Ankle Fractures Clinical Trial
Official title:
Robot-assisted Ankle Rehabilitation Using the High-performance Robotic Device IIT-ARBOT: A Pilot Randomised Controlled Study
The purpose of this trial is to determine the effectiveness, safety and tolerability of robot-assisted rehabilitation using ARBOT in patients with ankle dysfunction resulting from work related ankle fractures, compared with conventional rehabilitation programs.
INTRODUCTION:
Robotic devices for lower-limb rehabilitation have been mainly tested in neurologically
injured patients. Up to now, clinical studies using robotic training in orthopedic
conditions are few. A pilot study was carried out at INAIL Physical Rehabilitation Center of
Volterra using ARBOT, a prototypal robotic system for ankle rehabilitation. This device has
been developed by IIT - Italian Institute of Technology and it consists of a
two-degree-of-freedom electromechanical platform which is able to perform most of the
exercises foreseen by the standard rehabilitation programs. By virtue of its innovative
motion system and control architecture, ARBOT integrates multiple rehabilitation equipment
functions, performing also special exercise programs such as elastic and fluid-dynamic
resistance.
ARBOT allows training according to programmed sequences, in order to promote range of
movement, muscular function and proprioceptive recovery. Exercises can be performed with or
without bearing weight. Moreover, ARBOT is a powerful evaluation instrument for
physiotherapists in order to verify and record the results of rehabilitative intervention.
The primary aim of this trial was to determine the effectiveness, safety and tolerability of
robot-assisted rehabilitation using ARBOT in patients with ankle dysfunction resulting from
work related ankle fractures, compared with conventional rehabilitation programs. Secondary
objectives was to investigate correlations among physical and disability parameters, to
collect data in order to define further study protocols and improve ARBOT's performance and
ergonomics, and ultimately to evaluate patient satisfaction with respect to robot assisted
rehabilitation programs.
METHODS:
Thirty-two patients with work related injuries resulting in ankle and/or hindfoot fractures
and subsequent to the immobilization phase was enrolled in an open randomized controlled
trial over a 30 month period. Each participant was randomly allocated to experimental or
control group and received a 4-week rehabilitation program (20 sessions, for 5 days/week
from admission to discharge in the Rehabilitation Centre) and weekly robotic and clinical
assessments.
Subjects in the experimental group were treated using ARBOT with passive, active and active
assisted range-of-motion exercises, resistive exercises in isometric, isotonic, isokinetic,
elastic and fluid-dynamic conditions, and proprioceptive training. Control subjects were
assisted by a physiotherapist during range of motion recovery exercises and performed
resistive and proprioceptive training using Biodex System 3 dynamometer and ProKin PK254
mobile electronic platform.
The assessment sessions included measurements of dorsiflexion ROM, isometric and isokinetic
plantar-flexion torque and proprioceptive performance with ARBOT and 2 minutes walking and
timed stair climbing test, LEFS-Lower Extremity Functional Scale and AOFAS-Ankle-Hindfoot
Scale.
Site monitoring of the study has been conducted according to the standard ISO 14155.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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