Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07136506

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Centre de référence des maladies neuromusculaire, Centre Hospitalier Régional de la Citadelle

Liège, Belgium, 4000

Actively Recruiting

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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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