ClinicalTrials.Veeva

Menu

AI-based Model for Rehabilitation Engagement and Motor Performance Evaluation in Pediatric Patients (AI-REMAP)

I

IRCCS Eugenio Medea

Status

Active, not recruiting

Conditions

Neuromotor Impairments

Treatments

Other: Inapplicable

Study type

Observational

Funder types

Other

Identifiers

NCT06993389
RC 2024-2026 to E. Biffi (Other Grant/Funding Number)
L2-246

Details and patient eligibility

About

What is the purpose of this study? This study wants to learn how the physiological signals and movement data can help researchers understand and predict how children with neuromotor impairments engage with rehabilitation.

Who can take part? 40 participants between 5 and 17 years old will take part. Half of them will be children with neurotypical development (control). The other half will be children with neuromotor impairments.

What will happen in the study? Children within the control group will take part in 1 rehabilitation session, while those with neuromotor impairments will take part in 2 to 3 rehabilitation sessions as part of the treatment plan already provided by their referring physicians.

During each session, researchers will collect: (i) physiological signals like heart activity (ECG), heart rate variability (HRV), and electrodermal activity (EDA); (ii) movement data; (iii) exergames scores and motor performance data; (iv) questionnaires filled out by therapists to understand how engaged the participant is.

Children will use one of two technology-assisted rehabilitation systems during their sessions: either the Lokomat (robotic exoskeleton that supports children with impairments in walking) or the GRAIL system (a treadmill system with motion tracking and extended reality).

Why is this study important? Researchers will use the data to understand and predict how each child responds to therapy and engage with it. These analyses will help therapists adjust rehabilitation settings in real-time, offering more personalized and effective care for children with neuromotor impairments.

Enrollment

40 estimated patients

Sex

All

Ages

5 to 17 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Subjects aged between 5 and 17 with typical development.
  • Subjects aged between 5 and 17 years with neuromotor impairments who are undergoing rehabilitation therapy using the Lokomat and GRAIL devices, according to the existing clinical plan.

Exclusion criteria

  • Uncooperative subjects.

Trial design

40 participants in 2 patient groups

Neuromotor impaired
Treatment:
Other: Inapplicable
Control
Treatment:
Other: Inapplicable

Trial contacts and locations

1

Loading...

Central trial contact

Fabio A Storm, PhD; Simone Costantini, MSc

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems