Informations générales (source: ClinicalTrials.gov)

NCT06679608 Active, sans recrutement
Prospective Longitudinal Multicentric Study to Evaluate Syde® Digital Endpoints in Healthy Adults
Observational
janvier 2025
décembre 2027
02 février 2026
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.

Etablissements

Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données
HOPITAL NOVO WILD Pauline En recrutement IDF 18/09/2025 17:50:07  Contacter
Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
HOPITAL NOVO Contact (sur clinicalTrials)
Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
CHU ROUEN - Hôpital Charles Nicolle - 76000 - Rouen 2982652 - France Contact (sur clinicalTrials)
Hospices Civils de Lyon - Hôpital Femme Mère Enfant (HFME) - 69500 - Bron 3029931 - France Contact (sur clinicalTrials)
Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
SYSNAV - 27200 - Vernon 2969766 - France Contact (sur clinicalTrials)

Critères

Tous


- 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