Informations générales (source: ClinicalTrials.gov)
Prospective Longitudinal Multicentric Study to Evaluate Syde® Digital Endpoints in Healthy Adults (Syde-CAR)
Observational
SYSNAV (Voir sur ClinicalTrials)
janvier 2025
janvier 2028
05 avril 2025
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 | 14/02/2025 09:03:20 | Contacter | ||
| Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
| CHU ROUEN - Hôpital Charles Nicolle - 76000 - Rouen - France | Marie-Pierre TAVOLACCI, MD, PhD | Contact (sur clinicalTrials) | |||
| Hospices Civils de Lyon - Hôpital Femme Mère Enfant (HFME) - 69500 - Bron - France | Shotaro TACHIBANA, PT | Contact (sur clinicalTrials) | |||
| SYSNAV - 27200 - Vernon - France | Shotaro TACHIBANA, PT | Contact (sur clinicalTrials) | |||
Critères
Tous
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
- 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
- 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