About this trial
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 criteria
Qualifiers
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
Disqualifiers
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
Trial design
Treatments tested in this trial
- Neuromuscular Electrical Stimulation (NMES)