Sensor-based Assessment and Rehabilitation of Balance in Neurological Diseases (BALANCE)
Primary Purpose
Stroke, Multiple Sclerosis, Parkinson Disease
Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Experimental Group
Control Group
Sponsored by
About this trial
This is an interventional treatment trial for Stroke focused on measuring Balance, Sensor-based rehabilitation, Virtual Reality
Eligibility Criteria
Inclusion Criteria:
Common criteria:
- Berg Balance Scale < 50/56;
- Ability to maintain the standing position with o without one support for 1 minute;
- Functional Independence measure < 100/126;
- Barthel Index < 80/100.
Stroke:
- Single ischemic stroke;
- Lesion occured after 2 and within 18 months;
- National Institute of Health Stroke Scale ≤ 14.
Parkinson:
- 1.5 < Hoehn & Yahr < 3;
- Subitem "freezing when walking"of the UPDRS ≤ 2.
Multiple Sclerosis:
- Relapsing remitting or secondary progressive Multiple Sclerosis;
- Expanded Disability Status Scale ≤ 6.5.
Exclusion Criteria:
- Untreated epilepsy;
- Major depressive disorder;
- Fractures;
- Dementia;
- Ideomotor Apraxia;
- Neglect;
- Severe impairment of verbal comprehension;
- Severe acoustic and visual disorders.
Sites / Locations
- IRCCS Fondazione MondinoRecruiting
- IRCCS ICS Maugeri Spa SBRecruiting
- IRCCS San Raffaele PisanaRecruiting
- IRCCS Fondazione Santa LuciaRecruiting
- San Camillo IRCCSRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Experimental Group (EG)
Control Group (CG)
Arm Description
In the EG the subjects will perform balance exercises using the OAK system under the supervision of a trained physiotherapist. The treatment will last 3 weeks with daily sessions of 60 minutes, 5 times per week.
In the CG the subjects will be asked to perform conventional balance exercises under the supervision of a physiotherapist. The treatment will last 3 weeks with daily sessions of 60 minutes, 5 times per week.
Outcomes
Primary Outcome Measures
Berg Balance Scale (BBS)
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means better outcome (minimum score = 0, maximum score = 56).
Secondary Outcome Measures
Number of falls during the last year
Applied at the beginning and at the end of treatment (after 15 sessions).
Functional Ambulation Classification (FAC)
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means better outcome (minimum score = 0, maximum score = 5).
Activities specific-Balance Confidence scale (ABC)
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means better outcome (minimum score = 0, maximum score = 100).
Functional Independence Measure (FIM)
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means better outcome (minimum score = 0, maximum score = 126).
Barthel Index (BI)
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means better outcome (minimum score = 0, maximum score = 100).
National Institution of Health Stroke Scale (NIHSS)
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means worse outcome (minimum score = 0, maximum score = 42).
Unified Parkinson's Disease Rating Scale (UPDRS)
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means worse outcome (minimum score = 0, maximum score = 147).
Hoehn & Yahr Scale (H&Y)
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means worse outcome (minimum score = 0, maximum score = 5).
Kurtzke Extended Disability Status Scale (EDSS)
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means worse outcome (minimum score = 0, maximum score = 10).
Full Information
NCT ID
NCT04874051
First Posted
April 30, 2021
Last Updated
March 20, 2023
Sponsor
IRCCS San Camillo, Venezia, Italy
Collaborators
IRCCS San Raffaele, Istituti Clinici Scientifici Maugeri SpA, IRCCS National Neurological Institute "C. Mondino" Foundation, I.R.C.C.S. Fondazione Santa Lucia
1. Study Identification
Unique Protocol Identification Number
NCT04874051
Brief Title
Sensor-based Assessment and Rehabilitation of Balance in Neurological Diseases
Acronym
BALANCE
Official Title
Sensor-Based Analysis And rehabiLitation of bAlance in Neurological Diseases: a multiCentric randomizEd Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 2, 2019 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
IRCCS San Camillo, Venezia, Italy
Collaborators
IRCCS San Raffaele, Istituti Clinici Scientifici Maugeri SpA, IRCCS National Neurological Institute "C. Mondino" Foundation, I.R.C.C.S. Fondazione Santa Lucia
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Balance impairment is one of the most common disorders due to a neurological diseases. Sensor-based technologies may be useful for falls prevention and balance recovery during patients hospitalization. OAK Elderly Care System (Khymeia Group, Noventa Padovana, Italy) allows the assessment of fall risk, the centre of pressure and the execution of balance exercises in a virtual environment.
Detailed Description
The aim of the study is to compare the therapy provided by means of the OAK Elderly Care System with conventional physiotherapy for balance rehabilitation in patients affected by stroke, Multiple Sclerosis (MS) and Parkinson Disease (PD).
OAK Elderly Care System consists of two independent balance boards and three sensors for the kinematic tracking of the trunk and lower limbs. These components allow the assessment of the centre of pressure and the execution of exercises in a virtual environment.
120 patients (40 stroke, 40 MS, 40 PK) hospitalized at 4 different italian hospitals, were enrolled according to inclusion and exclusion criteria and randomly assigned to two groups (i.e. intervention group, control group). Intervention group received 1 daily hour of technology-based treatment, while the control group underwent 1 daily hour of physiotherapy for balance rehabilitation, in addiction to 1 hour of conventional physiotherapy. Both treatments lasted 15 sessions. Before and after treatment balance, walking, daily living autonomy and pathology-specific features were assessed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Multiple Sclerosis, Parkinson Disease
Keywords
Balance, Sensor-based rehabilitation, Virtual Reality
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The experimental group is treated through a sensor-based devices in a virtual environment, while the control group is treated through conventional physiotherapy for balance rehabilitation
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental Group (EG)
Arm Type
Experimental
Arm Description
In the EG the subjects will perform balance exercises using the OAK system under the supervision of a trained physiotherapist. The treatment will last 3 weeks with daily sessions of 60 minutes, 5 times per week.
Arm Title
Control Group (CG)
Arm Type
Active Comparator
Arm Description
In the CG the subjects will be asked to perform conventional balance exercises under the supervision of a physiotherapist. The treatment will last 3 weeks with daily sessions of 60 minutes, 5 times per week.
Intervention Type
Device
Intervention Name(s)
Experimental Group
Intervention Description
The experimental treatment will be provided by means of the OAK system. This device consists of 1 cabinet with 2 independent balance boards, 2 monitors (one for the physiotherapist and one for the patient) and 3 wireless IMUs (one for the left lower limb, one for the right lower limb and one for the trunk). The 2 balance boards provide body weight transfer exercises, while the wireless motion sensors provide one leg stance exercises or trunk exercises in a virtual environment.
Intervention Type
Other
Intervention Name(s)
Control Group
Intervention Description
The Control Group will perform conventional balance exercises similar to the exercises provided with the OAK system.
Primary Outcome Measure Information:
Title
Berg Balance Scale (BBS)
Description
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means better outcome (minimum score = 0, maximum score = 56).
Time Frame
Change from baseline Berg Balance Scale at the end of the therapy (three weeks thereafter)
Secondary Outcome Measure Information:
Title
Number of falls during the last year
Description
Applied at the beginning and at the end of treatment (after 15 sessions).
Time Frame
Change from baseline number of falls during the last year scale at the end of the therapy (three weeks thereafter)
Title
Functional Ambulation Classification (FAC)
Description
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means better outcome (minimum score = 0, maximum score = 5).
Time Frame
Change from baseline Functional Ambulation Classification at the end of the therapy (three weeks thereafter)
Title
Activities specific-Balance Confidence scale (ABC)
Description
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means better outcome (minimum score = 0, maximum score = 100).
Time Frame
Change from baseline Activities specific-Balance Confidence scale at the end of the therapy (three weeks thereafter)
Title
Functional Independence Measure (FIM)
Description
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means better outcome (minimum score = 0, maximum score = 126).
Time Frame
Change from baseline Functional Independence Measure at the end of the therapy (three weeks thereafter)
Title
Barthel Index (BI)
Description
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means better outcome (minimum score = 0, maximum score = 100).
Time Frame
Change from baseline Barthel Index at the end of the therapy (three weeks thereafter)
Title
National Institution of Health Stroke Scale (NIHSS)
Description
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means worse outcome (minimum score = 0, maximum score = 42).
Time Frame
Change from baseline National Institute of Health Stroke Scale at the end of the therapy (three weeks thereafter)
Title
Unified Parkinson's Disease Rating Scale (UPDRS)
Description
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means worse outcome (minimum score = 0, maximum score = 147).
Time Frame
Change from baseline Unified Parkinson's Disease Rating Scale at the end of the therapy (three weeks thereafter)
Title
Hoehn & Yahr Scale (H&Y)
Description
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means worse outcome (minimum score = 0, maximum score = 5).
Time Frame
Change from baseline Hoehn & Yahr Scale at the end of the therapy (three weeks thereafter)
Title
Kurtzke Extended Disability Status Scale (EDSS)
Description
Applied at the beginning and at the end of treatment (after 15 sessions). A higher score means worse outcome (minimum score = 0, maximum score = 10).
Time Frame
Change from baseline Kurtzke Extended Disability Status Scale at the end of the therapy (three weeks thereafter)
Other Pre-specified Outcome Measures:
Title
Instrumental assessment
Description
The OAK system will record the changes of the center of pressure during 30 seconds, with relaxed arms and eyes open.
Time Frame
Change from baseline BBS at the end of the therapy (three weeks thereafter)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Common criteria:
Berg Balance Scale < 50/56;
Ability to maintain the standing position with o without one support for 1 minute;
Functional Independence measure < 100/126;
Barthel Index < 80/100.
Stroke:
Single ischemic stroke;
Lesion occured after 2 and within 18 months;
National Institute of Health Stroke Scale ≤ 14.
Parkinson:
1.5 < Hoehn & Yahr < 3;
Subitem "freezing when walking"of the UPDRS ≤ 2.
Multiple Sclerosis:
Relapsing remitting or secondary progressive Multiple Sclerosis;
Expanded Disability Status Scale ≤ 6.5.
Exclusion Criteria:
Untreated epilepsy;
Major depressive disorder;
Fractures;
Dementia;
Ideomotor Apraxia;
Neglect;
Severe impairment of verbal comprehension;
Severe acoustic and visual disorders.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Andrea Turolla, PhD
Phone
00390412207
Ext
531
Email
andrea.turolla@ospedalesancamillo.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrea Turolla, PhD
Organizational Affiliation
San Camillo IRCCS
Official's Role
Principal Investigator
Facility Information:
Facility Name
IRCCS Fondazione Mondino
City
Pavia
ZIP/Postal Code
27100
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cristina Tassorelli, Prof.
Phone
0382380425
Email
cristina.tassorelli@unipv.it
First Name & Middle Initial & Last Name & Degree
Roberto De Icco
Facility Name
IRCCS ICS Maugeri Spa SB
City
Pavia
ZIP/Postal Code
27100
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Giorgio Maggioni, Dr.
Phone
0322884711
Email
giorgio.maggioni@icsmaugeri.it
Facility Name
IRCCS San Raffaele Pisana
City
Rom
ZIP/Postal Code
00163
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marco Franceschini, Dr.
Email
marco.franceschini@sanraffaele.it
Phone
06660581
First Name & Middle Initial & Last Name & Degree
Michela Goffredo
Facility Name
IRCCS Fondazione Santa Lucia
City
Rom
ZIP/Postal Code
00179
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Giovanni Morone, Dr.
Email
g.morone@hsantalucia.it
Facility Name
San Camillo IRCCS
City
Venice
ZIP/Postal Code
30126
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Francesca Baldan
First Name & Middle Initial & Last Name & Degree
Sara Federico
First Name & Middle Initial & Last Name & Degree
Martina Pavanetto
12. IPD Sharing Statement
Learn more about this trial
Sensor-based Assessment and Rehabilitation of Balance in Neurological Diseases
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