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Music Therapy for Rehabilitation in Stroke Patients (SONICHAND)

Primary Purpose

Stroke, Hand Injuries

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
STANDARD REHAB
SONICHAND
Sponsored by
Istituti Clinici Scientifici Maugeri SpA
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Music therapy, Sonification technique, Rehabilitation

Eligibility Criteria

40 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 40-85 years old
  • ischemic lesion in one hemisphere (hemiplegia / hemiparesis right or left)
  • Mini Mental State Examination > 24 onset acute event not later than 180 days prior to study entry

Exclusion Criteria:

  • Dated lesions beyond 6 months from onset
  • Multiple or bilateral lesions
  • Mini Mental State Examination <24
  • Presence of neglect
  • Previous or concomitant disabling diseases for upper limb function (Eg: Parkinson's disease, multiple sclerosis, shoulder's periarthritis, Dupuytren's disease, etc.)
  • Previous rehabilitative treatments with music

Sites / Locations

  • ICS Maugeri, Nervi Institute
  • ICS Maugeri, Montescano Institute
  • ICS Maugeri, Pavia Institute
  • Fondazione Santa Lucia IRCCS

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

SONICHAND

STANDARD REHAB

Arm Description

The intervention is similar to the standard protocol (15 minutes of warm-up plus 20 minute of training) but involves the sonification of the exercises (4 weeks, daily)

The rehabilitative standard intervention (Occupational Therapy) consists of 15 minutes of warm-up exercises plus a 20 minutes training for 4 weeks (daily)

Outcomes

Primary Outcome Measures

Fugl-Meyer Motor Assessment Scale
Primary endpoint of the study is given by the measurement of proximal and distal upper limb motor skills assessed by the Fugl-Meyer Motor Assessment Scale. The primary endpoint will be assessed by comparing the variation between T0 and T2 of the scale scores above mentioned in the experimental and control groups.

Secondary Outcome Measures

Box and Block Test (BBT)
Assessment of unilateral gross manual dexterity
Modified Ashworth Scale
Measurement of spasticity
Visual Analogue Scale (VAS)
Evaluation of perceived fatigue
Numerical Pain Rating Scale (NPRS)
Assessment of pain intensity
McGill Quality of Life
Assessment of Quality of Life

Full Information

First Posted
August 4, 2017
Last Updated
April 26, 2021
Sponsor
Istituti Clinici Scientifici Maugeri SpA
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1. Study Identification

Unique Protocol Identification Number
NCT03306797
Brief Title
Music Therapy for Rehabilitation in Stroke Patients
Acronym
SONICHAND
Official Title
Hand Rehabilitation With Music Therapy Technique (Sonification) and Leap Motion Controller in Stroke Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
March 28, 2017 (Actual)
Primary Completion Date
May 15, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Istituti Clinici Scientifici Maugeri SpA

4. Oversight

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

5. Study Description

Brief Summary
The study uses a specific hand tracking sensor (Leap Motion Controller) to catch the movements of the arm combined with proper pre-defined musical patterns (sonification) in a neurologic music therapy perspective. The aim of the experiment is to verify the efficacy of sonification technique (compared to usual care) in the hand rehabilitation of patients with stroke.
Detailed Description
Introduction: Every year in Italy occur over than 200.000 new stroke cases. The virtual and augmented reality offers a valid support to the rehabilitation program by providing objectives parameters for the patient evaluation, accelerating the motor recovery process and enhancing the motor performance after the discharge. This study uses a specific hand tracking sensor (Leap Motion Controller) to catch the movements of the arm combined with proper pre-defined musical patterns (sonification) in a neurologic music therapy perspective. In addition to its use in relational contexts, in fact, music therapy is widely used in the field of rehabilitation, and in particular in the neuromotor rehabilitation, due to the impact of the sound, as well as on paralimbic and limbic areas, the areas of the brain involved in the movements (motor cortex, supplementary motor area, cerebellum, basal ganglia, etc.). Recent studies uses sonification for the rehabilitation of the upper limbs assuming a replacement of the proprioceptive aspects damaged by the disease thanks to the audio-motor feedback. This study, furthermore, exploits the specificities of the Leap Motion Controller and the peculiarities of the sound stimuli that accompany the arm movement without requiring cognitive tasks. Objectives: To verify through a randomized controlled trial and a suitable motor assessment the efficacy of the rehabilitation of the hand in patients with stroke using the "sonification" technique To verify whether the "sonification" technique reduces the fatigue and the pain perceived during rehabilitation Assess the impact of "sonification" technique on patients quality of life Materials and Methods: In this randomized controlled trial 66 patients with stroke will be recruited and allocated in 2 groups. The control group will be undergone to a 35 minutes standard daily rehabilitation treatment lasting 4 weeks. The experimental group will be undergone to an analogue treatment based on 15 minutes of standard rehabilitation and 20 minutes of exercises with sonification. Randomisation will be centralized for the four Units involved in the study. The intervention will be assessed in blind at the baseline (T0), at the mid-treatment period (T1 = 2 weeks), at the end of the treatment (T2 = 4 weeks), and at a follow-up point (T3 = 8 weeks). The following assessment tools will be used: Fugl-Meyer Motor Assessment Scale Box and Block Test Modified Ashworth Scale Visual Analogue Scale (VAS) Numerical Pain Rating Scale McGill Quality of Life At T0, T1, T2 and T3 some motion parameters will be recorded and monitored by the Leap Motion Controller to evaluate possible changes in the movements execution. Statistics: The Intention-To-Treat (ITT) population will be considered for the analysis. An unpaired Student's t test on the pre (T0)-post treatment (T2) differences will be used to assess the primary endpoint. Longitudinal trends over time will be assessed through repeated measures analysis of variance. Other analyses will be available in the statistical analysis plan.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Hand Injuries
Keywords
Music therapy, Sonification technique, Rehabilitation

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
SONICHAND
Arm Type
Experimental
Arm Description
The intervention is similar to the standard protocol (15 minutes of warm-up plus 20 minute of training) but involves the sonification of the exercises (4 weeks, daily)
Arm Title
STANDARD REHAB
Arm Type
Other
Arm Description
The rehabilitative standard intervention (Occupational Therapy) consists of 15 minutes of warm-up exercises plus a 20 minutes training for 4 weeks (daily)
Intervention Type
Other
Intervention Name(s)
STANDARD REHAB
Intervention Description
The rehabilitative standard intervention (Occupational Therapy) consists of 15 minutes of warm-up exercises plus a 20 minutes training with at least 6 exercises selected from: wrist ulnarization radialization prono-supination horizontal flexion-extension vertical flexion-extension hand grasping pinching extensors interosseous shoulder-elbow vertical flexion-extension push forward
Intervention Type
Device
Intervention Name(s)
SONICHAND
Intervention Description
The intervention is similar to the standard protocol (15 minutes of warm-up plus 20 minute of training) but involves the sonification of the exercises selected from the list. The Leap Motion Controller is managed with an ad-hoc developed application that is able to associate the movements with a 4 notes arpeggio or with a modulated texture. With the first mode the movement produces and modulates an harmonic progression built on the consecutive grades of the major scale played as ascending and descending arpeggio with also a volume crescendo and decrescendo. With the second mode, the movement modulates the volume and the low-pass cutoff frequency of a synthetic texture.
Primary Outcome Measure Information:
Title
Fugl-Meyer Motor Assessment Scale
Description
Primary endpoint of the study is given by the measurement of proximal and distal upper limb motor skills assessed by the Fugl-Meyer Motor Assessment Scale. The primary endpoint will be assessed by comparing the variation between T0 and T2 of the scale scores above mentioned in the experimental and control groups.
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Box and Block Test (BBT)
Description
Assessment of unilateral gross manual dexterity
Time Frame
up to 8 weeks
Title
Modified Ashworth Scale
Description
Measurement of spasticity
Time Frame
up to 8 weeks
Title
Visual Analogue Scale (VAS)
Description
Evaluation of perceived fatigue
Time Frame
up to 8 weeks
Title
Numerical Pain Rating Scale (NPRS)
Description
Assessment of pain intensity
Time Frame
up to 8 weeks
Title
McGill Quality of Life
Description
Assessment of Quality of Life
Time Frame
up to 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 40-85 years old ischemic lesion in one hemisphere (hemiplegia / hemiparesis right or left) Mini Mental State Examination > 24 onset acute event not later than 180 days prior to study entry Exclusion Criteria: Dated lesions beyond 6 months from onset Multiple or bilateral lesions Mini Mental State Examination <24 Presence of neglect Previous or concomitant disabling diseases for upper limb function (Eg: Parkinson's disease, multiple sclerosis, shoulder's periarthritis, Dupuytren's disease, etc.) Previous rehabilitative treatments with music
Facility Information:
Facility Name
ICS Maugeri, Nervi Institute
City
Genoa
State/Province
Genova
Country
Italy
Facility Name
ICS Maugeri, Montescano Institute
City
Montescano
State/Province
Pavia
Country
Italy
Facility Name
ICS Maugeri, Pavia Institute
City
Pavia
ZIP/Postal Code
27100
Country
Italy
Facility Name
Fondazione Santa Lucia IRCCS
City
Rome
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
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Music Therapy for Rehabilitation in Stroke Patients

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