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Application of Baduanjin Therapy in Early Rehabilitation of Noninvasive Ventilation Patients

Application of Baduanjin Therapy in Early Rehabilitation of Noninvasive Ventilation Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015011
Enrollment
Unknown
Registered
2018-02-28
Start date
2018-03-20
Completion date
Unknown
Last updated
2018-03-05

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

Conditions

Noninvasive ventilation patients

Interventions

Intervention group:Baduanjin Therapy + routine treatment
Control group:Routine treatment

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Early rehabilitation indicators refer to "2014 Active Mechanical Safety Standard for Severe Patients with Mechanical Ventilation" 1. patients responded to verbal stimuli [Richmond restless sedation score (RASS) -1 to +1], delirium assessment (CAM-ICU) normal; 2. Inhalation oxygen concentration (FiO2) <0.60; PEEP = 10 cmH2O; respiratory rate < 30 bpm; 3. muscle strength = 4 or more; 4. blood pressure did not receive support or low level of support above the lower limit of the target range; 5. stable autonomic heart rate or stable rapid arrhythmia <120 beats / min; Measures; No activity contraindications (such as unstable fractures).

Exclusion criteria

Exclusion criteria: 1. patients with mechanical ventilation, inhaled oxygen concentration = 0.6, PEEP = 12cmH2O; 2. the use of two vasoactive drugs; 3. active myocardial ischemia or cardiogenic shock, heart failure (grade III-IV) and malignant arrhythmia; 4. delirium obvious agitation; 5. poor compliance.

Design outcomes

Primary

MeasureTime frame
Mechanical ventilation time;ICU-AW;

Countries

China

Contacts

Public ContactXiaoxuan Zhang

Guangdong Provincial Hospital of Chinese Medicine

zhxiaoxuan2003@163.com+86 13922468632

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026