Radial Extracorporeal Shock Wave Therapy and Visual Feedback Balance Training on Lower Limb Post-… (NCT05196633) | Clinical Trial Compass
CompletedNot Applicable
Radial Extracorporeal Shock Wave Therapy and Visual Feedback Balance Training on Lower Limb Post-Stroke Spasticity, Trunk Performance and Balance:
Romania23 participantsStarted 2021-01-01
Plain-language 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.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
What they're measuring
1
Spasticity grade change
Timeframe: Change from baseline Modified Ashworth Scale at 14 days
Trial details
NCT IDNCT05196633
SponsorCarol Davila University of Medicine and Pharmacy