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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UNKNOWN
NA
50 participants
INTERVENTIONAL
2022-10-11
2024-12-31
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
PREVENTION
DOUBLE
Study Groups
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Control Group
Participants randomly assigned to control group will not wear an exoskeleton during working hours.
No interventions assigned to this group
Exoskeleton Group
Participants randomly assigned to exoskeleton group will be given instructions and explanations on how to use/adjust/loosen the exoskeleton, and after a period of familiarisation, they will be wearing an exoskeleton during their working hours for a period of one year.
Exoskeleton
Lumbar assistive exoskeleton evaluation
Interventions
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Exoskeleton
Lumbar assistive exoskeleton evaluation
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* presence of condition that prevents from the use of a lumbar exoskeleton
18 Years
ALL
Yes
Sponsors
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Diputación Foral de Bizkaia
UNKNOWN
University of the Basque Country (UPV/EHU)
OTHER
Responsible Party
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Maialen Aiestaran, MsC
Principal Investigator
Principal Investigators
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Ana Rodriguez Larrad, PhD
Role: STUDY_DIRECTOR
Professor
Locations
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IFAS/GUFE Centro Asistencial Leioa
Leioa, Bizkaia, Spain
IFAS/GUFE Centro Asistencial Elorrio
Elorrio, Vizcaya, Spain
Countries
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Central Contacts
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Facility Contacts
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Role: primary
Other Identifiers
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ExoCare
Identifier Type: -
Identifier Source: org_study_id
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