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Physiotherapy and Action-Observation Therapy: An Integrated Approach for Upper Limb Impairment in Subacute Stroke (PHOENICS)

Primary Purpose

Stroke

Status
Not yet recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Virtual Reality
Action Observation Therapy
Landscape video
Standard treatment
Sponsored by
Fondazione Don Carlo Gnocchi Onlus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Upper limb impairment, Virtual Reality, Action Observation Therapy

Eligibility Criteria

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

Inclusion Criteria:

  • Participant who suffered from an ictus 3 to 6 months before (subacute phase);
  • Baseline scoring of the Upper Extremity portion of the Fugl Meyer between 20 and 60.

Exclusion Criteria:

  • Other neurological pathologies (including previous strokes);
  • Visual field impairments;
  • Neuropsychological deficits that prevents the understanding of the instructions or the execution of the treatment (e.g. aphasia, apraxia, neglect);
  • Baseline scoring of the Mini Mental State Examination (MMSE) lower that 24 (MMSE < 24);
  • Orthopaedic or musculoskeletal limitations that do not allow the execution of the treatment;
  • Clinical instability;
  • Inability to understand the instructions needed to perform the test and the planned evaluations;
  • People with electronic medical devices such as pacemakers;
  • Medical history of epilepsy.

Sites / Locations

  • Fondazione Don Carlo Gnocchi Onlus - Centro Ettore Spalenza

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Virtual Reality + Action Observation Therapy

Virtual Reality + Landscape video

Arm Description

Participants will see a video demonstrating the exercise they will be later asked to perform. The same procedure is performed for each of the four different exercises.

Participants will see a video demonstrating a natural landscape and later they will perform an exercise. The same procedure is performed for each of the four different exercises.

Outcomes

Primary Outcome Measures

Change of Upper limb function
Upper extremity portion of the Fugl Meyer (UE-FM). This scale measures the function of the upper limb in a range of 0 to 66 points. Higher values represent a better outcome.
Change of hand dexterity
Box and Block test. This test examines hand dexterity measuring the number of wooden blocks the participant is able to move from one box to another with the paretic hand in 60 seconds. Higher values represent a better outcome.

Secondary Outcome Measures

Change of autonomy
Barthel Index. This scale measures the ability of the subject to perform activities of daily living. Range 0-100. Higher values represent a better outcome.
Change of quality of Life
EuroQol-5D questionnaire. This questionnaire measures the quality of life. Range 5-15. Lower values represent a better outcome.
Change of level completed
Most difficult level the participant is able to complete, from 1 to 6. Higher values represent a better performance.
Change of number of correct tasks
Number of tasks the participants performs correctly. Higher values represent a better performance.
Change of reaction time
Seconds from the appearance of the target to the start of the movement. Lower values represent a better outcome.
Change of interaction time
Seconds from the appearance of the target to its reaching. Lower values represent a better outcome.
Change of mean time of exercise execution
Seconds required for single exercise execution. Lower values represent a better outcome.
Level of Satisfaction
Likert 1-5. This scale measures the level of satisfaction of the subject regarding the treatment. Higher values represent a better outcome.
Change of Hand Max Reaching Velocity
Maximal velocity (meters/seconds) of the hand movement during reaching of the target. Higher values represent a better outcome.
Change of % Cycle Hand Max Velocity
Dividing the interaction time between the hand and the object into 100 parts, it represents the moment in which the hand reaches the maximal velocity.
Change of Mean SPARC
Spectral parameter related to the smoothness of the movement. Negative values lower than -1 stand for lower smoothness.
Change of Mean Reach Path Ratio
Parameter calculated as total distance traveled by the wrist of the subject divided by the length of a straight-line path from the reach's starting point (hand resting on the table) to ending point (target). Values equal or close to +1 represent a straight trajectory, while higher values stand for a more curved one.
Change of Tip Max Distance
Maximal distance between the thumb and index fingertips.
Change of Tip Max Velocity
Maximal velocity of opening and closing between the thumb and index fingertips.

Full Information

First Posted
October 2, 2019
Last Updated
September 7, 2021
Sponsor
Fondazione Don Carlo Gnocchi Onlus
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1. Study Identification

Unique Protocol Identification Number
NCT04560764
Brief Title
Physiotherapy and Action-Observation Therapy: An Integrated Approach for Upper Limb Impairment in Subacute Stroke
Acronym
PHOENICS
Official Title
Virtual Reality and Action-Observation Therapy: An Integrated Approach Supported by Novel Technologies for Upper Limb Impairment in Subacute Stroke
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 1, 2023 (Anticipated)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fondazione Don Carlo Gnocchi Onlus

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Motor impairment is one of the most common result of a stroke, which causes disability and difficulties in activities of daily living. This motor impairment can concern the upper limb or the lower limb, or both. Several studies investigates the efficacy of different treatment approaches on upper limb and hand function. None of them combined exercise in a virtual context with Action Observation Therapy, consisting in watching an action before doing it. This study evaluates the addition of Action Observation Therapy (AOT) to Virtual Reality (VR) in the rehabilitation of upper limb impairment in subacute stroke patients. Half of participants will see a video demonstrating the exercise to be performed before its actual execution, while the other half will see a video of a natural landscape followed by the same exercises the other group performs. All the patients will receive additional usual treatment.
Detailed Description
In this study, the intervention will be conducted using a system composed by multiple devices, which are: HTC Vive (HTC, headset e Steam station): three-dimensional viewer used for the implementation of the immersive virtual environment, allows both the visualization of the videos and of the exercises to be performed; Leap Motion Controller (infrared camera): contactless device for tracking the movement of the patient's fingers and hand; Zed Mini (RGB binocular camera and depth camera): Stereo Labs' Zed Mini stereoscopic camera is mounted on the HTC Vive viewer to allow virtual elements to be overlapped within the environment; Cometa Wavetrack (transmitter/receiver and Inertial Measurement Units): system for upper limb movement tracking through the use of four wireless inertial sensors applied to the chest, to the arm and to the forearm of the participant through elastic bands and to the hand of the participant through skin-compatible double-sided adhesive patches. All the devices have been tested to ensure safety of the participants and are provided with the appropriate documentation of declaration of conformity according to the European reference regulations. A careful risk analysis was carried out to ensure the safety of the participants. All the devices will be working simultaneously during each session of treatment. For the experimental group, the instrumentation will be used to see the video of the exercises that the participants will be later asked to perform and to actually perform them; in the control group, it will be used to see a video of a natural landscape with a 180° perspective and to perform the same exercises than the experimental group. The devices will be used both for the execution of the exercises both to collect information listed in the outcomes section as secondary outcomes: in particular, these information will be provided by the Leap Motion and by the Cometa Wavetrack devices.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Upper limb impairment, Virtual Reality, Action Observation Therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
22 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Virtual Reality + Action Observation Therapy
Arm Type
Experimental
Arm Description
Participants will see a video demonstrating the exercise they will be later asked to perform. The same procedure is performed for each of the four different exercises.
Arm Title
Virtual Reality + Landscape video
Arm Type
Sham Comparator
Arm Description
Participants will see a video demonstrating a natural landscape and later they will perform an exercise. The same procedure is performed for each of the four different exercises.
Intervention Type
Device
Intervention Name(s)
Virtual Reality
Intervention Description
Participants in both groups will attend 10 sessions of approximately 30 minutes each three times a week. Each session contemplates the execution of a single repetition of two minutes of each of the four exercises. There are four exercises: Reaching: the participant is requested to reach a target in front of him with the paretic hand; the target will appear in a different place every time; Reaching and grasping: the participant is requested to grab a wooden cube with the paretic hand and place it into a bowl positioned in front of him; the cube will appear in a different place every time; Goalkeeper: the participant is requested to block a ball coming towards him with the paretic hand; the ball will appear in a different place every time; Occupational task: the participant is requested to grab four cans, one at time, with the paretic hand and place them on four targets placed on a hemispherical arch. Each exercise provides six levels of increasing difficulty.
Intervention Type
Device
Intervention Name(s)
Action Observation Therapy
Intervention Description
Before the execution of the exercises described in the intervention "Virtual Reality", the participants in the experimental group will see a video demonstrating the same exercise (according to the level of difficulty selected) he will be later asked to perform for two minutes.
Intervention Type
Device
Intervention Name(s)
Landscape video
Intervention Description
Before the execution of the exercises described in the intervention "Virtual Reality", the participants in the sham comparator group will see a video of a natural landscape for two minutes.
Intervention Type
Other
Intervention Name(s)
Standard treatment
Intervention Description
Participants in both groups will receive the standard treatment, one hour a day for three days a week.
Primary Outcome Measure Information:
Title
Change of Upper limb function
Description
Upper extremity portion of the Fugl Meyer (UE-FM). This scale measures the function of the upper limb in a range of 0 to 66 points. Higher values represent a better outcome.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of hand dexterity
Description
Box and Block test. This test examines hand dexterity measuring the number of wooden blocks the participant is able to move from one box to another with the paretic hand in 60 seconds. Higher values represent a better outcome.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Secondary Outcome Measure Information:
Title
Change of autonomy
Description
Barthel Index. This scale measures the ability of the subject to perform activities of daily living. Range 0-100. Higher values represent a better outcome.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of quality of Life
Description
EuroQol-5D questionnaire. This questionnaire measures the quality of life. Range 5-15. Lower values represent a better outcome.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of level completed
Description
Most difficult level the participant is able to complete, from 1 to 6. Higher values represent a better performance.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of number of correct tasks
Description
Number of tasks the participants performs correctly. Higher values represent a better performance.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of reaction time
Description
Seconds from the appearance of the target to the start of the movement. Lower values represent a better outcome.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of interaction time
Description
Seconds from the appearance of the target to its reaching. Lower values represent a better outcome.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of mean time of exercise execution
Description
Seconds required for single exercise execution. Lower values represent a better outcome.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Level of Satisfaction
Description
Likert 1-5. This scale measures the level of satisfaction of the subject regarding the treatment. Higher values represent a better outcome.
Time Frame
At the end of the treatment (4 weeks).
Title
Change of Hand Max Reaching Velocity
Description
Maximal velocity (meters/seconds) of the hand movement during reaching of the target. Higher values represent a better outcome.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of % Cycle Hand Max Velocity
Description
Dividing the interaction time between the hand and the object into 100 parts, it represents the moment in which the hand reaches the maximal velocity.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of Mean SPARC
Description
Spectral parameter related to the smoothness of the movement. Negative values lower than -1 stand for lower smoothness.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of Mean Reach Path Ratio
Description
Parameter calculated as total distance traveled by the wrist of the subject divided by the length of a straight-line path from the reach's starting point (hand resting on the table) to ending point (target). Values equal or close to +1 represent a straight trajectory, while higher values stand for a more curved one.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of Tip Max Distance
Description
Maximal distance between the thumb and index fingertips.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).
Title
Change of Tip Max Velocity
Description
Maximal velocity of opening and closing between the thumb and index fingertips.
Time Frame
Baseline (T0) and at the end of the treatment (T1, after 4 weeks).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participant who suffered from an ictus 3 to 6 months before (subacute phase); Baseline scoring of the Upper Extremity portion of the Fugl Meyer between 20 and 60. Exclusion Criteria: Other neurological pathologies (including previous strokes); Visual field impairments; Neuropsychological deficits that prevents the understanding of the instructions or the execution of the treatment (e.g. aphasia, apraxia, neglect); Baseline scoring of the Mini Mental State Examination (MMSE) lower that 24 (MMSE < 24); Orthopaedic or musculoskeletal limitations that do not allow the execution of the treatment; Clinical instability; Inability to understand the instructions needed to perform the test and the planned evaluations; People with electronic medical devices such as pacemakers; Medical history of epilepsy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Riccardo Buraschi, DPT
Phone
0039 3496657892
Email
rburaschi@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Riccardo Buraschi, DPT
Organizational Affiliation
IRCCS Fondazione Don Carlo Gnocchi
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fondazione Don Carlo Gnocchi Onlus - Centro Ettore Spalenza
City
Rovato
State/Province
Brescia
ZIP/Postal Code
25038
Country
Italy
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Riccardo Buraschi, DPT
Email
rburaschi@gmail.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
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Citation
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Laver KE, Lange B, George S, Deutsch JE, Saposnik G, Crotty M. Virtual reality for stroke rehabilitation. Cochrane Database Syst Rev. 2017 Nov 20;11(11):CD008349. doi: 10.1002/14651858.CD008349.pub4.
Results Reference
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PubMed Identifier
30380586
Citation
Borges LR, Fernandes AB, Melo LP, Guerra RO, Campos TF. Action observation for upper limb rehabilitation after stroke. Cochrane Database Syst Rev. 2018 Oct 31;10(10):CD011887. doi: 10.1002/14651858.CD011887.pub2.
Results Reference
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PubMed Identifier
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Physiotherapy and Action-Observation Therapy: An Integrated Approach for Upper Limb Impairment in Subacute Stroke

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