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Early mobilization for patients with noninvasive positive pressure ventilation in Intensive Care Unit:A randomized controlled trial

Early mobilization for patients with noninvasive positive pressure ventilation in Intensive Care Unit:A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021797
Enrollment
Unknown
Registered
2019-03-10
Start date
2018-04-01
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

ICU-acquired weakness

Interventions

Experimental group:Early mobilization and routine nursing of ICU
control group:routine nursing of ICU

Sponsors

School of Stomatology, Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Patients'aged 18 years or above; (2) Intensive care unit patients with non-invasive positive pressure ventilation; (3) Using non-invasive positive pressure ventilation for 24 hours or longer; (4) Patients being ware and responsible to researcher's directions; (5) Voluntary participate in the study.

Exclusion criteria

Exclusion criteria: (1) Glasgow Coma Score 12 or lower; (2) Patients being unable to create any movements; (3) Previously non-invasive mechanical ventilation treatments outside ICU for 48 hours or longer; (4) Patients with irreversible diseases and six-month mortality being 50% or higher; (5) Patients who had machanically ventilation before; (6) Consistent failure to meet the requirements of early mobilization; (7) Patients with sereve infectious diseases.

Design outcomes

Primary

MeasureTime frame
The incidence rate of ICU-acquired weakness;MRC-score;the length of stay in ICU;duration of noninvasive ventilation;

Secondary

MeasureTime frame
grip strength;

Countries

China

Contacts

Public ContactYanhao Wang

College of Stomatology, Chongqing Medical University

wyh1572343@163.com+86 15723433022

Outcome results

None listed

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