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Clinical application of warming regulating hand function therapeutic apparatus in rehabilitation treatment of post-stroke hand dysfunction

Clinical application of warming regulating hand function therapeutic apparatus in rehabilitation treatment of post-stroke hand dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000003589
Enrollment
Unknown
Registered
2020-08-17
Start date
2020-11-02
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

post-stroke hand dysfunction

Interventions

Sponsors

Beijing Xiaotangshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patients with 40-80 years old and accorded with the diagnosis of cerebrovascular disease; 2. All patients diagnosis confirmed by CT or MRI scan; 3. Patients with the first onset of disease or previous stroke history but without sequelae; 4. Those with clear consciousness and stable vital signs who cooperate with treatment; 5. Upper limb muscle strength >= grade 2, muscle tension <= grade 2 (modified Ashworth Spasticity scale (MAS)); 6. Patients who will only be received routine medication treatment and rehabilitation treatment after stroke during the trial, but did not take antispasmodic drugs before treatment; and 7. Voluntarily participated in the study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. The disease is in an advanced stage, Patients with severe infection and liver, heart, kidney and hematopoiesis system diseases; 2. Malignant progressive hypertension; 3. Severe diabetes mellitus; patients with skin damage that are difficult to recover; 4. Patients with previous motor dysfunction; 5. Patients with severe primary diseases and mental disorders; 6. Patients with agnosia, apraxia, aphasia, visual field and intelligence disorders; and 7. Patients who are unwilling to cooperate and have poor compliance.

Design outcomes

Secondary

MeasureTime frame
Rapid muscle measurement;Modifed Barthel index, MBI;Somatosensory evoked potential;Motor evoked potential;Modified Ashworth Scale, MAS;

Primary

MeasureTime frame
Fugl-Meyer Assessment Upper Extremeties;

Countries

China

Contacts

Public ContactSun Jie

Beijing Xiaotangshan Hospital

bingxuehaitun520@163.com+86 13488665637

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026