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Validation of the Mobility Monitor for detecting mobility related activities

Validation of the Mobility Monitor for detecting mobility related activities - Mobility Monitor: technical validity and practical feasibility

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON36479
Enrollment
20
Registered
2011-09-07
Start date
2011-06-17
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Geen, in basis gezonde ouderen als proefpersonen. Niet van toepassing

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - 70 up to and including 80 years of age - Community-dwelling - Be able to walk at least 10m, unsupported or using a walking device such as a cane or rollator

Exclusion criteria

Exclusion criteria: - Total hip replacement surgery in the previous 6 months - Visual problems to a degree that makes it impossible for the subject to accurately read the questionnaires or walk around safely - Having had a stroke within the last 6 months - Parkinson*s disease stage 4 or 5 - Other neurologic diseases that can impair daily functioning (for instance dementia).

Design outcomes

Primary

MeasureTime frame
The main endpoint is to determine whether the Mobility Monitor detects the mobility categories adequately, with a sensitivity and specificity of at least 90%.

Secondary

MeasureTime frame
A secondary goal is to assess user acceptance and practical feasibility of the device, by means of a questionnaire. A third goal is to compare two subjective, self-report means of past physical activity (the SQUASH and PASE questionnaires) and objective measurement of physical activity with the Mobility Monitor.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)