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STEPS To ICU Recovery

Body weight-supported treadmill training for patients in the intensive care unit: a multicentre randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20691
Enrollment
88
Registered
2017-12-01
Start date
2017-12-08
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

Critical illness, early mobilisation, intensive care, ICU-aquired weakness, ambulation.

Interventions

Particlpants who are randomized into the lntervention group will receive BWSTT in addition to usual care. The BWSST intervention consists of walking on a treadmill while supported by a hamess. The int

Sponsors

Academic Medical Center Amsterdam (AMC]
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Admission at ICU for medica! or surgical reasons, age 2:18, Mechanica! ventilatlon 2:48 hours, Meeting safety critiria vor rehabilitation according to the Evidence Statement for ICU physiotherapy (Sommers, 2016)

Exclusion criteria

Exclusion criteria: Not meeting the safety criteria for rehabilitation according to the evidence statement for ICU physiotherapy. Imminent to death. Insufficient knowledge of the Dutch language. Unable to walk in the month prior to ICU admission. Neurological diseases and disorders as reason for ICU admission. One or more amputated lower extremities. Mental retardation

Design outcomes

Primary

MeasureTime frame
The primary objective is to investigate the effect of BWSTT in critically ill patients on time to functional ambulation

Secondary

MeasureTime frame
The secondary objectives of this study are to investigate the effects on other patient relevant outcome measures for the evaluation of BWSTT. These outcomes are walking capacity, walking distance, muscle strength, ICU acquired weakness, symptoms of post-traumatic stress, experienced exertion after physiotherapy (PT) intervention, training intensity (i.e. respiratory frequency, heart rate, blood pressure and oxygen saturation) of PT interventions, status of functional independency, functional ambulation, duration of mechanical ventilation, (Serious) Adverse Events), number of staff needed, time spent on intervention and patient satisfaction.

Contacts

Public ContactMarike van der Schaaf

Postbus 22660

m.vanderschaaf@amc.uva.nl020-5664421

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)