PURO - PUlmonary Rehabilitation With O-RAGT Platform

Stroke Clinical Trial

— PURO  

Official title:

Metabolic Consumption, Cardiorespiratory Effort, Cardiac Autonomic Control and Fatigability During Exoskeleton-assisted (the U&O Suite) sit-to Stand Maneuver and Walking in People With Neurological Diseases With Moderate to Severe Gait Disability.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05757830
• Other study ID #: 825003
• Status: Completed
• Phase: N/A
• Start date: December 23, 2022
• Est. completion date: March 31, 2023

Study information

• Verified date: January 2023
• Source: Fondazione Don Carlo Gnocchi Onlus
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this interventional study is to assess differences in the metabolic consumption, the cardiorespiratory effort, the cardiac autonomic adaptation, and fatigability during ADL, such as standing from a chair and walking while wearing an electrically powered exoskeleton in different modes of supports in subjects with neurological diseases with moderate to severe walking impairments.

Description:

In people with severe gait impairments due to neurological diseases walk recovery is one primary goal, since achieving independent ambulation is a major contributing factor to their quality of life. Beyond walking, other very common Activities of Daily Living (ADL), such as postural transitions (which requires an integrity of the autonomic control mechanisms of blood pressure) and stair climbing (which requires the necessary strength in the lower limbs to lift one's own body weight) should be guaranteed by any rehabilitative intervention. Although physiotherapy treatments have proven effectiveness in improving gait and balance, conventional overground walking training may be very difficult or even impossible for patients with moderate to severe gait problems and limited cardiovascular capacity due to a too high energy demand (exercise intensity) (Calabrò 2022). Wearable powered exoskeletons could be used to provide overground robotic assisted gait training (RAGT). Indeed, RAGT has shown clinically significant improvements in gait and balance outcomes and could be considered a valid approach to enhance gait function in people with severe gait impairments due to neurological diseases(Bowman 2021). Little is known about the impact of robotic training on cardiovascular parameters and the metabolic / energy cost of walking with a wearable powered exoskeleton compared to unassisted overground walking in population with neurological diseases. It is possible that exoskeletons allow walking while keeping cardiorespiratory effort under control with a lower metabolic cost. Moreover, people with severe gait impairments can suffer from disturbed cardiac autonomic control during exercise which affects exercise tolerance and balance during orthostatic challenges, such as the sit-to-stand maneuver. Indeed, to recommend RAGT in people with neurological diseases with moderate to severe gait impairments, the impact of the cardiac autonomic tone on sit-to-standing and walking with an exoskeleton should be investigated. The use of an assisted as needed exoskeleton in clinical practice with population with moderate-severe neurological disabilities could increase their locomotor function by reducing the impact on metabolic consumption and cardiorespiratory effort compared to conventional overground walking training without an exoskeleton. Moreover, cardiovascular autonomic dysfunction (CAD), if any, should not be worsened by walking with an exoskeleton compared to conventional overground walking training, and should not constitute an impediment in the adaptation of the cardiovascular adaptation (especially of blood pressure) to the postural transitions. The goal of this interventional study is to assess differences in the metabolic consumption, the cardiorespiratory effort, the cardiac autonomic adaptation, and fatigability during ADL, such as standing from a chair and walking while wearing an electrically powered exoskeleton in different modes of supports in subjects with neurological diseases with moderate to severe walking impairments.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: March 31, 2023
• Est. primary completion date: March 31, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• Able to perform 4 minutes of back-and-forth locomotion with assistance or resting periods;
• Height between 160 and 195 cm;
• Weight not exceeding 100 kg;
• Diagnosis of Multiple Sclerosis with moderate to severe disability (5,5 < EDSS < 8,0);
• Diagnosis of stroke or traumatic brain damage (1 = FAC = 3);
• Diagnosis of spinal cord injury with neurological level of injury<T2 (3 = WISCI II = 16) with a Asia Impairment Score B, C or D.
• Able to perform 4 minutes of back-and-forth locomotion with assistance or resting periods;
• Able to use walker;

Exclusion Criteria:

• Impairments in the upper limbs that do not allow the user to hold the crutches/walker.
• Skin injuries in the areas where the exoskeleton is in contact with the user.
• Fractures not solved or bone pathologies in lower limbs in which the use of the exoskeleton could be risky (advanced osteoporosis).
• Psychiatric or cognitive problems that can interfere with the correct use of the device.
• Important muscle/joint retractions in lower limbs (Modified Ashworth Scale > 3).
• Any medical conditions that could interfere with the autonomic cardiovascular control (e.g severe diabetes).
• Use of beta blocker drugs.
• Presence of severe cardiovascular diseases.

Related Conditions & MeSH terms

• Brain Injuries
• Brain Injuries, Traumatic
• Multiple Sclerosis
• Spinal Cord Injuries
• Spinal Cord Injury
• Stroke
• Traumatic Brain Damage

Intervention

Device:
• UANGO suite exoskeleton
Each subject will perform 3 experimental conditions (Condition 1: Walking without exoskeleton; Condition 2: Walking with exoskeleton; Condition 3: Walking with exoskeleton and walker). Each condition includes 5 triasl (Trial 1 - Sitting: 5 minutes, sitting at rest in comfortable position; Trial 2 - Standing: 5 minutes, with assistance; Trial 3 - Comfortable speed Walking (100% assisted): 4 min during back-and-forth locomotion on a 20-m length linear flat path; Trial 4 - Comfortable speed Walking (75% assistance): 4 min during back-and-forth locomotion on a 20-m length linear flat path, Trial 4 is not available in condition 1; Trial 5 - 1 minute Sit to stand test). Nasa TLX and RPE will be requested at the end of each trial. Usability questionnaires will be fullfilled at the end of condition 2 and condition 3.

Locations

Country	Name	City	State
Italy	Fondazione Don Carlo Gnocchi	Milan	MI
Lithuania	Lithuanian University of Health Sciences	Kaunas
Netherlands	Roessingh Research and Development	Enschede	AH
Spain	Hospital Nacional de Parapléjicos de Toledo	Toledo

Sponsors (4)

Lead Sponsor	Collaborator
Fondazione Don Carlo Gnocchi Onlus	Hospital Nacional de Parapléjicos de Toledo, Lithuanian University of Health Sciences, Roessingh Research and Development

Countries where clinical trial is conducted

Italy,  Lithuania,  Netherlands,  Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Walking meters change during 4 minute walking test	4 minutes walking test on a 20-meter corridor	Baseline (Condition 1) and after 24 hours (Condition 2) and after 48 hours (Condition 3)
Secondary	Number of repetitions change in one-minute sit to stand test	The one-minute sit to stand test is performed with a chair of standard height without arm rests. The patient is ensured to be seated upright on the chair. The patient sat with the knees and hips flexed to 90°, feet placed flat on the floor hip-width apart, and the hands placed on the hips. Every get up from one's chair was validated to check if complete sit-to-stand-to-sit sequence was achieved.	Baseline (Condition 1) and after 24 hours (Condition 2) and after 48 hours (Condition 3)
Secondary	Average VO2 change during 4 minute walking test	Metabolic-related variables measured with K5-Cosmed device during 4 minute walking test on a 20-meter corridor	Baseline (Condition 1) and after 24 hours (Condition 2) and after 48 hours (Condition 3)
Secondary	O2 cost of walking change during 4 minute walking test	Metabolic-related variables measured with K5-Cosmed device during 4 minute walking test on a 20-meter corridor	Baseline (Condition 1) and after 24 hours (Condition 2) and after 48 hours (Condition 3)
Secondary	Net metabolic power change during 4 minute walking test	Metabolic-related variables measured with K5-Cosmed device during 4 minute walking test on a 20-meter corridor	Baseline (Condition 1) and after 24 hours (Condition 2) and after 48 hours (Condition 3)
Secondary	Physiological cost index (PCI) change during 4 minute walking test	Metabolic-related variables measured with PCI scale during 4 minute walking test on a 20-meter corridor	Baseline (Condition 1) and after 24 hours (Condition 2) and after 48 hours (Condition 3)
Secondary	Average heart rate change during 4 minute walking test	Cardiorespiratory parameters measured with pulse oximeter device during 4 minute walking test on a 20-meter corridor	Baseline (Condition 1) and after 24 hours (Condition 2) and after 48 hours (Condition 3)
Secondary	Heart rate increase change during 4 minute walking test	Cardiorespiratory parameters measured with pulse oximeter device during 4 minute walking test on a 20-meter corridor	Baseline (Condition 1) and after 24 hours (Condition 2) and after 48 hours (Condition 3)
Secondary	Rating of perceived exertion of lower limbs change before and after each trials	Fatigue-related parameters using the Borg scale scoring system ranging from 6 to 20, where 6 means "no exertion at all" and 20 means "maximal exertion".	Baseline (Condition 1) and after 24 hours (Condition 2) and after 48 hours (Condition 3)
Secondary	Rating of perceived exertion of breath change before and after each trials	Fatigue-related parameters using the Borg scale scoring system ranging from 6 to 20, where 6 means "no exertion at all" and 20 means "maximal exertion".	Baseline (Condition 1) and after 24 hours (Condition 2) and after 48 hours (Condition 3)
Secondary	Assessment of device usability at the end of each condition	Usability will be assessed with the System Usability Scale (SUS). SUS consists of a 10 item questionnaire with five response options for respondents; from "strongly agree" to "strongly disagree".	Baseline (Condition 2) and after 24 hours (Condition 3)
Secondary	Assessment of users satisfaction at the end of each condition	Satisfaction will be assessed with Telehealth satisfaction questionnaire (TSQWT). The TSQWT contains six subscales evaluating the benefit, usability, self-concept, privacy and loss of control, quality of life and wearing comfort of the system. Each subscale includes five questions rated on a 5-point Likert scale between 0 (I strongly disagree) and 4 (I strongly agree). The total score ranges between 0 (no satisfaction) and 120 (extreme satisfaction).	Baseline (Condition 2) and after 24 hours (Condition 3)
Secondary	Assessment of the work load change during each trials	Task load will be assessed with Nasa Task Load Index. NASA (TLX) method assesses work load on five 7-point scales. Increments of high, medium and low.	Baseline (Condition 1) and after 24 hours (Condition 2) and after 48 hours (Condition 3)