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The Effect of Very Early Bedside Cycle Exercise on ICU-acquired Weakness

The Effect of Very Early Bedside Cycle Exercise on ICU-acquired Weakness

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900020960
Enrollment
Unknown
Registered
2019-01-23
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

ICU-acquired weakness

Interventions

Group 1:very early bedside cycle exercise
Group 2:early bedside cycle exercise

Sponsors

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. When entering the ICU<24h; 2. The estimated mechanical ventilation time is =48h; 3. When entering the ICU, the RASS sedation assessment score is between -2 and -5; 4. Aged 18 to 80 years; 5. Weight <135 kg (maximum weight of bedside bicycle); 6. Voluntary participants after communicating with the patient's family members; 7. No brain organic lesions; 8. The patient's circulation was stable within 24 hours of ICU, with or without vasoactive drugs to maintain the target blood pressure for at least 2 hours, and the vasoactive drug dose was unchanged; 9. The patient's breathing was stable within 24 hours of ICU, respiratory rate 5-40 beats / min, SPO2=90%; Patients with mechanical ventilation had FiO2=0.6 and PEEP =10cmH2O.

Exclusion criteria

Exclusion criteria: 1. Have primary motor dysfunction or clear neuromuscular diseases, such as myasthenia gravis, Guillain-Barre syndrome, amyotrophic lateral sclerosis, etc.; 2. Lumbar vertebrae, pelvis, lower extremity trauma or surgery; 3. Increased intracranial pressure; 4. Limb defects; 5. Lower extremity arterial catheterization, continuous acceptance of CRRT, IBAP, ECMO; 6. Deep vein thrombosis of the lower extremities; 7. There is active bleeding 8. Having a pacemaker or an implantable defibrillator; 9. Pregnant women; 10. Redness, bleeding, etc. occurred in the measurement points of the lower extremities; 11. Expecting death or performing palliative care; 12. Participate in other research.

Design outcomes

Primary

MeasureTime frame
Muscle strength;

Secondary

MeasureTime frame
muscle mass;

Countries

China

Contacts

Public ContactLong Yun
tjmuhhw@163.com+86 13421376044

Outcome results

None listed

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