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Neuroimaging Biomarkers Toward a Personalized Upper Limb Action Observation Treatment in Chronic Stroke Patients (BE-TOP)

Primary Purpose

Chronic Stroke

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Action Observation Treatrment
Observation of videos with Non Motor contents
Sponsored by
IRCCS San Raffaele
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Stroke focused on measuring Prevention and treatment of movement, Motor Function, Action Observation Therapy, Mirror Neuron System, Upper Limb Rehabilitation

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • chronic stroke (never experienced AOT);
  • first-ever unilateral stroke due to ischemia provoking a clinically evident upper limb/hand deficit;
  • diagnosis verified by brain imaging (MRI);
  • cognitive function sufficient to understand the experimental instructions
  • Chedoke-McMaster stroke Assessment Scale score greater than 1;
  • informed written consent to participate in the study.

Exclusion Criteria:

  • bilateral impairment,
  • severe sensory deficits in the paretic upper limb,
  • cognitive impairment or behavioral dysfunction,
  • refusal or inability to provide informed consent and
  • other current severe medical problems.

Sites / Locations

  • Casa di Cura del Policlinico di Milano
  • IRCCS San Raffaele PisanaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental Group (EG)

Control Group (CG)

Arm Description

The Experimental Group (EG) will observe and execute/repeat Activities of Daily Living (ADL) actions.

The COntrol Group (CG) will observe landscapes and perform the same actions observed by their peers but after verbal instructions.

Outcomes

Primary Outcome Measures

Change in Fugl-Meyer (FM) Test
The Fugl-Meyer Assessment (FMA) is a stroke-specific, performance-based impairment index. It is designed to assess motor functioning, balance, sensation and joint functioning in patients with post-stroke hemiplegia. It is applied clinically and in research to determine disease severity, describe motor recovery, and to plan and assess treatment. The scale is comprised of five domains and there are 155 items in total: Motor functioning (the score ranges from 0 (hemiplegia) to 100 points (normal motor performance). Divided into 66 points for upper extremity and 34 points for the lower extremity. Sensory functioning (from 0 to 24 points) Balance (from 0 to 14) Joint range of motion (from 0 to 44) Joint pain (from 0 to 44 ) Scale items are scored on the basis of ability to complete the item using a 3-point ordinal scale where 0=cannot perform, 1=performs partially and 2=performs fully. The total possible scale score is 226.

Secondary Outcome Measures

Change in Frenchay Arm Test (FAT)
The Frenchay Arm Test (FAT) is a measure of upper extremity proximal motor control and dexterity during ADL performance in patients with impairments resulting from neurological conditions. The FAT is an upper extremity specific measure of activity limitation.

Full Information

First Posted
July 31, 2019
Last Updated
August 2, 2022
Sponsor
IRCCS San Raffaele
Collaborators
Casa di Cura del Policlinico di Milano
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1. Study Identification

Unique Protocol Identification Number
NCT04047134
Brief Title
Neuroimaging Biomarkers Toward a Personalized Upper Limb Action Observation Treatment in Chronic Stroke Patients
Acronym
BE-TOP
Official Title
Neuroimaging Biomarkers Toward an Optimized and Personalized Action Observation Treatment in Chronic Stroke Patients: New Strategies to Maximize the Efficacy of Upper Limb Functional Rehabilitation.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2019 (Actual)
Primary Completion Date
November 30, 2022 (Anticipated)
Study Completion Date
January 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IRCCS San Raffaele
Collaborators
Casa di Cura del Policlinico di Milano

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
Much recent interest was raised by the use of Action Observation Treatment (AOT) in stroke patients rehabilitation. AOT, well-grounded in neurophysiology, is an updated approach, based on mirror neuron system (MNS) used to rebuild motor function despite injuries by engaging the brain regions active during action execution in individuals with limited mobility. This project aims at identifying, for the first time in Italy, neurophysiological electroencephalographic (EEG) biomarkers able to predict rehabilitation outcomes and providing an innovative optimized AOT rehabilitation protocol for chronic Stroke outpatients. EEG will be recorded to identify the most effective stimuli, quantify changes/recovery, profile patients. Moreover, an innovative AOT home-based program will be implemented. The translational research results will ensure advances in the optimization and personalization of the rehabilitative process thus contributing to improve the quality of life of chronic stroke patients. Stroke is a leading cause of death and one of the greatest causes of long-term disability that interferes with a good quality of life. Nowadays the rehabilitation interventions are the major component of patient's care to achieve functional outcome. In the last few years, in order to improve Activity of Daily Living (ADL), new noninvasive strategies have emerged as rehabilitative treatments rather than traditional physical therapies. The Action Observation Treatment (AOT), supported by results collected through randomized controlled trials, is one of these. This new rehabilitation approach is based on the properties of the Mirror Neuron System (MNS; 11-13). The extensive research of the last 20 years on the human MNS (hMNS) showed its importance not only in action recognition but also in motor intentions and other social cognitive functions. Lastly, because recruited also in damage brain (18,19), the MNS is demonstrated to provide satisfactory rehabilitative outcomes. The AOT takes advantage of the opportunity to restore functions despite the patient's impairment and it seems to be a valid example of translational medicine from basic neuroscience to rehabilitation. To date, neurophysiological outcomes were never used for translational purposes aimed to the optimization of the therapy and no evidence, in Italy, related to the effectiveness of the home-based program were proposed.
Detailed Description
This study protocol provides 3 experimental designs to satisfy 3 different specific aims as follows. Experimental design aim 1: To assess which kind of ADL visual stimuli will be most effective inducing motor excitability during action observation, EEG recording will be performed. 20 Stroke patients (10 with right lesion and 10 left one) will be recruited and video of feeding, self care and external actions showed. The EEG biomarkers will be identify. A comparison on EEG rhythm and biomarkers between the two groups and the ADL categories observed will be investigated. The most effective category will be subsequently selected for the Randomized Controlled Trial (RCT). Experimental design aim 2: This is an RCT study aimed to deeply investigate if EEG biomarkers are predictive of effectiveness of AOT on 40 Chronic Stroke outpatients in order to confirm the translational power of the optimized treatment. The subjects accurately enrolled for hospital program, will be randomly assigned to the Experimental Group (EG) or to the Control one (CG). The EG will observe and execute ADL actions, the CG will observe landscapes and perform the same actions observed by the others one but after verbal instructions. For each condition the patient will be presented with only 1 typology of motor task per day, starting from the easiest and ending with the most complex action throughout 15 sessions spread on 5 weeks (3 sessions/week). Tasks will be based on some relevant activities of daily living belonging to at least one between feeding, self-care or external actions category on the affected side. Each session will last about 15 minutes and will be repeated twice a day, at least 60 minutes apart. Before, after and in the middle of the treatment sessions all patients will be clinically, neurophysiologically (EEG and EMG) and behaviorally (Kinematics) assessed to verify neural plasticity and motor recovery. The follow-up at 2 months later will be carried out to assess retention of effects. Experimental design aim 3: The health policy to develop appropriate home-based rehabilitation programs for chronic stroke patients (24,25) could induce to explore whether AOT can meet the necessary translational requirements also for this type of care. A New group of 20 chronic stroke patients will be recruited and randomly assigned to the EG OR CG to follow the optimized AOT rehabilitation programs. After appropriate training of patients and caregivers, the use of tablets will let the home-based treatment. The investigators will define a low-cost highly accessible system based on tablet consumer technology for facilitating the AOT. In particular a tablet will be proposed with a web-based program that will be used to train the patients and receive a feedback of their progress. The whole treatment period will last 6 weeks. The focus of this evaluation will be on the feasibility of the home-based treatment and the usability of the platform as well as the subjects satisfaction with the services. A preliminary estimate of the recovery and overall improvement of functional performances of participants will also be provided with respect to clinical outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Stroke
Keywords
Prevention and treatment of movement, Motor Function, Action Observation Therapy, Mirror Neuron System, Upper Limb Rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental Group (EG)
Arm Type
Experimental
Arm Description
The Experimental Group (EG) will observe and execute/repeat Activities of Daily Living (ADL) actions.
Arm Title
Control Group (CG)
Arm Type
Active Comparator
Arm Description
The COntrol Group (CG) will observe landscapes and perform the same actions observed by their peers but after verbal instructions.
Intervention Type
Other
Intervention Name(s)
Action Observation Treatrment
Other Intervention Name(s)
AOT
Intervention Description
Participants will be asked to carefully observe the videos showing different daily actions. Each action will consist of 3 to 4 constituent motor acts. Each motor act will be presented for 3 minutes, totally lasting 12 min/video. At the end of each motor act presentation, participants will be asked to execute with the affected hand the observed motor sequence for 2 minutes (20 minutes/session). 10 daily actions will be recorded. Each video will be presented to participants twice a day, in order to complexity as judged by the experimenter. Only 1 typology of motor task per day for each condition, starting from the easiest and ending with the most complex action throughout 15 sessions spread on 5 weeks (3 sessions/week). Tasks will be based on some relevant activities of daily living belonging to at least one between feeding, self-care or external actions category on the affected side. Each session will last about 15 minutes and will be repeated twice a day, at least 60 minutes apart.
Intervention Type
Other
Intervention Name(s)
Observation of videos with Non Motor contents
Other Intervention Name(s)
NMO
Intervention Description
Participants will be asked to observe video clips with no specific motor content. Videos will concern scientific, geographical and historical issues. As for cases, video clips will be divided into three to four parts. At the end of each part, controls will execute the same actions as cases, in the same order. In this way cases and controls will undergo the same amount of motor practice and receive the same amount of visual stimulation, the only difference being the content of visual stimuli.
Primary Outcome Measure Information:
Title
Change in Fugl-Meyer (FM) Test
Description
The Fugl-Meyer Assessment (FMA) is a stroke-specific, performance-based impairment index. It is designed to assess motor functioning, balance, sensation and joint functioning in patients with post-stroke hemiplegia. It is applied clinically and in research to determine disease severity, describe motor recovery, and to plan and assess treatment. The scale is comprised of five domains and there are 155 items in total: Motor functioning (the score ranges from 0 (hemiplegia) to 100 points (normal motor performance). Divided into 66 points for upper extremity and 34 points for the lower extremity. Sensory functioning (from 0 to 24 points) Balance (from 0 to 14) Joint range of motion (from 0 to 44) Joint pain (from 0 to 44 ) Scale items are scored on the basis of ability to complete the item using a 3-point ordinal scale where 0=cannot perform, 1=performs partially and 2=performs fully. The total possible scale score is 226.
Time Frame
At baseline-day 0 (T0), the middle of the treatment-day 15 (T1), at the end treatment-day 30 (T2), and at the follow up visit-day 90 (2 months both for the hospital-based and for the home based program) (T3)
Secondary Outcome Measure Information:
Title
Change in Frenchay Arm Test (FAT)
Description
The Frenchay Arm Test (FAT) is a measure of upper extremity proximal motor control and dexterity during ADL performance in patients with impairments resulting from neurological conditions. The FAT is an upper extremity specific measure of activity limitation.
Time Frame
At baseline-day 0 (T0), the middle of the treatment-day 15 (T1), at the end treatment-day 30 (T2), and at the follow up visit-day 90 (2 months both for the hospital-based and for the home based program) (T3)
Other Pre-specified Outcome Measures:
Title
Change in Box and Block Test (BBT)
Description
The Box and Block Test (BBT) measures unilateral gross manual dexterity. It is a quick, simple and inexpensive test. It can be used with a wide range of populations, including clients with stroke.
Time Frame
At baseline-day 0 (T0), the middle of the treatment-day 15 (T1), at the end treatment-day 30 (T2), and at the follow up visit-day 90 (2 months both for the hospital-based and for the home based program) (T3)
Title
Change in Modified Ashworth Scale (MSA)
Description
The Modified Ashworth scale (MAS) measures resistance during passive soft-tissue stretching and is used as a simple measure of spasticity.[1] Scoring (taken from Bohannon and Smith, 1987): 0: No increase in muscle tone Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the range of motion when the affected part(s) is moved in flexion or extension 1+: Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the Range Of Motion (ROM) More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved Considerable increase in muscle tone, passive movement difficult Affected part(s) rigid in flexion or extension
Time Frame
At baseline-day 0 (T0), the middle of the treatment-day 15 (T1), at the end treatment-day 30 (T2), and at the follow up visit-day 90 (2 months both for the hospital-based and for the home based program) (T3)
Title
Change in Modified Bartel Index (mBI)
Description
The Modified Bartel Index (mBI) is an ordinal scale used to measure performance in activities of daily living (ADL). Each performance item is rated on this scale with a given number of points assigned to each level or ranking. It uses ten variables describing ADL and mobility. A higher number is associated with a greater likelihood of being able to live at home with a degree of independence following discharge from hospital.
Time Frame
At baseline-day 0 (T0), the middle of the treatment-day 15 (T1), at the end treatment-day 30 (T2), and at the follow up visit-day 90 (2 months both for the hospital-based and for the home based program) (T3)
Title
Change in Chedoke-McMaster Stroke Assessment scale
Description
The Chedoke-McMaster Stroke Assessment measures physical impairment and disability in people with stroke and other neurological impairment. The measure consists of an Impairment Inventory and an Activity Inventory (Moreland, Gowland, Van Hullenaar, & Huijbregts, 1993). The first inventory aims to determine the presence and severity of common physical impairments, to classify or stratify patients when planning, selecting interventions and evaluating their effectiveness and to predict outcomes. The second inventory measures changes in physical function (Gowland, Stratford, Ward, Moreland, Torresin, Van Hullenar, Sanford, Barreca, Vanspall, & Plews, 1993). No helper needed 7 Complete Independence (Timely, Safely) 6 Modified Independence 5 Supervision A helper needed 4 Minimal Assist (Client = 75%) 3 Moderate Assist (Client = 50%) Complete Dependence 2 Maximal Assist (Client = 25%) 1 Total Assist (Client = 0%)
Time Frame
At baseline-day 0 (T0), the middle of the treatment-day 15 (T1), at the end treatment-day 30 (T2), and at the follow up visit-day 90 (2 months both for the hospital-based and for the home based program) (T3)
Title
Change in Mini-Mental state examination (MMSE)
Description
Il Mini-Mental State Examination (MMSE) (Folstein et al., 1975), is a neuropsychological test for the assessment of intellectual efficiency disorders and the presence of cognitive deterioration. The total score is between a minimum of 0 and a maximum of 30 points, where a score of 30 represents the best cognitive condition, and 0 the worst. The Mini-Mental state examination (MMSE) is often used as a screening tool in the investigation of subjects with dementia, and with neuropsychological syndromes of different nature.
Time Frame
At baseline-day 0 (T0), at the end treatment-day 30 (T2) and at the follow up visit-day 90 (2 months both for the hospital-based and for the home based program) (T3)
Title
Change in ElectroEncephaloGraphy (EEG)
Description
Electroencephalography (EEG) is an electrophysiological monitoring method to record electrical activity of the brain. It is noninvasive, with the electrodes placed over the scalp. Each conscious and unconscious mental function is the result of the electrical communication among the human brain neurons. It is not possible to record in a no-invasive way the electrical activity related to each neuron, however the EEG technique is able to measure the voltage fluctuations over the scalp caused by the concomitant electrical activity of a neurons population. Such voltage fluctuations could be characterized in terms of spectral content (EEG rhythms or bands) or of time-domain characteristics (Evoked Potentials and Event-Related Potentials). Alph (8-13 Htz), Beta (14-30 Htz) and Mu (8-13 Htz) bandwidth will be registered. The last band will be analysed specifically to investigate the motor areas and mirror neuron system's activity.
Time Frame
At baseline-day 0 (T0), at the end treatment-day 30 (T2) and at the follow up visit-day 90 (2 months both for the hospital-based and for the home based program) (T3)
Title
Change in surface ElectroMioGraphy (sEMG) - arm and shoulder muscles
Description
Surface electromyography (sEMG) is a non-invasive procedure involving the detection, recording and interpretation of the electric activity of groups of muscles at rest (i.e., static) and during activity (i.e., dynamic). The procedure is performed using a single or an array of electrodes placed on the skin surface over the muscles to be tested. Recording can also be made using a hand-held device, which is applied to the skin surface at different sites. Electrical activity is assessed by computer analysis of the frequency spectrum, amplitude, or root mean square of the electrical action potential.
Time Frame
At baseline-day 0 (T0), at the end treatment-day 30 (T2) and at the follow up visit-day 90 (2 months both for the hospital-based and for the home based program) (T3)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: chronic stroke (never experienced AOT); first-ever unilateral stroke due to ischemia provoking a clinically evident upper limb/hand deficit; diagnosis verified by brain imaging (MRI); cognitive function sufficient to understand the experimental instructions Chedoke-McMaster stroke Assessment Scale score greater than 1; informed written consent to participate in the study. Exclusion Criteria: bilateral impairment, severe sensory deficits in the paretic upper limb, cognitive impairment or behavioral dysfunction, refusal or inability to provide informed consent and other current severe medical problems.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Francesco Infarinato, Phd
Phone
+39065225
Ext
3788
Email
francesco.infarinato@sanraffaele.it
First Name & Middle Initial & Last Name or Official Title & Degree
Sanaz Pournajaf, PT
Phone
+39065225
Ext
2319
Email
sanaz.pournajaf@sanraffaele.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francesco Infarinato, Phd
Organizational Affiliation
IRCSS San Raffaele Pisana
Official's Role
Study Chair
Facility Information:
Facility Name
Casa di Cura del Policlinico di Milano
City
Milan
State/Province
MI
Country
Italy
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Irma Sterpi, PhD
Email
i.sterpi@ccppdezza.it
First Name & Middle Initial & Last Name & Degree
Irma Sterpi, PhD
Facility Name
IRCCS San Raffaele Pisana
City
Rome
State/Province
RM
ZIP/Postal Code
00166
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Astrid Van Rijn
Phone
+39-065225
Ext
3405
Email
astrid.vanrijn@sanraffaele.it
First Name & Middle Initial & Last Name & Degree
Sanaz Pournajaf, PT
Phone
+39-065225
Ext
2319
Email
sanaz.pournajaf@sanraffaele.it
First Name & Middle Initial & Last Name & Degree
Francesco Infarinato, Phd
First Name & Middle Initial & Last Name & Degree
Sanaz Pournajaf, PT

12. IPD Sharing Statement

Plan to Share IPD
No
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Neuroimaging Biomarkers Toward a Personalized Upper Limb Action Observation Treatment in Chronic Stroke Patients

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