Ireland
--:--IST
Active, not recruiting Observational

Prospective Longitudinal Multicentric Study to Evaluate Syde® Digital Endpoints in Healthy Adults

NCT06679608 · tracked via the Priya Life Science France tracker
Sponsor
Phase
Observational
Started
2025-01-20
Last updated
2026-01-29

Condition(s) studied

Healthy Adults

Study summary

The study aims to constitute a longitudinal Syde® digital health technology (DHT) dataset to serve as a healthy adult reference for Syde® digital variables development and validation. Subjects will be assessed every 6 months for 2 years.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Male or female aged between 18 and 65 years old * Signed informed consent * Subjects with a reported BMI ≥ 17 and ≤ 35 * Subject with unlimited internet connection at home and authorizing automatic data upload * Subject willing and able to comply with all study procedures including: * baseline data and questionnaires data entry on EDC (electronic data capture) throughout the study * Syde® related procedures * Subject confirming to be affiliated to, or beneficiary from, a social security category Exclusion Criteria: * Elite athletes (at a national level) * Pregnant women * Presence of an orthopedic, neuromuscular, or neurological pathology affecting walking gait quality or requiring a walking aid * Subjects reporting to have an incapacity or invalidity or to be affected by a chronic disease which can affect their activity and/or their lower limb function * Subjects reporting to have undergone recent surgical procedures, trauma (within 6 months), or affected by a disease or condition affecting lower limb function within 3 weeks before their inclusion

Primary outcome measure(s)

  • Longitudinal change of SV95C (stride velocity 95th centile) — 2 years
    Change of SV95C between baseline and Month 6, Month 12, Month 18 and Month 24.

Trial sites (4)

FacilityCityRegionStatus
Hospices Civils de Lyon - Hôpital Femme Mère Enfant (HFME) Bron France
Hôpital NOVO (Nord-Ouest Val d'Oise) Pontoise France
CHU ROUEN - Hôpital Charles Nicolle Rouen France
SYSNAV Vernon France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06679608 on ClinicalTrials.gov ↗ ← All trials in France