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Trial · NCT07389018

Registered outcomes12

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNumber of patients reaching the optimal threshold of recordings during the recording periods defined in the protocol.16 months
Number of patients reaching the optimal threshold of recordings during the recording periods defined in the protocol (supposed optimal threshold for analysis) at baseline, Month 4, Month 8, Month 12 and Month 16.
PrimaryFrench Usability score (F-SUS) at Month 4 and at the end of the study16 months
Usability score at Month 4 and Month 16. The System Usability Scale is a 10-item questionnaire . It is a simple tool to measure the usability of an interactive system and it is widely used. For each item, the user is asked to express their level of agreement or disagreement from 1 (strongly disagree) and 5 (strongly agree).
SecondaryChange from baseline in the total wearing time at months 4, 8, 12, and 16.16 monthsChange from baseline in the total wearing time at months 4, 8, 12, and 16.
SecondaryReproducibility of Syde® digital endpoints for each recording period timepoint16 months
Reproducibility of Syde® digital endpoints assessed by the ICC (Intra-Class Correlation) and Bland and Altman analysis for each recording period timepoint (baseline, 4 months, 8 months, 12 months, and 16 months)
SecondaryCorrelation between Syde® digital endpoints and 2-minute walk test (2MWT)16 monthsCorrelation at baseline and at different timepoints between Syde® digital endpoints and 2MWT
SecondaryCorrelation between Syde® digital endpoints and 10-meter walk test (10MWT)16 monthsCorrelation at baseline and at different timepoints between Syde® digital endpoints and 10MWT
SecondaryCorrelation between Syde® digital endpoints and Timed Up and Go (TUG)16 monthsCorrelation at baseline and at different timepoints between Syde® digital endpoints and TUG
SecondaryCorrelation between Syde® digital endpoints and falls reported by the participants16 monthsCorrelation at baseline and at different timepoints between Syde® digital endpoints and falls reported by the participants
SecondaryCorrelation between Syde® digital endpoints and Progressive Supranuclear Palsy Rating Scale (PSP-RS)16 monthsCorrelation at baseline and at different timepoints between Syde® digital endpoints and PSP-RS
SecondaryCorrelation between Syde® digital endpoints and Progressive Supranuclear Palsy Clinical Deficits Scale (PSP-CDS)16 monthsCorrelation at baseline and at different timepoints between Syde® digital endpoints and PSP-CDS
SecondaryCorrelation between Syde® digital endpoints and Montreal Cognitive Assessment (MoCA)16 monthsCorrelation at baseline and at different timepoints between Syde® digital endpoints and MoCA
SecondaryLongitudinal change in Syde® digital endpoints. The Syde® digital endpoints will include the SV95C (Stride Velocity 95th centile)16 monthsChange from baseline in Syde® digital endpoints at 4, 8, 12 and 16 months. The Syde® digital endpoints will include the SV95C (Stride Velocity 95th centile)

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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