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Clinical Trials in Brazil / NCT07453485
Recruiting Not applicable

Immediate Effects of Neuromuscular Electrical Stimulation on Pain and Function in Achilles Tendon Disorders

NCT07453485 · tracked via the Priya Life Science Brazil tracker
Phase
Not applicable
Started
2026-01-06
Last updated
2026-03-06

Condition(s) studied

Achilles Tendinopathy (AT)Achilles Tendon Rupture

Investigational drug(s) / intervention(s)

Neuromuscular Electrical Stimulation (NMES)

Neuromuscular Electrical Stimulation (NMES): Neuromuscular electrical stimulation-induced contractions will be delivered using an electrical stimulator connected to a pair of 5×5 cm self-adhesive surface electrodes. Stimulation will be applied in a superimposed manner during voluntary movement, at a frequency of 75 Hz and a phase duration of 400 µs.

Study summary

The Achilles tendon exhibits high tensile strength and can withstand extremely high loads. However, it is susceptible to injuries such as tendinopathies and ruptures, which are associated with structural alterations and loss of function. Strategies have been investigated to enhance clinical rehabilitation. Nevertheless, the effects of neuromuscular electrical stimulation on pain and functional improvement, as well as the optimal dosing parameters for the rehabilitation of Achilles tendon injuries, remain inconclusive. The aim of this study is to compare the immediate effects of two electrical stimulation protocols on pain, functional performance, peripheral oxygen extraction, and maximal tendon displacement during a single leg heel rise functional task in patients with Achilles tendinopathy and/or a history of Achilles tendon rupture. In addition, this study aims to characterize Achilles tendon structural properties and ankle plantarflexor muscle strength in this population.

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: * Primary complaint of pain localized in the midportion (2-6 cm proximal to the calcaneus) or insertion of the Achilles tendon, and/or a history of Achilles tendon rupture occurring at least 3 months prior to assessment. * Pain on palpation of the Achilles tendon. * Pain during load-bearing activities Exclusion Criteria: * Exclusive diagnosis of bursitis confirmed by ultrasonographic assessment * Any other lower limb injury * History of lower limb surgery within the past year * Previous Achilles tendon tenoplasty performed less than 3 months prior to assessment

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Brasilia Brasília Federal District Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07453485 on ClinicalTrials.gov ↗ ← All trials in Brazil