Actively Recruiting
Gait Analysis Parameter and Upper Limb Evaluation in Control Participants
Led by Centre Hospitalier Universitaire de Liege · Updated on 2025-12-02
200
Participants Needed
1
Research Sites
166 weeks
Total Duration
On this page
Sponsors
C
Centre Hospitalier Universitaire de Liege
Lead Sponsor
C
Centre Hospitalier Régional de la Citadelle
Collaborating Sponsor
AI-Summary
What this Trial Is About
The ActiControl study is a monocentric, academic, and fully remote observational study designed to build a normative, longitudinal dataset using the Syde® wearable device. The study will enroll 200 healthy volunteers across all age groups, genders, and backgrounds. Participants will be remotely recruited and followed over two years, wearing the Syde® device for 3-week periods every 6 months. All study visits, including consent, data collection, and follow-up, are conducted remotely via phone or video conferencing. The primary objectives are to collect reference data on gait and movement patterns and to assess adherence and acceptability of the device. Secondary objectives include evaluating the reliability of digital endpoints and the influence of demographic and lifestyle factors on these measures.
CONDITIONS
Official Title
Gait Analysis Parameter and Upper Limb Evaluation in Control Participants
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male and female of different age groups
- Signed informed consent form by participant or legal guardian if under 18 years old
- Able to walk at least 10 meters without help
- Body mass index (BMI) between 17 and 30
- Willing and able to follow all study procedures
You will not qualify if you...
- Surgery or trauma affecting upper or lower limbs within the past 6 months
- Elite athletes competing at the national level
- Pregnant women
- Any chronic or acute muscle, neurological, infectious, or inflammatory condition within 3 weeks before inclusion
- Orthopedic, neuromuscular, or neurological condition affecting walking quality
- No access to unlimited internet or unable to upload Syde data on-site
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Centre de référence des maladies neuromusculaire, Centre Hospitalier Régional de la Citadelle
Liège, Belgium, 4000
Actively Recruiting
Research Team
N
Nicolas Bovy
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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