Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
21 participants
INTERVENTIONAL
2015-11-30
2016-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SINGLE
Study Groups
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A additional BioRescue training
Using a playful rehabilitation, BioRescue
Biorescue training
Regular training
No interventions assigned to this group
Interventions
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Biorescue training
Eligibility Criteria
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Inclusion Criteria
* Participants with increased fall-risk (i.e. Timed Up-and-Go Test (TUG) \> 20 sec)
* Participants with Mild Cognitive Impairment (MCI) measured by the Montreal Cognitive Assessment (MoCa \< 25). MCI: A state of altered cognition, characterized by a decline in one or more cognitive domains, typically including memory while the independence for daily activities remains intact.
* Participants have a positive result on the 'Stops Walking While Talking' test
Exclusion Criteria
* In rehabilitation for a recent injury or recent prothesis of the upper or lower extremities.
* Serious limitations of the lower and or upper limb.
* Not able to walk more than 10 meters independently (walking-aid allowed).
65 Years
ALL
No
Sponsors
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Hasselt University
OTHER
Responsible Party
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Peter Feys
prof. dr.
Principal Investigators
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Peter Feys, prof. dr.
Role: PRINCIPAL_INVESTIGATOR
Hasselt University
Locations
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Hasselt University
Diepenbeek, , Belgium
Woon- en zorgcentrum Sint Elisabeth
Hasselt, , Belgium
Countries
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Other Identifiers
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2015-PFE-JSP-01
Identifier Type: -
Identifier Source: org_study_id
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