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Clinical Trials/NCT05179330
NCT05179330CompletedNot Applicable

Visual Feedback in Lower Limb Rehabilitation: the Alpha and the OMEGO®

Fondazione Policlinico Universitario Agostino Gemelli IRCCS1 site in 1 country24 target enrollmentStarted: October 13, 2020Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
24
Locations
1
Primary Endpoint
Change of Symmetry after the performance of the motor task

Study Overview

Brief Summary

Severe Acquired Brain Injury (sABI) is defined as "an encephalic impairment that occurs after birth and is not related to a congenital or degenerative disease.

This impairment may be temporary, or permanent, and cause partial or functional disability or psychosocial distress." In Italy there are at least 10-15 new cases of sABI per year per 100,000 inhabitants; the estimated prevalence is about 150,000 cases per year. Often, people with sABI present focal neurological deficits, including alterations in strength, sensitivity, coordination and gait.

Most of the rehabilitation protocols for people with sABI are derived from post-stroke studies, caused by lack of evidence on specific rehabilitation of people with sABI. Rehabilitation of people with sABI should begin as soon as possible, to prevent the onset of retractions and decubitus, and to regain joint mobility, strength, and coordination.

OMEGO® (Tyromotion) is a newly developed device used in lower extremity rehabilitation, that provides visual and auditory feedback.

Specifically, OMEGO® contains several games developed to enhance and promote learning behaviors, that simulate activities of daily living. The use of devices such as cycle ergometers is recommended in the rehabilitation of people with sABI; however, there are no studies demonstrating the effect of cycle ergometer training in association with visual feedback.

The purpose of this study is to evaluate, both in people without apparent pathology (hereafter identified as "healthy") and in people with sABI, whether visual feedback during OMEGO® exercise modifies brain connectivity, emotional drive, and lower limb performance during a lower limb-specific motor rehabilitation task.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Diagnosis os severe Acquired Brain Injury (sABI)
  • •Trunk Control Test score greater or equal to 48
  • •Motricity Index Lower Limb score greater or equal to 18
  • •Clinical stability
  • •Patient/Caregiver ability to understand ans sing the informed consent

Exclusion Criteria

  • •Disorder of consciousness (mininally concious state or vegetative state)
  • •severe visual impairment (central or peripheral, prior or acquired after the scute event)
  • •presence of severe cognitive impairment
  • •presence of global aphasia or presence of severe apraxia

Arms & Interventions

Group A (no visual feedback-visual feedback)

Experimental

Participants in group A (6 patients with sABI and 6 healthy controls), will perform a single rehabilitation session with OMEGO®. In total, they will perform 18 minutes divided as follows: 5 minutes of treatment with OMEGO® without visual feedback, 3 minutes of break, and additional 5 minutes of treatment with OMEGO® plus visual feedback

Intervention: OMEGO® (Device)

Group B (visual feedback-no visual feedback)

Experimental

Participants in group B (6 patients with sABI and 6 healthy controls), will perform a single rehabilitation session with OMEGO®. In total, they will perform 18 minutes divided as follows: 5 minutes of treatment with OMEGO® plus visual feedback, 3 minutes of break, and additional 5 minutes of treatment with OMEGO® without visual feedback

Intervention: OMEGO® (Device)

Outcomes

Primary Outcomes

Change of Symmetry after the performance of the motor task

Time Frame: Change from baseline at T4 [after 18 minutes]

The symmetry between lower limbs will be evaluated, comparing the percentage of movement between limbs.

Secondary Outcomes

  • Heart Rate Variability(Baseline [T0]; after 5 minutes [training1, T1], after 8 minutes [rest, T2]; after 13 minutes [training2,T3] and after 18 minutes [rest, T4])
  • Change of Proprioception(Change from baseline at T4 [after 18 minutes])
  • Brain connectivity(Baseline [T0]; after 5 minutes [training1, T1], after 8 minutes [rest, T2]; after 13 minutes [training2,T3] and after 18 minutes [rest, T4])
  • Electrodermal activity(Baseline [T0]; after 5 minutes [training1, T1], after 8 minutes [rest, T2]; after 13 minutes [training2,T3] and after 18 minutes [rest, T4])

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

PADUA LUCA

Associated Professor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Study Sites (1)

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