MedTrace Logo

Action Observation Training for Upper Limb Rehabilitation in Stroke Patients

NCT04622189 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2022-05-25

No results posted yet for this study

Summary

The purpose of this study is to assess the changes in physiological parameters and clinical scales resulting from treatment with AOT (action observation training) in subjects with subacute stroke. Furthermore, this study assess the perception of applicability and satisfaction degree for this kind of treatments.

Conditions

  • Stroke Rehabilitation

Interventions

DEVICE

Action observation training

Integration of four main tools: * PATIENT INTERFACE, which has been implemented to present stimuli with a user friendly interface, with personalized menu and with the possibility to manage the training program; user personal page containing user information and history of activities with daily performance are stored too. * MOCAP during action imitation will be recorded using MindMotion infrared camera to capture the trunk movement while an electromagnetic system (Trackstar from NDI) will be used to record fingers fine movements. * EEG data will be collected during video observation using an Enobio wireless system integrated with the platform.

Sponsors & Collaborators

  • Istituto Italiano di Tecnologia

    collaborator OTHER

  • University Hospital of Ferrara

    lead OTHER

Principal Investigators

  • Luciano Fadiga, MD, PhD · Section of Human Physiology, University of Ferrara (Ferrara, Italy)

  • Sofia Straudi, MD, PhD · Department of Neuroscience and Rehabilitation, University Hospital of Ferrara (Ferrara, Italy)

  • Thierry Pozzo, PhD · IIT; Istituto Italiano di Tecnologia

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-06-11
Primary Completion
2021-12-09
Completion
2021-12-09

Countries

  • Italy

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04622189 on ClinicalTrials.gov