrillation), which might impose danger for patients during exercise; 3. Severe heart disease which may endanger the patients while doing exercise; 4. repeated stroke (more than 3 times); 5. Cognition impairment unable to understand the instructions of physiotherapist for exercise training; 6. Pre-morbid modified Rankin Scale (mRS) >3, or both limbs are unable to perform exercise voluntarily; 7. Involved in other studies.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer assessment;walking time in 10 meters;

Secondary

MeasureTime frame
Self-care ability;walking distance in 6 minutes;Berg balance scale;

Contacts

Public ContactJie Jia

Huashan Hospital, Fudan University

shannonjj@126.com+86 13611722357

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026