Quantitative Assessment of Training Effects Using EKSOGT Exoskeleton in Quantitative Assessment of Training Effects Using EKSOGT Exoskeleton in Parkinson Disease Patients (Ekso_PD)
Primary Purpose
Parkinson Disease
Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Experimental: EksoGT
Functional kinematic training
Sponsored by
About this trial
This is an interventional treatment trial for Parkinson Disease focused on measuring Parkinson Disease, rehabilitation exhoskeleton, gait analysis, fMRI, Electroencephalogram
Eligibility Criteria
Inclusion Criteria:
- Patient with rigid-acinetic bilateral PD form
- Hoehn-Yahr between 3-4
- At least 4 years of disease history
- Stable drug therapy response without any change performed in the 3 months before the study
- Presence of freezing (FOG) and of postural instability not responding to parkinsonian therapy
- Mini Mental State Evaluation > 24/30
Exclusion Criteria:
- Systemic illness
- Presence of cardiac pacemaker
- Postural abnormalities, orthopedic comorbidities that do not match the active physiotherapy treatment
- Presence of deep brain stimulation
- Presence of severe disautonomia with marked hypotension
- Obsessive-Compulsive disorder (OCD)
- Major depression
- Dementia and psychosis
- History or active neoplasia
- Pregnancy
- Other criteria that do not respect the device counterindications
Sites / Locations
- University of PadovaRecruiting
- Fresco Parkinson Center, Villa MargheritaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
EksoGT
Functional kinematic training
Arm Description
Device: EksoGT. EksoGT is an overground wearable gait trainer. The therapy will be carried out 3 days a week for 4 weeks.
Device: No device. The functional kinematic training will be delivered as comparator treatment and will be carried out 3 days a week for 4 weeks.
Outcomes
Primary Outcome Measures
Change in joint kinematics after 30 days
Joint kinematics (degrees): trunk, pelvis, hip, knee, ankle (flexion-extension, ab-adduction, internal - external rotation)
Change in joint kinematics after 60 days
Joint kinematics (degrees): trunk, pelvis, hip, knee, ankle (flexion-extension, ab-adduction, internal - external rotation)
Change in Spatiotemporal parameters after 30 days - Gait velocity
Gait velocity (meters/seconds)
Change in Spatiotemporal parameters after 60 days - Gait velocity
Gait velocity (meters/seconds)
Change in Spatial parameters after 30 days
Step width (meters), step length (meters)
Change in Spatial parameters after 60 days
Step width (meters), step length (meters)
Change in Temporal parameters after 30 days
Step duration (seconds), gait period (seconds),stance period (seconds), swing period (seconds), double support (seconds)
Change in Temporal parameters after 60 days
Step duration (seconds), gait period (seconds),stance period (seconds), swing period (seconds), double support (seconds)
Change in Spatiotemporal parameters after 30 days - Cadence
Cadence (steps/minute)
Change in Spatiotemporal parameters after 60 days - Cadence
Cadence (steps/minute)
Change in balance after 30 days - center of pressure spatial parameters
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean distance from centre of COP trajectory (mm), root mean square of COP time series (mm), sway path, total COP trajectory length (mm), range of COP displacement (mm).
Change in balance after 60 days - center of pressure spatial parameters
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean distance from centre of COP trajectory (mm), root mean square of COP time series (mm), sway path, total COP trajectory length (mm), range of COP displacement (mm)
Change in balance after 30 days - center of pressure velocity
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean COP velocity (mm/s)
Change in balance after 60 days - center of pressure velocity
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean COP velocity (mm/s)
Change in balance after 30 days - center of pressure frequency
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean frequency (Hz), i.e., number, per second, of loops that have to be run by COP to cover total trajectory equal to sway path ; median frequency (Hz), frequency below which 50% of total power is present; 95% power frequency (Hz), frequency below which 95% of total power is present, centroidal frequency (Hz), frequency at which spectral mass is concentrated.
Change in balance after 60 days - center of pressure frequency
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean frequency (Hz), i.e., number, per second, of loops that have to be run by COP to cover total trajectory equal to sway path ; median frequency (Hz), frequency below which 50% of total power is present; 95% power frequency (Hz), frequency below which 95% of total power is present, centroidal frequency (Hz), frequency at which spectral mass is concentrated.
Change in balance after 30 days - center of pressure ellipse parameters
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: area of 95% confidence circumference (mm^2), area of 95% confidence ellipse (mm^2).
Change in balance after 60 days - center of pressure ellipse parameters
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: area of 95% confidence circumference (mm^2), area of 95% confidence ellipse (mm^2).
Change in balance after 30 days - center of pressure sway area
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: sway area, computed as area included in COP displacement per unit of time (mm^2/seconds).
Change in balance after 60 days - center of pressure sway area
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: sway area, computed as area included in COP displacement per unit of time (mm^2/seconds).
Change in muscle forces after 30 days
Musculotendon forces estimated via musculoskeletal modeling (OpenSim, CEINMS)
Change in muscle forces after 60 days
Musculotendon forces estimated via musculoskeletal modeling (OpenSim, CEINMS)
Secondary Outcome Measures
Change in Movement Disorder Society - Unified Parkinson Disease Rating Scale (MDS-UPDRS) after 30 days
MDS-UPDRS in all its four components (0 no disability - 199 total disability)
Change in Movement Disorder Society - Unified Parkinson Disease Rating Scale (MDS-UPDRS) after 60 days
MDS-UPDRS in all its four components (0 no disability - 199 total disability)
Change in Timed Up and Go test (TUG) after 30 days
Timed Up and Go test (TUG) (>= 12 seconds risk of falling).
Change in Timed Up and Go test (TUG) after 60 days
Timed Up and Go test (TUG) (>= 12 seconds risk of falling).
Change in Berg Balance Scale (BBS) after 30 days
Berg Balance Scale (BBS) (56 functional balance, < 45 greater risk of falling).
Change in Berg Balance Scale (BBS) after 60 days
Berg Balance Scale (BBS) (56 functional balance, < 45 greater risk of falling).
Change in Falls Efficacy Scale (FES) after 30 days
Falls Efficacy Scale (FES) (16 severe concern about falling - 64 no concern about falling).
Change in Falls Efficacy Scale (FES) after 60 days
Falls Efficacy Scale (FES) (16 severe concern about falling - 64 no concern about falling).
Change in 6 minutes walking test (6-WT) after 30 days
6 minutes walking test (6-WT) (min 311 meters - max 673 meters)
Change in 6 minutes walking test (6-WT) after 60 days
6 minutes walking test (6-WT) (min 311 meters - max 673 meters)
Change in Ziegler Protocol for the assessment of Freezing of Gait (FOG) severity after 30 days
Ziegler Protocol for the assessment of FOG severity (0 no festination, no FOG - 1 festination - 2 FOG).
Change in Ziegler Protocol for the assessment of Freezing of Gait (FOG) severity after 60 days
Ziegler Protocol for the assessment of FOG severity (0 no festination, no FOG - 1 festination - 2 FOG).
Change The New Freezing of Gait Questionnaire (N-FOGQ) severity after 30 days
The New Freezing of Gait Questionnaire (N-FOGQ) (0 never happened, 4 unable to walk for more than 30s).
Change The New Freezing of Gait Questionnaire (N-FOGQ) severity after 60 days
The New Freezing of Gait Questionnaire (N-FOGQ) (0 never happened, 4 unable to walk for more than 30s).
Change in neurophysiological assessment after 30 days : electromyography (EMG)
Magnitude (milliVolt)
Change in neurophysiological assessment after 60 days : electromyography (EMG)
Magnitude (milliVolt)
Change in neurophysiological assessment after 30 days : electroencephalogram (EEG)
Spectral parameters (Hz)
Change in neurophysiological assessment after 60 days : electroencephalogram (EEG)
Spectral parameters (Hz)
Change in neurophysiological assessment after 30 days : functional Magnetic Resonance Imaging (fMRI)
Number of active voxel in the region of interest
Change in neurophysiological assessment after 60 days : functional Magnetic Resonance Imaging (fMRI)
Number of active voxel in the region of interest
Full Information
NCT ID
NCT04778852
First Posted
November 30, 2020
Last Updated
May 9, 2023
Sponsor
University of Padova
Collaborators
Fresco Parkinson Center Villa Margherita, Vicenza, Italy, Fresco Institute for Parkinson's & Movement Disorders, NYU Langone
1. Study Identification
Unique Protocol Identification Number
NCT04778852
Brief Title
Quantitative Assessment of Training Effects Using EKSOGT Exoskeleton in Quantitative Assessment of Training Effects Using EKSOGT Exoskeleton in Parkinson Disease Patients
Acronym
Ekso_PD
Official Title
Quantitative Assessment of Training Effects Using a Wearable Exoskeleton in Parkinson Disease Patients
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 12, 2020 (Actual)
Primary Completion Date
June 12, 2022 (Actual)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Padova
Collaborators
Fresco Parkinson Center Villa Margherita, Vicenza, Italy, Fresco Institute for Parkinson's & Movement Disorders, NYU Langone
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
The ability to walk independently is a primary goal when rehabilitating an individual with Parkinson Disease (PD). Indeed, PD patients display a flexed posture that coupled with an excessive joint stiffness lead to a poor walking mechanics that increase their risk of falls. Although studies have already shown the many benefits of robotic-assisted gait training in PD patients, research focusing on optimal rehabilitation methods has been directed towards powered lower-limb exoskeleton. Combining the advantages delivered from the grounded devices with the ability to train in a real-world environment, these systems provide a greater level of subject participation and increase subject's functional abilities while the wearable robotic system guarantees less support. The purpose of the present work is to evaluate the effects of an Over-ground Wearable Exoskeleton Training (OWET) on gait impairments in comparison with a multidisciplinary intensive rehabilitation treatment. As gait is a complex task that involves both central (CNS) and peripheral nervous systems (PNS), targeted rehabilitation must restore not only gait mechanics (ST parameters) but also physiological gait pattern (joint kinematics and dynamics). To this aim the impact of OWET on both CNS and PNS will be evaluated. Thus, a quantitative assessment of an individual's gait and neuromuscular function to robustly evaluate recovery of altered sensorimotor function at both the PNS and CNS is proposed. To this aim, comprehensive GA (spatiotemporal (ST) parameter, joint kinematics, joint stiffness) and electromyography (EMG) will be combined to determine PNS improvements, and fMRI with EEG will be used to assess CNS improvements.
Detailed Description
Full Title: QUANTITATIVE ASSESSMENT OF TRAINING EFFECTS USING A WEARABLE EXOSKELETON IN PARKINSON DISEASE PATIENTS
RESEARCH PLAN
Specific Aims
The ability to walk independently is a primary goal when rehabilitating an individual with Parkinson Disease (PD). Indeed, PD patients display a flexed posture that coupled with an excessive joint stiffness lead to a poor walking mechanics that increase their risk of falls. Although studies have already shown the many benefits of robotic-assisted gait training in PD patients, research focusing on optimal rehabilitation methods has been directed towards powered lower-limb exoskeleton. Combining the advantages delivered from the grounded devices with the ability to train in a real-world environment, these systems provide a greater level of subject participation and increase subject's functional abilities while the wearable robotic system guarantees less support. The purpose of the proposed work is to evaluate the effects of an Over-ground Wearable Exoskeleton Training (OWET) on gait impairments in comparison with a multidisciplinary intensive rehabilitation treatment. As gait is a complex task that involves both central (CNS) and peripheral nervous systems (PNS), targeted rehabilitation must restore not only gait mechanics (ST parameters) but also physiological gait pattern (joint kinematics and dynamics). To this aim the impact of OWET on both CNS and PNS will be evaluated. Human movement analysis quantitatively assesses the neuromuscular and biomechanical features of movement. Recent literature has highlighted the benefit of coupling gait analysis (GA) and neuromusculoskeletal modeling (NMSM) for treatment planning and supplementing this approach with robotic rehabilitation. Another stalwart of PD research has been electroencephalography (EEG), which is widely used to evaluate executive dysfunction while functional magnetic resonance imaging (fMRI) can detect cortical changes in motor activations during motor tasks. Thus, a quantitative assessment of an individual's gait and neuromuscular function to robustly evaluate recovery of altered sensorimotor function at both the PNS and CNS is proposed. To this aim, comprehensive GA (spatiotemporal (ST) parameter, joint kinematics, joint stiffness) and electromyography (EMG) will be combined to determine PNS improvements, and fMRI with EEG will be used to assess CNS improvements. As health care professionals and researchers need objective, reliable, and valid tools to plan subject-specific interventions, quantify therapeutic outcomes, and monitor change over time, the proposed study includes estimation of neutrally-informed muscle forces and joint stiffness, which is expected to provide sensitive determinants of PD movement control that could be crucial to inform treatment planning/assessment. Preliminary data are available and showed feasibility of the proposed measurement set up.
Background OWET: Although studies have already shown the many benefits of robotic-assisted gait training in PD patients (i.e. body weight supported treadmill training) as improving gait efficiency modifying spatiotemporal (ST) parameters, these strategies create an environment where the patient has less control over the gait initiation and lacks in variability of visuospatial flow. Therefore, research focusing on optimal rehabilitation methods has been directed towards powered lower-limb exoskeleton, as in post-stroke rehabilitation, where the effect of such a treatment dramatically enhanced potential for patient-specific rehabilitation, showing improvement in ST parameters. Combining the advantages delivered from the grounded robotic devices with the ability to train the patient in a real-world environment, these systems provide a greater level of subject participation for maintaining trunk and balance control, as well as navigating their path over different surfaces and increase subject's functional abilities while the wearable robotic system guarantees less support. Furthermore, the stability the exoskeleton addresses to the patient, allows a hands-free walking trial (with no clutches) which represents an integral part for a physiological locomotion restoration.
As gait involves both CNS and PNS, targeted rehabilitation must restore not only mechanics (speed, stride time and length) but also physiological gait pattern. This requires improvements at the level of both balance and lower limb joint motion. In this direction, wearable lower-limb powered exoskeletons promote functional training in a realistic walking-environment combined with a greater patient's engagement than in grounded devices. Human movement analysis quantitatively assesses the neuromuscular and biomechanical features of movement. Recent literature has highlighted the benefit of coupling GA and NMSM for treatment planning and supplementing this approach with robotic rehabilitation, however there is no study investigating gait effects from an OWET in those with PD, and no assessment that uses comprehensive GA and NMSM to reveal mechanistic changes as a result of therapy.
Neurophysiology of PD: A stalwart of PD research has been EEG, which is widely used to evaluate executive dysfunction while fMRI can detect cortical changes in motor activations during motor tasks. The protocol to use GA in combination with fMRI has already been adopted by the investigators in order to display the impacts of the rehabilitation process on the reorganization of the neural network, describing and quantifying the neural activity and the recovery after the treatment.
Motion analysis in PD: Gait in people with PD has been thoroughly studied with 3D GA systems in recent years, documenting a typical hypokinetic gait reduction of the stride-length with asymmetry between the strides, an increment of the cadence, the stance and double support phases, which compensates for the reduced stride length.
NMSM: Combining GA and NMSM enables one to track disease progression with enhanced precision. This has been demonstrated across a range of neuromuscular pathologies and healthy individuals. Critically, for each individual a neuromusculoskeletal model is created, driven by the individual's own EMG signals, and tracking their biomechanics, as has recently applied in neurologically impaired individuals. This creates a novel model that links in vivo neuromuscular functions to the individual, thus providing new biomarkers to assess and track PD motor impairment. Furthermore, since joint stiffness depends both on neural recruitment and mechanical properties, it is likely to provide a potent representation of neural and musculoskeletal PD impairment.
Significance and potential impact This project addresses the potential for OWET to restore normal gait in PD patients. OWET aims to improve overall body motion and lower joint stiffness in those with PD, thereby improving function, quality of life, and reducing risk of injurious falls. The proposed robotic device (Ekso GT™, EksoBionics, Richmond, CA, USA) relies functions by providing passive assistance to the ankle joint, which affects the rest of the body through mechanical coupling. Currently, the amount of device assistance is estimated based on a therapist experience and expertise. Modern motion analysis methods enable us to objectively assess the required assistance providing a means to tailor the assistance to each individual and remove the risks of clinical guesswork. Robotic devices assist the physical therapist by providing task-specific repeatable mechanical action to support therapies and enable higher intensity of training. OWET aims to reduce lower limb joint stiffness, which is a recognized biomarker of PD, thereby enhancing rehabilitation for PD patients.
Findings linked with the proposed study will likely give substantial solutions to the management of gait and postural disorders (posture, balance, and gait) in PD where valid interventions (pharmacological, neurosurgery, traditional physiotherapy) are lacking. Moreover, a NMSM that identifies patient-specific variables for therapy could be used to assess treatment outcomes but also to conduct on-line rehabilitation therapy by means remote control of the assistive device. This will provide a number of advantages over conventional approaches proposing an active treatment that is personalized and scalable to large populations and including a standardized training environment and an adaptable support that has the ability to increase the treatment intensity and dose, without being a burden on therapists. OWET is thus an ideal means to complete conventional therapy in clinic, while rehabilitation robots bear the potential for continued home therapy using simpler devices.
Study design The study will be carried out over 36 months. Patients with clinically established diagnosis of PD according to the U.K. Parkinson's Disease Society Brain Bank Diagnostic criteria will be recruited. The diagnosis will be reviewed by a neurologist specialized on movement disorders. Briefly, 50 patients with mild to moderate disease severity, will be enrolled according to the inclusion\exclusion criteria included in the dedicated section below.
The activities will be organized into 4 work packages (WP), each with measurable outputs verified by scheduled deliverables/milestones.
WP1: Clinical Trial. The sample size has been defined based on published data of gait velocity in PD subjects, and a target sample of fifty PD individuals (divided in two separate cohorts) has been selected to achieve a power of at least 80% for detecting a mean group differences in mean gait velocity (p = 0.05). One cohort (n=25) will undergo a multidisciplinary intensive rehabilitation treatment, and the other will be treated with OWET. At baseline (T0) subjects will undergo neurophysiological evaluation (EEG-fMRI) and GA. Participants will then undergo an 8-weeks OWET. After the therapy (T1), the subjects will be evaluated, with the same protocol as at T0. After another 2 months, a follow-up (T2) will be conducted using the same protocol as T0.
WP2: Motion analysis. State-of-the-art posture and GA will be performed pre- and post-rehabilitation.
WP3: NMSM. Using the data collected in WP1 and WP2, NMSM will be performed to obtain muscular force and joint stiffness. This NMSM will be used to assess PD neuromuscular function pre- and post-rehabilitation.
WP4: Neurophysiological assessment. A 256 channel High Density EEG (HD-EEG) recordings and analysis will be used to assess brain oscillation activity changes before and after the treatment. Multimodal brain imaging will be performed by simultaneous acquisition and analysis of neurophysiological signals (EEG/EMG) and fMRI data to assess the resting state connectivity and activation differences between pre- and post-treatment and to identify if the changes in the cortical activity is linked with the changes detected in WP3.
Anticipated Results Locomotor functions are positively recovered by a functional gait training. Indeed, in post-stroke subjects, patients who underwent this therapy have already shown to be more likely to achieve an independent walking than people who did not receive the same treatment.
OWET will improve quality of gait and balance. Effects with OWET will impact the quality of life. The results with OWET will provide innovative information for rehabilitative programs. The impact of the intervention will be assessed by measurable outcomes listed in the dedicated section below.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease
Keywords
Parkinson Disease, rehabilitation exhoskeleton, gait analysis, fMRI, Electroencephalogram
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
EksoGT
Arm Type
Experimental
Arm Description
Device: EksoGT. EksoGT is an overground wearable gait trainer. The therapy will be carried out 3 days a week for 4 weeks.
Arm Title
Functional kinematic training
Arm Type
Active Comparator
Arm Description
Device: No device. The functional kinematic training will be delivered as comparator treatment and will be carried out 3 days a week for 4 weeks.
Intervention Type
Device
Intervention Name(s)
Experimental: EksoGT
Intervention Description
EksoGT is an overground wearable gait trainer. The therapy will be carried out 3 days a week for 4 weeks.
Intervention Type
Other
Intervention Name(s)
Functional kinematic training
Intervention Description
Device: No device. The functional kinematic training will be delivered as comparator treatment and will be carried out 3 days a week for 4 weeks.
Primary Outcome Measure Information:
Title
Change in joint kinematics after 30 days
Description
Joint kinematics (degrees): trunk, pelvis, hip, knee, ankle (flexion-extension, ab-adduction, internal - external rotation)
Time Frame
Day 30
Title
Change in joint kinematics after 60 days
Description
Joint kinematics (degrees): trunk, pelvis, hip, knee, ankle (flexion-extension, ab-adduction, internal - external rotation)
Time Frame
Day 60
Title
Change in Spatiotemporal parameters after 30 days - Gait velocity
Description
Gait velocity (meters/seconds)
Time Frame
Day 30
Title
Change in Spatiotemporal parameters after 60 days - Gait velocity
Description
Gait velocity (meters/seconds)
Time Frame
Day 60
Title
Change in Spatial parameters after 30 days
Description
Step width (meters), step length (meters)
Time Frame
Day 30
Title
Change in Spatial parameters after 60 days
Description
Step width (meters), step length (meters)
Time Frame
Day 60
Title
Change in Temporal parameters after 30 days
Description
Step duration (seconds), gait period (seconds),stance period (seconds), swing period (seconds), double support (seconds)
Time Frame
Day 30
Title
Change in Temporal parameters after 60 days
Description
Step duration (seconds), gait period (seconds),stance period (seconds), swing period (seconds), double support (seconds)
Time Frame
Day 60
Title
Change in Spatiotemporal parameters after 30 days - Cadence
Description
Cadence (steps/minute)
Time Frame
Day 30
Title
Change in Spatiotemporal parameters after 60 days - Cadence
Description
Cadence (steps/minute)
Time Frame
Day 60
Title
Change in balance after 30 days - center of pressure spatial parameters
Description
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean distance from centre of COP trajectory (mm), root mean square of COP time series (mm), sway path, total COP trajectory length (mm), range of COP displacement (mm).
Time Frame
Day 30
Title
Change in balance after 60 days - center of pressure spatial parameters
Description
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean distance from centre of COP trajectory (mm), root mean square of COP time series (mm), sway path, total COP trajectory length (mm), range of COP displacement (mm)
Time Frame
Day 60
Title
Change in balance after 30 days - center of pressure velocity
Description
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean COP velocity (mm/s)
Time Frame
Day 30
Title
Change in balance after 60 days - center of pressure velocity
Description
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean COP velocity (mm/s)
Time Frame
Day 60
Title
Change in balance after 30 days - center of pressure frequency
Description
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean frequency (Hz), i.e., number, per second, of loops that have to be run by COP to cover total trajectory equal to sway path ; median frequency (Hz), frequency below which 50% of total power is present; 95% power frequency (Hz), frequency below which 95% of total power is present, centroidal frequency (Hz), frequency at which spectral mass is concentrated.
Time Frame
Day 30
Title
Change in balance after 60 days - center of pressure frequency
Description
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: mean frequency (Hz), i.e., number, per second, of loops that have to be run by COP to cover total trajectory equal to sway path ; median frequency (Hz), frequency below which 50% of total power is present; 95% power frequency (Hz), frequency below which 95% of total power is present, centroidal frequency (Hz), frequency at which spectral mass is concentrated.
Time Frame
Day 60
Title
Change in balance after 30 days - center of pressure ellipse parameters
Description
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: area of 95% confidence circumference (mm^2), area of 95% confidence ellipse (mm^2).
Time Frame
Day 30
Title
Change in balance after 60 days - center of pressure ellipse parameters
Description
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: area of 95% confidence circumference (mm^2), area of 95% confidence ellipse (mm^2).
Time Frame
Day 60
Title
Change in balance after 30 days - center of pressure sway area
Description
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: sway area, computed as area included in COP displacement per unit of time (mm^2/seconds).
Time Frame
Day 30
Title
Change in balance after 60 days - center of pressure sway area
Description
Balance during Romberg Test. From the center of pressure (COP) the following parameters will be extracted: sway area, computed as area included in COP displacement per unit of time (mm^2/seconds).
Time Frame
Day 60
Title
Change in muscle forces after 30 days
Description
Musculotendon forces estimated via musculoskeletal modeling (OpenSim, CEINMS)
Time Frame
Day 30
Title
Change in muscle forces after 60 days
Description
Musculotendon forces estimated via musculoskeletal modeling (OpenSim, CEINMS)
Time Frame
Day 60
Secondary Outcome Measure Information:
Title
Change in Movement Disorder Society - Unified Parkinson Disease Rating Scale (MDS-UPDRS) after 30 days
Description
MDS-UPDRS in all its four components (0 no disability - 199 total disability)
Time Frame
Day 30
Title
Change in Movement Disorder Society - Unified Parkinson Disease Rating Scale (MDS-UPDRS) after 60 days
Description
MDS-UPDRS in all its four components (0 no disability - 199 total disability)
Time Frame
Day 60
Title
Change in Timed Up and Go test (TUG) after 30 days
Description
Timed Up and Go test (TUG) (>= 12 seconds risk of falling).
Time Frame
Day 30
Title
Change in Timed Up and Go test (TUG) after 60 days
Description
Timed Up and Go test (TUG) (>= 12 seconds risk of falling).
Time Frame
Day 60
Title
Change in Berg Balance Scale (BBS) after 30 days
Description
Berg Balance Scale (BBS) (56 functional balance, < 45 greater risk of falling).
Time Frame
Day 30
Title
Change in Berg Balance Scale (BBS) after 60 days
Description
Berg Balance Scale (BBS) (56 functional balance, < 45 greater risk of falling).
Time Frame
Day 60
Title
Change in Falls Efficacy Scale (FES) after 30 days
Description
Falls Efficacy Scale (FES) (16 severe concern about falling - 64 no concern about falling).
Time Frame
Day 30
Title
Change in Falls Efficacy Scale (FES) after 60 days
Description
Falls Efficacy Scale (FES) (16 severe concern about falling - 64 no concern about falling).
Time Frame
Day 60
Title
Change in 6 minutes walking test (6-WT) after 30 days
Description
6 minutes walking test (6-WT) (min 311 meters - max 673 meters)
Time Frame
Day 30
Title
Change in 6 minutes walking test (6-WT) after 60 days
Description
6 minutes walking test (6-WT) (min 311 meters - max 673 meters)
Time Frame
Day 60
Title
Change in Ziegler Protocol for the assessment of Freezing of Gait (FOG) severity after 30 days
Description
Ziegler Protocol for the assessment of FOG severity (0 no festination, no FOG - 1 festination - 2 FOG).
Time Frame
Day 30
Title
Change in Ziegler Protocol for the assessment of Freezing of Gait (FOG) severity after 60 days
Description
Ziegler Protocol for the assessment of FOG severity (0 no festination, no FOG - 1 festination - 2 FOG).
Time Frame
Day 60
Title
Change The New Freezing of Gait Questionnaire (N-FOGQ) severity after 30 days
Description
The New Freezing of Gait Questionnaire (N-FOGQ) (0 never happened, 4 unable to walk for more than 30s).
Time Frame
Day 30
Title
Change The New Freezing of Gait Questionnaire (N-FOGQ) severity after 60 days
Description
The New Freezing of Gait Questionnaire (N-FOGQ) (0 never happened, 4 unable to walk for more than 30s).
Time Frame
Day 60
Title
Change in neurophysiological assessment after 30 days : electromyography (EMG)
Description
Magnitude (milliVolt)
Time Frame
Day 30
Title
Change in neurophysiological assessment after 60 days : electromyography (EMG)
Description
Magnitude (milliVolt)
Time Frame
Day 60
Title
Change in neurophysiological assessment after 30 days : electroencephalogram (EEG)
Description
Spectral parameters (Hz)
Time Frame
Day 30
Title
Change in neurophysiological assessment after 60 days : electroencephalogram (EEG)
Description
Spectral parameters (Hz)
Time Frame
Day 60
Title
Change in neurophysiological assessment after 30 days : functional Magnetic Resonance Imaging (fMRI)
Description
Number of active voxel in the region of interest
Time Frame
Day 30
Title
Change in neurophysiological assessment after 60 days : functional Magnetic Resonance Imaging (fMRI)
Description
Number of active voxel in the region of interest
Time Frame
Day 60
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient with rigid-acinetic bilateral PD form
Hoehn-Yahr between 3-4
At least 4 years of disease history
Stable drug therapy response without any change performed in the 3 months before the study
Presence of freezing (FOG) and of postural instability not responding to parkinsonian therapy
Mini Mental State Evaluation > 24/30
Exclusion Criteria:
Systemic illness
Presence of cardiac pacemaker
Postural abnormalities, orthopedic comorbidities that do not match the active physiotherapy treatment
Presence of deep brain stimulation
Presence of severe disautonomia with marked hypotension
Obsessive-Compulsive disorder (OCD)
Major depression
Dementia and psychosis
History or active neoplasia
Pregnancy
Other criteria that do not respect the device counterindications
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zimi Sawacha, PhD
Phone
+39 0498277633
Email
zimi.sawacha@dei.unipd.it
First Name & Middle Initial & Last Name or Official Title & Degree
Marco Romanato, MSEng
Phone
+39 0498277805
Email
romanato@dei.unipd.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zimi Sawacha, PhD
Organizational Affiliation
University of Padova
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Padova
City
Padova
ZIP/Postal Code
35128
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
zimi sawacha, PhD
Phone
+39 0498277633
Email
zimi.sawacha@dei.unipd.it
First Name & Middle Initial & Last Name & Degree
marco romanato, MSEng
Phone
+39 0498277805
Email
romanato@dei.unipd.it
Facility Name
Fresco Parkinson Center, Villa Margherita
City
Vicenza
ZIP/Postal Code
36057
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Daniele Volpe, MD
Email
daniele.volpe@casadicuravillamargherita.it
12. IPD Sharing Statement
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Links:
URL
https://doi.org/10.1186/s12984-016-0162-5
Description
Dennis R. Louie, Powered robotic exoskeletons in post-stroke rehabilitation of gait: a scoping review
URL
http://doi.org/10.3390/app9142868
Description
A De Luca, Exoskeleton for Gait Rehabilitation: Effects of Assistance, Mechanical Structure, and Walking Aids on Muscle Activations
Learn more about this trial
Quantitative Assessment of Training Effects Using EKSOGT Exoskeleton in Quantitative Assessment of Training Effects Using EKSOGT Exoskeleton in Parkinson Disease Patients
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