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Research on Time-Based Rehabilitation Strategies after Stroke

Research on Time-Based Rehabilitation Strategies after Stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125338
Enrollment
Unknown
Registered
2026-05-25
Start date
2026-05-30
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Stroke: sudden onset of contralateral limb numbness, weakness, sensory deficits, monocular vision loss, vertigo, diplopia, bilateral vision loss, ataxia, etc.

Interventions

PT1 group:Physical Therapy(PT)

Sponsors

Beijing Bo'ai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for ischemic stroke as defined by the "Chinese Guidelines for the Diagnosis of Major Cerebrovascular Diseases 2019", confirmed by cranial CT or MRI. 2. Aged 18 to 65 years, any gender. 3. First-ever stroke, with a disease duration of 1 to 6 months. 4. Unilateral hemiplegia, with Brunnstrom stage >= III. 5. No significant aphasia or cognitive impairment (MMSE >= 24). 6. No progression of neurological symptoms for more than 48 hours. 7. Signed informed consent form. 8. Ability to comply with all study procedures and participate in all treatments and assessments.

Exclusion criteria

Exclusion criteria: 1. Severe depression; 2. Comorbid with other severe neurological or psychiatric disorders (including but not limited to dementia, Parkinson's disease, or alcoholism); 3. Comorbid with severe medical conditions that persistently affect the patient's full participation in the study (including but not limited to advanced chronic obstructive pulmonary disease, hepatic or renal failure, advanced congestive heart failure, severe anemia, coagulation disorders, malignant tumors, etc.), with an expected survival of less than 6 months; 4. Comorbid with other diseases affecting the function of the affected limb (including but not limited to severe arthritis, Dupuytren's contracture, etc.); 5. Concurrent participation in another investigational therapeutic or interventional study, or participation in other similar clinical trials within the past three months.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment for Motor Function (FMA) Score;24-hour Heart Rate;128-channel Electroencephalography (128-channel EEG);

Secondary

MeasureTime frame
Pittsburgh Sleep Quality Index (PSQI);Modified Barthel Index (MBI);Fugl-Meyer Balance Scale (FMA-Balance) Score;Muscle Tone;Body Temperature;

Countries

China

Contacts

Public ContactTong Zhang

Beijing Bo'ai Hospital

Tom611@126.com+86 137 0139 5491

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026