Effect of Extracorporeal Shock Wave Therapy on Spasticity and Mobility in Stroke Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Extracorporeal Shock Wave Therapy (ESWT), Sham Extracorporeal Shock Wave Therapy.
- Who it may be relevant to
- Registry conditions: Stroke, Post-Stroke Spasticity, Lower Limb Spasticity. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Efficacy of Extracorporeal Shock Wave Therapy on Spasticity, Mobility, Motor Function, and Health-Related Quality of Life in Stroke Survivors: A Prospective Randomized Sham-Controlled Trial
Overview
This study aims to evaluate the effectiveness of extracorporeal shock wave therapy (ESWT) in individuals with lower limb spasticity following stroke. Spasticity is a common complication after stroke and can negatively affect walking ability, mobility, and quality of life. Participants will be randomly assigned to one of two groups. Both groups will receive a standard physiotherapy and rehabilitation program. In addition, the intervention group will receive ESWT applied to the lower limb muscles, while the control group will receive a sham (placebo) ESWT application. The treatment program will be conducted three times per week for four weeks. Clinical assessments will be performed at baseline, after treatment, and during follow-up. The main outcomes of the study include muscle tone (spasticity), walking performance, motor function, and quality of life. The results of this study may help improve rehabilitation strategies and provide evidence for the use of ESWT in stroke patients.
Detailed description
Stroke is one of the leading causes of long-term disability worldwide and is frequently associated with motor impairments, including spasticity. Post-stroke spasticity is characterized by increased muscle tone, exaggerated tendon reflexes, and resistance to passive movement, which can significantly impair functional mobility, gait performance, and independence in daily activities. Lower limb spasticity, particularly involving the plantar flexor muscles, plays a critical role in limiting walking ability and increasing the risk of falls.
Conventional treatment approaches for spasticity include physiotherapy interventions, oral medications, and botulinum toxin injections. However, these methods may have limited effectiveness, potential side effects, or high costs. Therefore, there is a need for alternative, non-invasive, and effective treatment options.
Extracorporeal shock wave therapy (ESWT) has recently emerged as a promising non-invasive modality for the management of spasticity. ESWT is thought to reduce muscle tone by altering muscle viscoelastic properties, modulating neuromuscular transmission, and improving local blood circulation. Previous studies have suggested beneficial effects of ESWT on spasticity; however, evidence regarding its impact on functional outcomes such as gait performance and quality of life remains limited and inconsistent.
This study is designed as a prospective, randomized, single-blind, sham-controlled clinical trial conducted at a tertiary rehabilitation center. A total of 85 participants with chronic stroke (≥3 months) and lower extremity spasticity (Modified Ashworth Scale ≥1+) will be recruited. Participants will be randomly assigned to either the ESWT group or the control group using a block randomization method.
The intervention group will receive radial ESWT applied to the gastrocnemius and soleus muscles in addition to a standard physiotherapy program. The ESWT parameters will include an energy flux density of 0.10-0.20 mJ/mm², frequency of 5-8 Hz, and 2000-3000 pulses per muscle, administered three times per week for four weeks. The control group will receive sham ESWT with identical procedures but without therapeutic energy delivery. Both groups will undergo a standardized rehabilitation program consisting of stretching, strengthening, balance training, and gait training.
Outcome measures will be assessed at baseline, post-treatment (4 weeks), and follow-up (8 weeks). The primary outcome is spasticity measured by the Modified Ashworth Scale (MAS). Secondary outcomes include walking performance assessed by the 10-Meter Walk Test (10MWT) and Timed Up and Go (TUG) test, motor function assessed by the Fugl-Meyer Assessment for the lower extremity (FMA-LE), and health-related quality of life assessed by the Stroke-Specific Quality of Life (SS-QOL) scale.
The findings of this study are expected to provide high-quality evidence regarding the clinical effectiveness of ESWT in reducing spasticity and improving functional outcomes in stroke survivors. This may contribute to the development of more effective and evidence-based rehabilitation strategies.
Interventions
- Device Extracorporeal Shock Wave Therapy (ESWT)
Radial extracorporeal shock wave therapy will be applied with an energy flux density of 0.10-0.20 mJ/mm², frequency of 5-8 Hz, and 2000-3000 pulses per muscle. Treatment will be administered three times per week for four weeks. - Device Sham Extracorporeal Shock Wave Therapy
A sham ESWT procedure will be performed using the same device without energy transmission, mimicking the sound and sensation of treatment.
Primary outcome measures
- Change in Spasticity Assessed by Modified Ashworth Scale (MAS) [Time frame: Baseline, 4 weeks (post-treatment), and 8 weeks (follow-up)]
Secondary outcome measures (5)
- Change in Walking Speed Assessed by 10-Meter Walk Test (10MWT) [Time frame: Baseline, 4 weeks, 8 weeks]
- Change in Functional Mobility Assessed by Timed Up and Go Test (TUG) [Time frame: Baseline, 4 weeks, 8 weeks]
- Change in Motor Function Assessed by Fugl-Meyer Assessment - Lower Extremity (FMA-LE) [Time frame: Baseline, 4 weeks, 8 weeks]
- Change in Functional Exercise Capacity Assessed by 6-Minute Walk Test (6MWT) [Time frame: Baseline, 4 weeks, 8 weeks]
- Change in Health-Related Quality of Life Assessed by Stroke-Specific Quality of Life Scale (SS-QOL) [Time frame: Baseline, 4 weeks, 8 weeks]
Eligibility criteria
Inclusion criteria
- Adults aged 18-65 years
- Diagnosed with ischemic or hemorrhagic stroke at least 3 months prior to enrollment Presence of lower extremity spasticity with a Modified Ashworth Scale (MAS) score ≥1+
- Ability to walk independently with or without assistive devices
- Ability to understand and follow instructions for exercise interventions and assessments
- Provided written informed consent
Exclusion criteria
- Receipt of botulinum toxin injection in the affected lower limb within the last 3 months
- Severe cognitive impairment preventing participation in assessments
- Presence of fixed joint contractures limiting range of motion
- Orthopedic or musculoskeletal disorders affecting lower limb function (e.g., fracture, severe osteoarthritis)
- Uncontrolled cardiovascular, respiratory, or systemic disease contraindicating exercise
- Participation in another interventional clinical trial
- Any condition judged by the investigator to interfere with participation or safety
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07523243 · IMU-2026 · IMU-2026 -STROKE