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Increased Mobilization Frequency Pilot Trial Pilot study on the feasibility and effects of an increased mobilisation frequency in neurological Early Rehabilitation

Increased Mobilization Frequency Pilot Trial Pilot study on the feasibility and effects of an increased mobilisation frequency in neurological Early Rehabilitation - IMob Pilot

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00023235
Enrollment
20
Registered
2021-01-12
Start date
2021-01-26
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

I60-I69

Interventions

Group 1: Patients in the intervention group should be mobilized at least ten times per week, i.e. twice as often as the control group. The mobilizations will be performed as usual by physiotherapists,

Sponsors

Schön Klinik München Schwabing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patients in phase B early rehabilitation with subacute to chronic stroke (from ten days) with modified Rankin Scale 4-5 of 6. Craniotomized patients and patients with tracheal cannulas.

Exclusion criteria

Exclusion criteria: Lack of cardiopulmonary exercise capacity, autonomic vascular regulation failure and other circumstances that prevent regular mobilization to sitting and standing positions. Contraindications of mobilization, such as decubitus >2°, fractures, myocardial infarction, pulmonary embolism, ossifications, fresh decubitus cover. Persons over 90 and under 18 years.

Design outcomes

Primary

MeasureTime frame
Score on the STREAM (Stroke Rehabilitation Assessment of Movement) to measure motor function and balance. The assessment is performed for the first time after enrollment in the study and for the second time after the end of the four weeks of study participation.

Secondary

MeasureTime frame
Measurement of vigilance using the Glasgow Coma Scale. Speech production in patients with tracheal cannula is assigned as a pseudo score with a value of 1, 3 or 5. The assessment is conducted at the same time as the STREAM Assessment, the first time after enrollment in the study and the second time after the end of the four weeks of study participation.

Countries

Germany

Contacts

Public ContactFelix von Eichborn

Schön Klinik München Schwabing

mobilisationsstudie.schwabing@gmail.com089 360870

Outcome results

None listed

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