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Radial Extracorporeal Shock Wave Therapy and Visual Feedback Balance Training on Lower Limb Post-Stroke Spasticity, Trunk Performance and Balance:

Effectiveness of Radial Extracorporeal Shock Wave Therapy and Visual Feedback Balance Training on Lower Limb Post-Stroke Spasticity, Trunk Performance and Balance: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05196633
Enrollment
23
Registered
2022-01-19
Start date
2021-01-01
Completion date
2021-08-31
Last updated
2024-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke, Ischemic, Stroke Hemorrhagic, Spasticity as Sequela of Stroke, Spastic Gait, Balance; Distorted

Keywords

stroke, spasticity, balance trainer, balance impairment, neurologic rehabilitation

Brief summary

This study assess the relationship between lower limb spasticity and trunk movements during static and dynamic balance in post-stroke patients who also underwent conventional physical therapy, visual feedback balance training and radial extracorporeal shock wave therapy intervention.

Detailed description

The stabilometric assessment through Prokin system complemented the clinical evaluation and provided a more objective, global insight into the combined therapeutic effect. The stabilometric computerized system is both an assessment tool and a training system for static, dynamic balance and trunk. To date, it was used in various clinical trials as a training tool for promoting stance and balance improvement in several neurorehabilitation programs. Additional outcomes focused on the effectiveness on pain intensity, clonus, passive range of motion, lower limb sensorimotor function, and functionality. The adverse events were also attentively monitored during the trial.

Interventions

rESWT (Endopuls 811; Enraf Nonius B.V. Va-reseweg 127, 3047 AT Rotterdam MedTech, Wessling, Germany) will be applied on the myotendinous junction of both the gastrocnemius and the soleus muscles in post-stroke spasticity patients. 2000 shots will be applied on the gastrocnemius and soleus myotendinous junction with a frequency of 10 Hz and energy density of 60 mJ (1 bar) within tolerable pain limits.

The control group will receive sound over the myotendinous junction of gastrocnemius and soleus with transducer-like contact.

Sponsors

Carol Davila University of Medicine and Pharmacy
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* a hemorrhagic or ischemic stroke in acute, subacute or chronic phase; * no history of previous stroke; * lower limb post-stroke spasticity and spasticity grade ≥1 on the Modified Ashworth Scale (MAS); * pain intensity measured on Visual Analogue Scale (VAS) ≥1; * ability to stand unassisted in upright position for 30 seconds; * no change in anti-spastic drug dose or treatment and no changes in analgesic medication, as it could affect the results on the Modified Ashworth Scale and the Visual Analogue Scale * adult patients (\>18 years old)

Exclusion criteria

* other neurological and orthopaedic disorders or lower limb deformities that could in-terfere with motor performance and balance; * myopathies; * severe cognitive impairment, severe aphasia or inability to understand instructions; * severe spasticity; * visual field conditions or hemineglect; * patients unable to undergo follow-up evaluation and excluded from the final analysis; * anticoagulant medication or any contraindication to receive radial extracorporeal shockwave therapy (rESWT), or any contraindication to physical therapy.

Design outcomes

Primary

MeasureTime frameDescription
Spasticity grade changeChange from baseline Modified Ashworth Scale at 14 daysThe Modified Ashworth Scale (MAS)

Secondary

MeasureTime frameDescription
Range of motion changeChange from baseline Passive Range of Motion at 14 dayspassive range of motion (PROM) parameter measured through a hand-held goniometer
Pain intensity changeChange from baseline Visual Analogue Scale at 14 daysVisual Analogue Scale (VAS) through a vertical 10-cm line (0 - starting pain-free to 10 - the worst imaginable pain). The higher the score means a worse outcome.
Stabilometric outcomes changeChange from baseline Prokin system parameters at 14 daysProkin system (PK 252, TecnoBody, Bergamo, Italy) parameters: trunk (degrees), stance (degrees), static (mm\^2) and dynamic balance (mm\^2)

Countries

Romania

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026