Music Therapy for Rehabilitation in Stroke Patients
- Conditions
- StrokeHand Injuries
- Interventions
- Device: SONICHANDOther: STANDARD REHAB
- Registration Number
- NCT03306797
- Lead Sponsor
- Istituti Clinici Scientifici Maugeri SpA
- 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 65
- 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
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description SONICHAND SONICHAND 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) STANDARD REHAB STANDARD REHAB The rehabilitative standard intervention (Occupational Therapy) consists of 15 minutes of warm-up exercises plus a 20 minutes training for 4 weeks (daily)
- Primary Outcome Measures
Name Time Method Fugl-Meyer Motor Assessment Scale 4 weeks 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
Name Time Method Numerical Pain Rating Scale (NPRS) up to 8 weeks Assessment of pain intensity
Box and Block Test (BBT) up to 8 weeks Assessment of unilateral gross manual dexterity
Visual Analogue Scale (VAS) up to 8 weeks Evaluation of perceived fatigue
Modified Ashworth Scale up to 8 weeks Measurement of spasticity
McGill Quality of Life up to 8 weeks Assessment of Quality of Life
Trial Locations
- Locations (4)
ICS Maugeri, Pavia Institute
🇮🇹Pavia, Italy
ICS Maugeri, Nervi Institute
🇮🇹Genoa, Genova, Italy
Fondazione Santa Lucia IRCCS
🇮🇹Rome, Italy
ICS Maugeri, Montescano Institute
🇮🇹Montescano, Pavia, Italy