Robotic-assisted early mobilization on the intensive care unit

Robotic-assisted early mobilization on the intensive care unit - ROBI-Trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00030062

Enrollment

Registered

2022-10-21

Start date

2022-10-24

Completion date

Unknown

Last updated

2025-10-06

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

Conditions

I60-I69 G62.80 G72.80 S06 G93 G82 G93 G61

Interventions

Group 1: Intervention group: nurses mobilise the study participants using the robotic device VEMOTION Group 2: Control group: nurses mobilise the study participants without using the robotic device VE

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: All patients admitted to the intensive care unit of the Schön Klinik Bad Aibling

Exclusion criteria

Exclusion criteria: - Emergency admission from the neurological or orthopedical department of the Schön Klinik Bad Aibling - Contraindications for mobilisation (decision is taken by the the attending intensive care physician) - renal dialysis requirement on admission

Design outcomes

Primary

Measure	Time frame
Time spent mobilising the study participants measured by activePAL sensors	—

Secondary

Measure	Time frame
Days without ventilation, days without special intensive care needs, mortality, time needed to complete the weaning process, complications due to mobilisation therapy, number of therapy interruptions while mobilising the patient,functional status at discharge using Functional Status Score on ICU (FSS-ICU), cognitive status and delirium using Confusion Assessment Method for ICU (CAM-ICU), patient satisfaction with the mobilisation therapy, nurses workload (NASA-TLX)	—

Measure

Time frame

Days without ventilation, days without special intensive care needs, mortality, time needed to complete the weaning process, complications due to mobilisation therapy, number of therapy interruptions while mobilising the patient,functional status at discharge using Functional Status Score on ICU (FSS-ICU), cognitive status and delirium using Confusion Assessment Method for ICU (CAM-ICU), patient satisfaction with the mobilisation therapy, nurses workload (NASA-TLX)

—

Countries

Germany

Contacts

Public ContactAlisa Buetikofer

Schön Klinik Bad Aibling Harthausen

ABuetikofer@schoen-klinik.de08061 / 903 - 1948

Outcome results

None listed

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