Status:
UNKNOWN
Validity of the Kinect™ Sensor for Measuring Range of Motion in Patients Post-stroke and Healthy Test Subject
Lead Sponsor:
Vrije Universiteit Brussel
Conditions:
Stroke
Healthy
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The aim of this research is to investigate the validity of the Kinect™ sensor in post-stroke patients and in healthy test subjects during analytic and functional movements. Measurements will be compar...
Detailed Description
STUDY DESIGN This study is a cross-sectional study in which healthy people and people post stroke will perform 1 session where we will investigate the validity of the Kinect sensor. MATERIALS 1. Th...
Eligibility Criteria
Inclusion
- People post-stroke or healthy test subjects
- Language: Dutch, English or French
- Age ≥ 18
- Able to sit and stand unsupported for 30 s or more
- Able to stand up from a chair without aid of another person
- Able to signal pain, fear of discomfort
- Able to give informed consent (based on the advice of a medical doctor)
- Able to understand and perform the instructions and to answer questions
Exclusion
- Concurrent orthopedic and/or musculoskeletal pathologies or disorders that may limit the range of motion (including limb amputations)
- Concurrent neurological disorders (e.g. Parkinson's Disease, Multiple Sclerosis or Amyotrophic Lateral Sclerosis)
- Persons with comorbidity that could hinder the study (e.g. unstable cardiovascular system disorders, lung disorders, severe osteoporosis)
- People with difficulties of speech and/or memory providing that instruction cannot be followed or understood adequate
Key Trial Info
Start Date :
April 14 2022
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2024
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT05295654
Start Date
April 14 2022
End Date
December 31 2024
Last Update
October 19 2022
Active Locations (1)
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1
Brubotics Rehabilitation Research Center
Brussels, Belgium, 1090