Validation of the Mobility Monitor for detecting mobility related activities
Recruiting
- Conditions
- Geen, in basis gezonde ouderen als proefpersonen.Niet van toepassing
- Registration Number
- NL-OMON36479
- Lead Sponsor
- niversitair Medisch Centrum Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 20
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
- 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).
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>The main endpoint is to determine whether the Mobility Monitor detects the<br /><br>mobility categories adequately, with a sensitivity and specificity of at least<br /><br>90%. </p><br>
- Secondary Outcome Measures
Name Time Method <p>A secondary goal is to assess user acceptance and practical feasibility of the<br /><br>device, by means of a questionnaire. A third goal is to compare two subjective,<br /><br>self-report means of past physical activity (the SQUASH and PASE<br /><br>questionnaires) and objective measurement of physical activity with the<br /><br>Mobility Monitor.</p><br>