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Increasing Home-based Structured Physical Exercise After Ischemic Stroke: a Randomized Controlled, Open-label, Blinded Endpoint Trial

Increasing Home-based Structured Physical Exercise After Ischemic Stroke: a Randomized Controlled, Open-label, Blinded Endpoint Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112010
Enrollment
Unknown
Registered
2025-11-10
Start date
2025-11-11
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Ischemic Stroke

Interventions

Exercise intervention group:Subjects will undergo 4 weeks of home-based structured physical exercise guidance.
Control group:Subjects will not receive structured physical exercise guidance but are encouraged to engage in regular physical exercise.

Sponsors

Beijing Institute of Brain Disorders
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18 to 80; 2. Ischemic stroke onset within 1 year; 3. modified Rankin scale (mRS) score <= 3; 4. Signed informed consent from the patients or the legally authorized representatives.

Exclusion criteria

Exclusion criteria: 1. Stroke progression within the past 3 days (defined as an increase in NIHSS score of >= 4 points or an increase in any single item of >= 2 points); 2. Concurrent osteoarthritis, fractures, deep vein thrombosis, unstable angina, respiratory diseases, or amputation that may theoretically make it difficult for participants to complete the physical exercise; 3. Concurrent movement disorders such as Parkinson's disease or Parkinsonism; 4. Patients who have engaged in regular aerobic physical activity within the past 6 months, defined as more than 150 minutes of moderate-intensity aerobic physical activity; or more than 75 minutes of vigorous-intensity aerobic physical activity; or an equivalent combination of moderate- and vigorous-intensity activity throughout the week; 5. Unable to comply with the study procedures or follow-up due to psychiatric, cognitive, or emotional disorders; 6. Known pregnancy or lactation, or a positive pregnancy test; 7. Currently participating in another drug or device study; 8. Life expectancy less than 1 year; 9. Unable to communicate using a smartphone; 10. Other conditions considered by investigators to be unsuitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Total aerobic physical exercise time at week 4;

Secondary

MeasureTime frame
Moderate-intensity aerobic exercise time at week 4;Vigorous-intensity aerobic exercise time at week 4;International Physical Activity Questionnaire Short Form (IPAQ-SF) score at week 4;Exercise Adherence Rating Scale (EARS) Section B score at week 4;modified Rankin Scale (mRS) score at week 4;Resting heart rate at week 4;Resting blood pressure at week 4;

Countries

China

Contacts

Public ContactChuanjie Wu

Beijing Institute of Brain Disorders

wuchuanjie@ccmu.edu.cn+86 10 8319 9439

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026