Stroke
Conditions
Interventions
Intervention Group 1:Non-weight-bearing Test – Washout Period – Affected Side Weight-bearing Test – Washout Period – Unaffected Side Weight-bearing Test – Washout Period – Trunk Weight-bearing Test –
Intervention Group 2:Non-weight-bearing Test – Washout Period – Affected Ankle and Contralateral Lumbar Weight-bearing Test – Washout Period – Trunk Weight-bearing Test – Washout Period – Unaffected A
Intervention Group 3:Affected Ankle and Contralateral Lumbar Weight-bearing Test – Washout Period – Non-weight-bearing Test – Washout Period – Affected Ankle Weight-bearing Test – Washout Period – Una
Intervention Group 4:Unaffected Ankle Weight-bearing Test – Washout Period – Affected Ankle Weight-bearing Test – Washout Period – Non-weight-bearing Test – Washout Period – Affected Ankle and Contral
Intervention Group 5:Unaffected Ankle Weight-bearing Test – Washout Period – Trunk Weight-bearing Test – Washout Period – Affected Ankle and Contralateral Lumbar Weight-bearing Test – Washout Period –
Sponsors
Shaanxi Rehabilitation Hospital
Eligibility
Sex/Gender
All
Age
40 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Meets the diagnostic criteria for stroke established by the National Cerebrovascular Disease Conference, with confirmation by CT or MRI. 2. First stroke onset, with a disease duration between 3 months and 2 years. 3. Unilateral hemiplegia. 4. Holden Functional Ambulation Classification >= level 2, able to walk independently without assistance for at least 10 meters. 5. Mini-Mental State Examination score >= 24 points, capable of understanding and following instructions. 6. Voluntarily participates and provides written informed consent.
Exclusion criteria
Exclusion criteria: 1. Presence of other neurological or musculoskeletal disorders that significantly affect walking function. 2. Severe dysfunction of vital organs (e.g., heart, lung, liver, or kidney). 3. Severe spasticity on the affected lower limb (Modified Ashworth Scale score > 2) or limited joint range of motion. 4. Severe visual or vestibular impairment affecting balance. 5. Participation in other clinical trials that may influence walking function.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Peak Moment Asymmetry Ratio of the Hip Joint (Unaffected vs. Affected Side) During Stance Phase;Peak Moment Asymmetry Ratio of the Knee Joint (Unaffected vs. Affected Side) During Stance Phase;Peak Moment Asymmetry Ratio of the Ankle Joint (Unaffected vs. Affected Side) During Stance Phase; | — |
Secondary
| Measure | Time frame |
|---|---|
| Step Length Asymmetry Ratio;Single-Limb Support Time Asymmetry Ratio;Sagittal Plane Range of Motion Asymmetry Ratio of the Hip Joint;Sagittal Plane Range of Motion Asymmetry Ratio of the Knee Joint;Sagittal Plane Range of Motion Asymmetry Ratio of the Ankle Joint;Overall Walking Speed and Cadence; | — |
Countries
China
Contacts
Public ContactChen Longwei
Shaanxi Rehabilitation Hospital
Outcome results
None listed