Evaluating Syde® Digital Health Technology in Healthy Adults
Prospective Longitudinal Multicentric Study to Evaluate Syde® Digital Endpoints in Healthy Adults
This study is testing a digital health tool to see how it can help track health data in healthy adults aged 18 to 65 over two years.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 150 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Sysnav Industry-sponsored |
| Locations | 4 sites (Bron and 3 other locations) |
| Trial ID | NCT06679608 on ClinicalTrials.gov |
What this trial studies
This study aims to create a longitudinal dataset using Syde® digital health technology to establish reference values for healthy adults. Participants will be assessed every six months over a two-year period to gather data on various digital health variables. The study focuses on individuals aged 18 to 65 with a BMI between 17 and 35, who have internet access and can comply with study procedures. The goal is to validate and develop digital endpoints that can be used in future health assessments.
Who should consider this trial
Good fit: Ideal candidates are healthy adults aged 18 to 65 with a BMI between 17 and 35 who can comply with study requirements.
Not a fit: Patients who are elite athletes, pregnant women, or those with certain medical conditions affecting mobility will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a valuable reference for digital health assessments in healthy adults.
How similar studies have performed: While similar studies using digital health technology have shown promise, this specific approach is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
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
Where this trial is running
Bron and 3 other locations
- Hospices Civils de Lyon - Hôpital Femme Mère Enfant (HFME) — Bron, France (Not_yet_recruiting)
- Hôpital NOVO (Nord-Ouest Val d'Oise) — Pontoise, France (Not_yet_recruiting)
- CHU ROUEN - Hôpital Charles Nicolle — Rouen, France (Not_yet_recruiting)
- Sysnav — Vernon, France (Recruiting)
Study contacts
- Study coordinator: Ferial Toumi
- Email: ferial.toumi@sysnav.fr
- Phone: +33 2 78 00 10 98
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.