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The main objective of this monocentric, non-randomized, prospective study was to evaluate the predictive capacity of a balance score based on spatio-temporal parameters of postural balance.
Patient recruitment will take place at one center. The inclusion period is 6 months and the participation period for each subject will be 12 months with 3 visits: initial visit, telephone visit at 6 months, M12 consultation visit, and the end-of-study visit. Consent will be obtained prior to participation, and the following data will be collected during the visits: Demographic data (age, gender), weight, height, geriatric assessment. Current treatment (molecules, date of introduction, dosage). Biological data: Albumin, Pre-Albumin, Creatinine, Hemoglobin, Vitamin D. Static balance parameters via AbilyCare (static balance test, inspired by the Romberg test, on a balance platform, 30 seconds eyes open then 30 seconds eyes closed). The total duration of the research is 18 months.
Age
65 - 95 years
Sex
ALL
Healthy Volunteers
Yes
Ambulatory Care Department, Charles Foix Hospital
Ivry-sur-Seine, IIe-de-France, France
Start Date
July 28, 2024
Primary Completion Date
July 23, 2026
Completion Date
January 23, 2027
Last Updated
September 22, 2025
169
ESTIMATED participants
Fall risk assessment
DEVICE
Lead Sponsor
Gérond'if
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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