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Wearable Robotic Upper Body Exoskeleton for Workers

Ergonomic Evaluation of Workspaces and Occupational Tasks Targeted for Exoskeleton Support and Definition of Case Studies

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03491501
Acronym
Exo4Work
Enrollment
100
Registered
2018-04-09
Start date
2018-07-16
Completion date
2018-12-01
Last updated
2018-05-14

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

Conditions

Mental Fatigue, Physical Stress, Work-Related Condition

Keywords

Industrial work, physical effort, mental effort, questionnaires, ergonomic evaluation

Brief summary

The main aim of the project is to evaluate a novel upper body exoskeleton during simulated industrial work. In a first stage of the project, an extensive study involving the end-user companies will be carried out to clearly identify the operator target tasks and typical target task loads for which the exoskeleton will be designed. Based on standard ergonomic evaluation scales (RULA and NIOSH, the Need for Recovery Scale and the Ovako Working Posture Analysing System), high risk tasks will be identified in the field, based on the evaluated information about the workspace configuration, the performed operations and their physical constraints. These will include, but will not be limited to, non-ergonomic postures, for example performing operations above the head or reaching in front, to the side, or behind the body; flexing the arms for extended periods of time; and bending or twisting the torso to lift an object from low or distant locations. Important items to assess in this task are the frequency and duration of tasks and activities, lifting characteristics, perceived physical effort and work-induced fatigue.

Interventions

OTHERErgonomic evaluation using questionnaires

Employees will be provided with questionnaires such as the 'Rapid Entire Body Assessment' and NIOSH to obtain information regarding ergonomic working situations

Sponsors

Vrije Universiteit Brussel
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

Industrial employees \-

Exclusion criteria

* non-able bodied individuals

Design outcomes

Primary

MeasureTime frameDescription
QuestionnaireThe time point of data collection: An average of 1yrErgonomic evaluation Industrial work situations

Countries

Belgium

Contacts

Primary ContactSander De Bock, Master
Sander.De.Bock@vub.be0032 2 629 22 22

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026