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Evaluation of the sensitivity of the upper limb trunk muscle groups to training in long-term bedridden patients after stroke and brain trauma

Evaluation of upper limb trunk muscle groups in patients who have been bedridden for a long time after stroke and brain trauma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104415
Enrollment
Unknown
Registered
2025-06-17
Start date
2025-06-20
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Stroke, Brain injury

Interventions

Intervention group A:After 7 days of regular rehabilitation combined with additional active and passive upper limb training, 7 days of regular rehabilitation training will be conducted
Intervention group B:After 7 days of regular rehabilitation training, 7 days of regular rehabilitation combined with additional active and passive upper limb training were carried out

Sponsors

The Second Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Clinical diagnosis of ischemic or hemorrhagic stroke, or moderate-severe traumatic brain injury (GCS initial score <=12); 2. The first onset of the disease, the course of the disease is within 3 months; 3. Muscle loss (MMT<=4) due to neurological deficits (hemiplegia/quadriplegia, balance disorders, consciousness disorders, etc.), which is regarded as the need for long-term bed rest; 4. Stable vital signs;

Exclusion criteria

Exclusion criteria: 1. Combined with severe cardiopulmonary diseases (such as NYHA cardiac function grade III-IV, COPD GOLD grade 3-4), severe liver and kidney insufficiency, active malignant tumors; 2. Fractures, severe arthritis, infections, skin breakdowns, etc., in the upper limbs or trunk that affect the assessment or training; 3. Previous history of neuromuscular diseases affecting upper limb function (such as muscular dystrophy, motor neuron disease); 4. Severe mental illness and inability to cooperate with assessment and training; 5. Presence of severe spasticity (modified Ashworth scale >=grade 3) or contractures, with significant limitation of passive activities; 6. Planned surgical or medication modification that may significantly affect muscle status during the study period.

Design outcomes

Primary

MeasureTime frame
Muscle thickness and mass were measured by ultrasound;Cough peak flow value;

Secondary

MeasureTime frame
Modified Barthel Index;

Countries

China

Contacts

Public ContactLihua Jin

The Second Affiliated Hospital of Kunming Medical University

kimlihua109@naver.com+86 871 6340 2692

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 1, 2026