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Efficacy of Follow-up Monitoring on Rehabilitation Status and Hand Function Recovery in Stroke Patients at 1 Year After Discharge (FOLLOW-STROKE-HAND)

Efficacy of Follow-up Monitoring on Rehabilitation Status and Hand Function Recovery in Stroke Patients at 1 Year After Discharge (FOLLOW-STROKE-HAND): Protocol for a Longitudinal Observational Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119007
Enrollment
Unknown
Registered
2026-02-13
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Stroke

Interventions

Multidisciplinary Collaborative Rehabilitation Group:Hospital-Community-Family Multidisciplinary Collaborative Rehabilitation Management

Sponsors

The Second People's Hospital of Hefei, Anhui Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meeting the diagnostic criteria for stroke, confirmed by cranial CT or MRI; 2. Aged 18-80 years; 3. The score of the Fugl-Meyer Assessment Scale for the affected hand (FMA-Hand) is = 20 points, and being able to cooperate with assessments and questionnaires; 5. Voluntarily signing the informed consent form; 6. Residing in Hefei City, with an expected survival time of >= 1 year, and being able to cooperate with 1-year follow-up and motor evoked potential (MEP) testing.

Exclusion criteria

Exclusion criteria: 1. Severe cognitive impairment, aphasia, or mental illness, making effective communication impossible; 2. A history of neurological diseases or severe osteoarthropathy that affects the assessment of hand function; 3. Complicated with severe dysfunction of major organs, malignant tumors, or severe infections; 4. Pregnant or lactating women; 5. Planning to move out of Hefei after discharge and unable to complete follow-up; 6. Participation in other similar rehabilitation studies within the past month; 7. Having contraindications to MEP testing (such as internal metal implants, history of epilepsy, etc.).

Design outcomes

Primary

MeasureTime frame
Hand Function;

Secondary

MeasureTime frame
Overall sports function;Activities of Daily Living (Modified Barthel Index);Complication Rate;Rehabilitation Satisfaction;

Countries

China

Contacts

Public ContactFangjun Xu

The Second People's Hospital of Hefei

1065519857@qq.com+86 187 8886 8897

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 29, 2026