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Feasibility of ESWT Treatment in Post-stroke Patients With Triceps Sural Spasticity (Waves2021)

Primary Purpose

Stroke

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
ESWT + Stretching
ESWT and SHAM + Stretching
Sponsored by
Azienda Unità Sanitaria Locale Reggio Emilia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Stroke, Triceps Sural Spasticity, Extracorporeal Shockwave Therapy

Eligibility Criteria

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

Inclusion Criteria:

  • Adult patients of legal age
  • Time elapsed since the stroke between 6 and 60 months
  • Autonomous or supervised walking with or without aids
  • Spasticity of the sural triceps> 1 on the MAS scale

Exclusion Criteria:

  • Joint stiffness of the lower limbs due to other pathologies (ex orthopedic or rheumatological);
  • Conditions that interfere with evaluation or collaboration in rehabilitation treatment (major psychiatric illnesses, clearly detectable cognitive deficits, severe pre-existing disabilities, sensory disturbances, etc.)
  • Focal antispasmodic toxin treatments in the previous 3 months or phenolic blocks in the previous 9 months in the treatment region
  • Treatments with central antispasmodic drugs with dosage modifications in the last week of starting treatment
  • Individual neurorehabilitation treatments in progress

Sites / Locations

  • Operational Unit of Physical Medicine and Rehabilitation AUSL - IRCCS Reggio EmiliaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Group I

Group II

Arm Description

Outcomes

Primary Outcome Measures

Feasibility of two kind treatments proposed
The intervention is feasible if at least 80% of the enrolled patients complete the entire treatment foreseen in the allocation group

Secondary Outcome Measures

Change in Walking Resistance
6 minute walking test
Change in Level of mobility and balance
Timed Up & Go Test
Change in spasticity
Modified Ashworth Scale (MAS). Score from 0 to 4, higher scores mean a worse outcome
Change in Passive ROM of the ankle in dorsiflexion
Passive ankle Range of Motion (p-ROM)
Change in Leg Pain
Numeric Pain Rating Scale (NPRS) Score from 0 to 10, higher scores mean a worse outcome
Change in Ability to carry out activities of daily living
Lower Extremity Functional Scale (LEFS). Score from 0 to 80, higher scores mean a better outcome.
Change in triceps clones
Presence of ankle clonus

Full Information

First Posted
February 5, 2022
Last Updated
February 15, 2022
Sponsor
Azienda Unità Sanitaria Locale Reggio Emilia
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1. Study Identification

Unique Protocol Identification Number
NCT05255549
Brief Title
Feasibility of ESWT Treatment in Post-stroke Patients With Triceps Sural Spasticity
Acronym
Waves2021
Official Title
ESWT Treatment in Post-stroke Patients With Triceps Sural: a Feasibility RCT
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Recruiting
Study Start Date
July 22, 2021 (Actual)
Primary Completion Date
July 22, 2022 (Anticipated)
Study Completion Date
July 22, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Azienda Unità Sanitaria Locale Reggio Emilia

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
The main objective is to evaluate the feasibility of two different rehabilitation protocols that differed from the number of treatment sessions (1 session of ESWT versus 3 weekly sessions of ESWT), in patients with triceps surae spasticity after stroke. In both arms the other ESWT parameters (types of ESWT, intensity, frequency, location) and stretching sessions are the same. Secondary objectives: to compare functional performances in these two groups of patients receiving the different rehabilitation protocol with ESWT, using the following parameters: - Six Minutes walking test (6MWT) ; - Time Up & Go (TUG); - Modified Ashworth scale (MAS); - Lower Extremity Functional Scale (LEFS); - passive ankle range of motion (p-ROM), pain (NRS); and presence of ankle clonus. These parameters are assessed during baseline (T0), after 4 weeks (T1) and after 12 weeks (T2).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Stroke, Triceps Sural Spasticity, Extracorporeal Shockwave Therapy

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Group I
Arm Type
Experimental
Arm Title
Group II
Arm Type
Sham Comparator
Intervention Type
Procedure
Intervention Name(s)
ESWT + Stretching
Intervention Description
3 weeks intervention: 3 sessions of ESWT, once a week 6 sessions of passive stretching, twice a week
Intervention Type
Procedure
Intervention Name(s)
ESWT and SHAM + Stretching
Intervention Description
3 weeks intervention: 1 sessions of ESWT + 2 sessions of Sham, once a week 6 sessions of passive stretching, twice a week
Primary Outcome Measure Information:
Title
Feasibility of two kind treatments proposed
Description
The intervention is feasible if at least 80% of the enrolled patients complete the entire treatment foreseen in the allocation group
Time Frame
T1 after 4 weeks from T0 (Enrollment)
Secondary Outcome Measure Information:
Title
Change in Walking Resistance
Description
6 minute walking test
Time Frame
T0 Enrollment, T1 after 4 weeks from T0, T2 after 12 weeks from T0
Title
Change in Level of mobility and balance
Description
Timed Up & Go Test
Time Frame
T0 Enrollment, T1 after 4 weeks from T0, T2 after 12 weeks from T0
Title
Change in spasticity
Description
Modified Ashworth Scale (MAS). Score from 0 to 4, higher scores mean a worse outcome
Time Frame
T0 Enrollment, T1 after 4 weeks from T0, T2 after 12 weeks from T0
Title
Change in Passive ROM of the ankle in dorsiflexion
Description
Passive ankle Range of Motion (p-ROM)
Time Frame
T0 Enrollment, T1 after 4 weeks from T0, T2 after 12 weeks from T0
Title
Change in Leg Pain
Description
Numeric Pain Rating Scale (NPRS) Score from 0 to 10, higher scores mean a worse outcome
Time Frame
T0 Enrollment, T1 after 4 weeks from T0, T2 after 12 weeks from T0
Title
Change in Ability to carry out activities of daily living
Description
Lower Extremity Functional Scale (LEFS). Score from 0 to 80, higher scores mean a better outcome.
Time Frame
T0 Enrollment, T1 after 4 weeks from T0, T2 after 12 weeks from T0
Title
Change in triceps clones
Description
Presence of ankle clonus
Time Frame
T0 Enrollment, T1 after 4 weeks from T0, T2 after 12 weeks from T0

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients of legal age Time elapsed since the stroke between 6 and 60 months Autonomous or supervised walking with or without aids Spasticity of the sural triceps> 1 on the MAS scale Exclusion Criteria: Joint stiffness of the lower limbs due to other pathologies (ex orthopedic or rheumatological); Conditions that interfere with evaluation or collaboration in rehabilitation treatment (major psychiatric illnesses, clearly detectable cognitive deficits, severe pre-existing disabilities, sensory disturbances, etc.) Focal antispasmodic toxin treatments in the previous 3 months or phenolic blocks in the previous 9 months in the treatment region Treatments with central antispasmodic drugs with dosage modifications in the last week of starting treatment Individual neurorehabilitation treatments in progress
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stefania Testoni, Dr
Phone
+39 0522296163
Email
stefania.testoni@ausl.re.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stefania Testoni, Dr
Organizational Affiliation
Azienda AUSLRE
Official's Role
Principal Investigator
Facility Information:
Facility Name
Operational Unit of Physical Medicine and Rehabilitation AUSL - IRCCS Reggio Emilia
City
Reggio Emilia
State/Province
Emilia Romagna
ZIP/Postal Code
42123
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stefania Testoni, Dr
Phone
+39 0522296163

12. IPD Sharing Statement

Learn more about this trial

Feasibility of ESWT Treatment in Post-stroke Patients With Triceps Sural Spasticity

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