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The clinical effectiveness of kinesio taping combined with early rehabilitation training in patients with acute respiratory failure requiring mechanical ventilation.

The clinical effectiveness of kinesio taping combined with early rehabilitation training in patients with acute respiratory failure requiring mechanical ventilation.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095207
Enrollment
Unknown
Registered
2025-01-03
Start date
2025-01-10
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

None

Interventions

Experimental group:Kinesio tape paste
Placebo group:Non-elastic tape paste

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. All meet the diagnostic criteria for acute respiratory failure,and are caused by acute respiratory failure due to respiratory system diseases such as COPD. 2. Age between 18-80 years; 3. Mechanical ventilation time=10 points; 7. Other systems such as circulatory,neurological,and surgical are stable:the patient responds to sound,RASS score>-3,PaO2>80 mmHg,PEEP90%,stable blood pressure,hemodynamic stability,no arrhythmias,no myocardial ischemia; 8. Signed informed consent;

Exclusion criteria

Exclusion criteria: 1. Those who do not meet the above inclusion criteria; 2. Pregnant or lactating; 3. Allergic to adhesive materials (acrylic acid, etc.); 4. Skin disorders, such as acute neurodermatitis or psoriasis; 5. There was a tendency of tension blisters before application; 6. Combined with primary diseases affecting muscle strength, such as cerebrovascular disease, spinal cord injury, myasthenia gravis, etc. 7. Color Doppler ultrasound showed pleural effusion, pneumothorax, pleural adhesion, etc. 8. Abdominal hypertension syndrome or rib disease (such as rib fracture, rib metastasis, etc.); 9. Active bleeding; 10. Use of muscle relaxants within 24 hours before enrollment.

Design outcomes

Primary

MeasureTime frame
Mechanical ventilation time;Diaphragmatic motion;Incidence of ICU-AW;Offline success rate;Hospitalization days;

Secondary

MeasureTime frame
Quality of life;Incidence of ventilator-associated pneumonia;Safety indicators;Activities and participants;Incidence of atelectasis;compliance indicators;

Countries

China

Contacts

Public ContactZhou Ruijuan

Shanghai General Hospital

zrj1008@126.com+86 18721787291

Outcome results

None listed

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