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A study on the Impact of increased lower extremity Training on the Coughing ability of Patients with tracheotomy

Clinical study on the influence of active and passive lower extremity training devices on the coughing ability of patients undergoing tracheotomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106238
Enrollment
Unknown
Registered
2025-07-21
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-08-18

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 lower 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 lower 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. Patients with stroke (ischemic or hemorrhagic) or brain trauma that meet clinical diagnostic criteria; 2. First onset, within 3 months of disease course; 3. Adult patients with tracheotomy (tracheostomy) (aged 18-70 years); 4. Muscle tone score (MAS score) below grade 2; 5. GCS > 8 and able to follow three-step instructions; 6. Stable vital signs; 7. Signed informed consent form (legal representative).

Exclusion criteria

Exclusion criteria: 1. Complications such as severe heart, liver or kidney dysfunction, uncontrolled severe hypertension or diabetes, or other unstable internal diseases may significantly affect the safety, tolerance or cause confusion regarding the reasons for muscle changes; 2. Other clear and independent causes of muscle atrophy exist, including myasthenia gravis, muscular dystrophy, motor neuron disease, recent fractures or orthopedic surgeries affecting the lower limbs; 3. Special treatments that may significantly affect muscle mass have been received within 1 month prior to the start of the study; 4. Other circumstances that make one ineligible to participate in the trial.

Design outcomes

Secondary

MeasureTime frame
Modified Barthel Index;Cough peak flow value;Manual muscle test;

Primary

MeasureTime frame
Muscle thickness and mass were measured by ultrasound;Lung function;

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: Feb 4, 2026