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Mobility measures in neurorehabilitation trial – MOMENT

Mobility measures in neurorehabilitation trial – MOMENT - MOMENT

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00018917
Enrollment
280
Registered
2019-10-16
Start date
2019-10-21
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

Inpatients with CNS disorders G00-G99

Interventions

Group 1: Mobility of all patients (participants) will be assessed three times within routine physiotherapy procedures (standard of care within the hospital): - hospital admission - follow-up after 4 w

Sponsors

Rehaklinik Zihlschlacht
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Inpatient stay in the rehabilitation clinic due to CNS disease 2. Age at least 18 years

Exclusion criteria

Exclusion criteria: 1. No physiotherapeutic routine data available. This is e.g. the case when the patient's medical condition does not allow physical examination by a physiotherapist or such an examination would endanger the patient. Also in patients with severe aphasia / apathy, apraxia and / or other psycho-cognitive symptoms, motor examinations may not be possible due to the lack of / limited understanding of the task. 2. Patients who refuse to use their health-related personal data for research purposes.

Design outcomes

Primary

MeasureTime frame
In order to determine the psychometric properties of these measuring instruments of mobility, the following investigations are carried out. All analyzes are informed by the methodological recommendations of the COSMIN group [COnsensus-based Standards for the selection of health Measurement Instruments; Terwee et al. 2007; de Vet et al. 2011; Mokkink et al. 2010]. Primary outcome: Prognostic validity: Calculation of the prognostic validity (criterion approach) of the individual measuring instruments with regard to the following health-related outcomes at the time 4 weeks after admission: fall frequency, modified ranking scale, Barthel index, length of stay, ability to walk, discharge destination).

Secondary

MeasureTime frame
Secondary outcomes: Construct validity: Method of hypothesis testing (correlations of measuring instruments among each other) as well as know-groups-validity analyzes. Sensitivity to change: Repetition of tests at follow-up 4 weeks after admission to the clinic as well as immediately before leaving the clinic plus recording of a "Global Rating of Change" (assessment of the subjectively perceived change in patient mobility). Calculating responsiveness using the construct and anchor-based approach. Interpretability: Floor and ceiling effects are described descriptively. Calculation of the "minimal important change" values for all measurement instruments (MIC) using anchor-based methods.

Countries

Switzerland

Contacts

Public ContactDetlef Marks

Rehaklinik Zihlschlacht

d.marks@rehaklinik-zihlschlacht.ch+41 (0) 71 424 37 51

Outcome results

None listed

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