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Study identifier: NCT06692296 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Efficacy of Stabilometric Platform to Improve Standing Balance in Patients With Friedreich's Ataxia

Condition: Friedreich Ataxia  ·  Sponsor: IRCCS Eugenio Medea

PhaseNA
Planned participants24
Who can joinAll sexes, 14 Years to no upper limit
Healthy volunteersNo

About this study

The primary objective is to evaluate the potential effectiveness of an individualized intensive rehabilitation intervention using the "Prokin 252" stabilometric platform in the treatment of adolescent and adult patients with Friedreich's Ataxia. The secondary objective is to assess the retention of the rehabilitation treatment effects over time. Enrolled patients will be randomized and assigned to one of two treatment groups for four weeks. Three assessments will be conducted for each patient: one before treatment (T0), one at the end of treatment (T1), and a follow-up assessment 90 days after T1 via telemedicine (T2). This study is: * Exploratory: The study aims to explore the usefulness of the stabilometric platform in a rehabilitative setting in combination with conventional therapy; * Not "first-in-human"; * Longitudinal: The study will investigate changes over time in motor and functional ability scales, as well as stabilometric platform parameters, within the same cohort; * Randomized, controlled, open-label; * Monocentric: The study will be conducted only at the "La Nostra Famiglia" Association in Conegliano and Pieve di Soligo - IRCCS Eugenio Medea in Conegliano - UOC Neuromotor Rehabilitation in Pieve di Soligo, Via Monte Grappa, 96, 31053 Pieve di Soligo TV; * Prospective; * Post-market.

This description comes directly from the study's public registry record.

Talk to the study team

Gabriella Paparella, Medical Degree  ·  00390438906330  ·  gabriella.paparella@lanostrafamiglia.it

Always discuss trial participation with your own doctor first.

Locations (1)

Scientific Institute, IRCCS E. Medea, Department of Pieve di Soligo, Treviso, ItalyPieve di Soligo, Veneto, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06692296