Gait Analysis Parameter and Upper Limb Evaluation in Control Participants

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.

NCT Number	NCT07136506
Lead Sponsor	Centre Hospitalier Universitaire de Liege Collaborators: Centre Hospitalier Régional de la Citadelle, SYSNAV
Conditions	Healthy Participants
Enrollment	200 participants
Start Date	2025-09-24
Primary Completion	2028-09 (estimated)
Study Completion	2028-12 (estimated)
Updated on ClinicalTrials.gov	2026-05-19