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Early mobilization in the Intensive and Medium care unit by the use of mobile monitoring: a single center randomized trial

Early mobilization in the Intensive and Medium care unit by the use of mobile monitoring: a single center randomized trial - EARLY-MOB trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON53218
Enrollment
82
Registered
2023-05-31
Start date
2023-10-29
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

early mobilization ICU rehabilitation stage

Interventions

The intervention means monitoring with telemetry until discharge to the ward. The control group maintains conventional bedside monitoring until discharge to the ward.

Sponsors

St. Antonius Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • >=18 years • Minimum ICU/MCU stay 5 days • No expected discharge to the ward without continuous monitoring vital signs within 48 hours • Meets pre-defined criteria: o Hemodynamic stability o No use of inotropes/vasopressors o Not external pacemaker dependent o No significant cardiac arrhythmia or intervention in the last 48 hours • No arterial pressure catheter/line • Signed informed consent

Exclusion criteria

Exclusion criteria: - CVA during hospital admission, with limited mobility (hemiparesis) - Paraplegia due to myelum ischemia after aortic surgery - Guillain-Barre - Prescribed bed rest (e.g. type B dissection) - No signed informed consent - Not instructable or limited mobility - Patient has already been included in the study during hospital admission

Design outcomes

Primary

MeasureTime frame
Primary Goal: - Early mobilization measured by DEMMI score (within 24-48 hours after inclusion of the study and then twice a week by physiotherapist) - Muscle strength measured by MRC-SUM (within 24-48 hours after inclusion of the study and then twice a week by physiotherapist)

Secondary

MeasureTime frame
- Reducing anxiety and depression measured by HADS score at the time of inclusion of the study and in the first hours after discharge to the ward. - Feeling more safe measured by one question at the time of inclusion of the study and in the first hours after discharge to the ward.

Countries

Netherlands

Contacts

Public ContactI Pol

St. Antonius Ziekenhuis

i.van.de.pol@antoniusziekenhuis.nl0883206614

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Feb 3, 2026