Early Radial Shock Waves Treatment on Spasticity in Patients With Stroke in Sub-acute Phase
Primary Purpose
Spasticity, Muscle, Extracorporeal Shockwave Therapy, Rehabilitation
Status
Terminated
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Radial Extracorporeal Shock Wave Therapy
Conventional physiotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Spasticity, Muscle
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of hemiparesis after an ischemic or hemorrhagic stroke
- Onset of spasticity within 3 months from acute stroke
- First-stroke survivors with confirmed brain lesions by tomography or magnetic resonance imaging
- Adults (age between 18 and 80 years)
- Post-stroke upper limb spasticity ranging 1-4 according to the Modified Ashworth Scale
Exclusion Criteria:
- No treatment of the limb spasticity with botulinum toxin, phenol, alcohol, or surgery in the last 6 months
- Presence of an unstable medical condition
- Contraindications to shock waves treatment (pregnancy, cancer, coagulopathies, pacemakers, skin pathologies)
- Global aphasia
- All subjects who scored above 25 on the Mini-Mental State Examination
Sites / Locations
- Stefano Brunelli
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
rSWT group
Control group
Arm Description
Radial Extracorporeal Shock Wave Therapy on spastic muscles of upper limb
conventional physiotherapy
Outcomes
Primary Outcome Measures
Change from baseline Modified Ashworth Scale at 9 weeks and at 13 weeks
A 6-point scale grading the resistance of a relaxed limb to rapid passive stretch
Secondary Outcome Measures
Change from baseline FUGL-MEYER ASSESSMENT UPPER EXTREMITY (FMA-UE) at 9 weeks and at 13 weeks
It is designed to assess motor functioning, sensation, pain and joint functioning in patients with post-stroke hemiplegia.
Change from baseline Barthel Index at 9 weeks and at 13 weeks
it is a 10-item ordinal scale that cover mobility and self-care domains; scores range from 0 (total dependence in ADL) to 100 (complete independence)
visual analogue scale (VAS)
to rate their degree of perceived benefit from treatment
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04365478
Brief Title
Early Radial Shock Waves Treatment on Spasticity in Patients With Stroke in Sub-acute Phase
Official Title
Effects of an Early Radial Shock Waves Therapy on Spasticity of the Upper Limb and on Functional Outcome in Patients With Stroke in Subacute Phase
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Terminated
Why Stopped
The study was suspended due to difficulties in recalling participants to follow up due to restrictions related to the COVID-19 pandemic
Study Start Date
May 2, 2020 (Actual)
Primary Completion Date
September 20, 2021 (Actual)
Study Completion Date
September 27, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Stefano Brunelli
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
Hands and wrist spasticity are a common post stroke complication and often lead to restrictions in daily living activities. Spasticity causes changes in muscle composition such as accumulation of collagenous connective tissue and progressive loss of skeletal muscle fibres and these changes start almost immediately after a vascular event. Radial Shock Wave Therapy (rSWT) is a valid alternative rehabilitating tool in managing chronic spasticity but no study has so far investigated the effect in a recently onset hemiparesis. The aim of this study is to evaluate the efficacy of an early radial shock wave therapy in improving spasticity of the upper limb in patients with a recent onset stroke. The secondary outcome is to investigate the improvement of upper limb motor functionality, passive range of motion and joint pain and to determine if it can lead to a better performance in daily living activities. This study is a randomized controlled trial double arm single blind. The investigators plan to enrol 40 hemiplegic patients with sub-acute stroke and randomly assign them to an experimental or control group. The experimental group (EG) will perform one radial shock wave therapy session a week for 8 weeks administered during the daily morning 40 minutes of conventional rehabilitation treatment. The control group (CG) 40-minutes of conventional rehabilitation treatment for 5 days per week in the morning for 8 weeks. All patients performed in the afternoon a second daily session of 40 minutes of conventional rehabilitation therapy 5 days per week. The Modified Ashworth Scale (MAS), Fugl-Meyer Assessment Upper Extremity (FMA-UE) (with motricity, Passive Range of Motion (PROM) and pain sub-scores of upper extremity part of the scale), Modified Barthel Index and Visual Analogue Scale (VAS) for patient's benefit perceived, will be evaluated before and a week after the last intervention. MAS will be administered once a week, before rSWT treatment. The investigators plan to have a 1 month follow up during which every outcome measure will be administered. The investigators hypothesize that radial shock waves therapy, started early and associated with traditional physiotherapy, may be more effective in promoting the reduction of spasticity and pain of the upper limb, improve its functionality and therefore a reduction in disability, compared to conventional rehabilitation treatment. A reduction in the use of analgesic and muscle relaxants drugs is also conceivable
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spasticity, Muscle, Extracorporeal Shockwave Therapy, Rehabilitation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
36 (Actual)
8. Arms, Groups, and Interventions
Arm Title
rSWT group
Arm Type
Experimental
Arm Description
Radial Extracorporeal Shock Wave Therapy on spastic muscles of upper limb
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
conventional physiotherapy
Intervention Type
Procedure
Intervention Name(s)
Radial Extracorporeal Shock Wave Therapy
Intervention Description
rSWT group: One radial shock wave therapy session a week for 8 weeks (parameters: 1.5 bar, 10 Hz, 2000 shots for each muscle group treated) administered daily during the morning for 40 minutes of conventional rehabilitation treatment.
Intervention Type
Procedure
Intervention Name(s)
Conventional physiotherapy
Intervention Description
Control group: 40-minutes of conventional rehabilitation treatment 5 days per week in the morning (strength exercise, trunk control exercise, stretching exercise, occupational therapy, and neurodevelopmental facilitation techniques) for 8 weeks
Primary Outcome Measure Information:
Title
Change from baseline Modified Ashworth Scale at 9 weeks and at 13 weeks
Description
A 6-point scale grading the resistance of a relaxed limb to rapid passive stretch
Time Frame
baseline the first rSWT treatment, at 9 weeks (1 week after the last treatment) and at 13 weeks (follow up at 4 weeks after the last treatment)
Secondary Outcome Measure Information:
Title
Change from baseline FUGL-MEYER ASSESSMENT UPPER EXTREMITY (FMA-UE) at 9 weeks and at 13 weeks
Description
It is designed to assess motor functioning, sensation, pain and joint functioning in patients with post-stroke hemiplegia.
Time Frame
baseline the first rSWT treatment, at 9 weeks (1 week after the last treatment) and at 13 weeks (follow up at 4 weeks after the last treatment)
Title
Change from baseline Barthel Index at 9 weeks and at 13 weeks
Description
it is a 10-item ordinal scale that cover mobility and self-care domains; scores range from 0 (total dependence in ADL) to 100 (complete independence)
Time Frame
baseline the first rSWT treatment, at 9 weeks (1 week after the last treatment) and at 13 weeks (follow up at 4 weeks after the last treatment)
Title
visual analogue scale (VAS)
Description
to rate their degree of perceived benefit from treatment
Time Frame
at 9 weeks (at the end of the last rESWT treatment)
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:
Diagnosis of hemiparesis after an ischemic or hemorrhagic stroke
Onset of spasticity within 3 months from acute stroke
First-stroke survivors with confirmed brain lesions by tomography or magnetic resonance imaging
Adults (age between 18 and 80 years)
Post-stroke upper limb spasticity ranging 1-4 according to the Modified Ashworth Scale
Exclusion Criteria:
No treatment of the limb spasticity with botulinum toxin, phenol, alcohol, or surgery in the last 6 months
Presence of an unstable medical condition
Contraindications to shock waves treatment (pregnancy, cancer, coagulopathies, pacemakers, skin pathologies)
Global aphasia
All subjects who scored above 25 on the Mini-Mental State Examination
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Noemi Gentileschi, MD
Organizational Affiliation
Fondazione Santa Lucia Roma Italy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stefano Brunelli
City
Roma
ZIP/Postal Code
00179
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data that underlie the results reported in this article, after deidentification (text, tables, figures, and appendices)
IPD Sharing Time Frame
Beginning 3 months and ending 5 years following article publication.
IPD Sharing Access Criteria
Investigators whose proposed use of the data has been approved by an independent review committee ("learned intermediary") identified for this purpose; For individual participant data meta-analysis.Proposals should be directed to the personal author's mail address
Citations:
PubMed Identifier
14684785
Citation
Sommerfeld DK, Eek EU, Svensson AK, Holmqvist LW, von Arbin MH. Spasticity after stroke: its occurrence and association with motor impairments and activity limitations. Stroke. 2004 Jan;35(1):134-9. doi: 10.1161/01.STR.0000105386.05173.5E. Epub 2003 Dec 18.
Results Reference
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PubMed Identifier
25638688
Citation
Lee SS, Spear S, Rymer WZ. Quantifying changes in material properties of stroke-impaired muscle. Clin Biomech (Bristol, Avon). 2015 Mar;30(3):269-75. doi: 10.1016/j.clinbiomech.2015.01.004. Epub 2015 Jan 21.
Results Reference
background
PubMed Identifier
16109905
Citation
Manganotti P, Amelio E. Long-term effect of shock wave therapy on upper limb hypertonia in patients affected by stroke. Stroke. 2005 Sep;36(9):1967-71. doi: 10.1161/01.STR.0000177880.06663.5c. Epub 2005 Aug 18.
Results Reference
background
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Early Radial Shock Waves Treatment on Spasticity in Patients With Stroke in Sub-acute Phase
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