Bedside medical training therapy in the acute rehabilitation setting - a pilot study

Bedside medical training therapy in the acute rehabilitation setting - a pilot study - Bedside-MTT

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00032401

Enrollment

Registered

2023-07-28

Start date

2023-08-29

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

Immobility

Interventions

Group 1: Bedside MTT (medical training therapy) as add-on to acute (in-hospital) rehabilitation complex therapy Group 2: Acute (in-hospital) rehabilitation complex therapy

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Interdisciplinary early rehabilitation immobility (CHARMI < 5) sufficient understanding of speech basic physical ability for MTT available consent

Exclusion criteria

Exclusion criteria: Delir Exceeding the maximum dimensions for the use of the therapy system (foot/US too large for the foot shells, 200 cm, > 180 kg) Bone instability (partial load UEx postoperatively, osteoporosis, osteogenesis imperfecta) Acute inflammation (e.g. of the joints) Acute thrombosis Fresh neurological deficits Acute herniated disc Pre-damaged tendons (risk of rupture) ROM restriction UEx Severe contractures or fixed spasticity with hip and knee flexion or extension deficit > 30 °. Open body parts in contact with the device Expected incompliance (assessment of the study physician) Existing absolute or relative contraindications to bemo therapy Expected study drop out

Design outcomes

Primary

Measure	Time frame
The purpose of the study is to assess feasibility and safety as well as system usability on the part of patients and therapists. In addition, exploratory data on clinical outcomes will be used to generate endpoints for a subsequent confirmatory randomized controlled trial.	—

Secondary

Measure	Time frame
- Safety (MTT-associated complication rate) - Feasibility (user survey) - Usability from the perspective of the physiotherapist - Usability from patient's perspective - Mobility (CHARMI), duration to first independent mobility (days to CHARMI = 6) - ADL (Barthel index) - Hand strength - Muscle strength using knee extension - Length of stay in hospital and in early rehabilitation - Transfer/discharge environment - Sex - Age - BMI - Main diagnosis group, secondary diagnoses, procedures - Therapy units in early rehabilitation	—

Measure

Time frame

- Safety (MTT-associated complication rate) - Feasibility (user survey) - Usability from the perspective of the physiotherapist - Usability from patient's perspective - Mobility (CHARMI), duration to first independent mobility (days to CHARMI = 6) - ADL (Barthel index) - Hand strength - Muscle strength using knee extension - Length of stay in hospital and in early rehabilitation - Transfer/discharge environment - Sex - Age - BMI - Main diagnosis group, secondary diagnoses, procedures - Therapy units in early rehabilitation

—

Countries

Germany

Contacts

Public ContactAnett Reißhauer

Charité Universitätsmedizin Berlin, Arbeitsbereich Physikalische Medizin

anett.reisshauer@charite.de+49 30 450 517082

Outcome results

None listed

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