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Early curative effect of suspended lower limb rehabilitation robot in patients with Intensive Care Unit-acquired muscle weakness (FITonICU)

Early curative effect of suspended lower limb rehabilitation robot in patients with Intensive Care Unit-acquired muscle weakness (FITonICU)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070118
Enrollment
Unknown
Registered
2023-04-03
Start date
2023-04-03
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Intensive Care Unit-acquired muscle weakness (FITonICU)

Interventions

Control group:Routine rehabilitation training
MOTOmed lower limb Rehabilitation Trainer interventional group:MOTOmed lower limb rehabilitation trainer assisted treatment
Suspended lower limb rehabilitation robot intervention group:Assisted treatment by a suspended lower limb rehabilitation robot

Sponsors

Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Primary critical disease, meeting the diagnostic criteria for ICU acquired myasthenia; (2) The patient was hospitalized in ICU for 2 weeks with mechanical ventilation for more than 48 hours; (3) Aged 18-85; (4) lower extremity motor dysfunction; (5) Clear consciousness, good cardiopulmonary function, stable vital signs, able to cooperate well with training; (6) Promise to abide by the research procedures, cooperate with the whole process of the study and sign the informed consent; (7) Commit to follow the lifestyle considerations during the study.

Exclusion criteria

Exclusion criteria: (1) Lack of informed consent; (2) Patients with implanted pacemaker or defibrillator; (3) patients with unhealed fractures, severe osteoporosis and acute venous thrombosis; (4) Patients with severe hypertension (systolic blood pressure >200mmHg, diastolic blood pressure >110mmHg), diabetes with poor blood sugar control or complicated with serious diseases such as dysfunction of liver, kidney, heart and other important organs; (5) severe limited passive range of motion of hip, knee and ankle joints; (6) Refractory or multiple epilepsy; (7) severely impaired in vision, hearing or understanding; (8) participating in another clinical trial; (9) Known to have allergic reaction, hypersensitivity or intolerance to rehabilitation robots; (10) Any condition which, in the opinion of the investigator, is likely to prejudice the subject or cause the subject to fail to meet or perform the study requirements.

Design outcomes

Primary

MeasureTime frame
Muscle thickness of key muscles of lower limbs;

Secondary

MeasureTime frame
medical research council,MRC;modified barthel index,MBI;Measurement of lower limb circumference;

Countries

China

Contacts

Public ContactFanfu Fang

Shanghai Changhai Hospital

fangfanfu@126.com15800719913

Outcome results

None listed

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