About this trial
Midportion Achilles tendinopathy is a common cause of pain and functional limitation in both athletes and the general population. Progressive tendon loading programs are considered first-line treatment but do not lead to satisfactory outcomes in all patients. Extracorporeal shockwave therapy (ESWT) and platelet-rich plasma (PRP) injections are commonly used interventions for refractory symptoms, yet evidence supporting their combined use is limited particularly in treating Achilles tendon disorders.
This randomized controlled trial will evaluate the effectiveness of a standardized exercise program alone or in combination with PRP injection, ESWT, or both therapies in active adults with midportion Achilles tendinopathy. Participants will be randomized to one of four treatment groups and followed for six months. The primary outcome will assess changes in Achilles tendon symptoms and function using the Victorian Institute of Sport Assessment-Achilles (VISA-A) score. Secondary outcomes will include patient-reported outcomes, physical function testing, ultrasound tendon structure measures, and gait biomechanics.
Eligibility criteria
Qualifiers
Age 18-65 years
Diagnosis of unilateral midportion Achilles tendinopathy
Symptoms present for more than 3 months
VISA-A score <80 at baseline
Disqualifiers
Symptoms present for less than 3 months
Prior PRP injection or ESWT treatment to the Achilles tendon within 3 months
Other lower extremity musculoskeletal injury affecting function
Symptomatic arthritis affecting the ankle or foot
Trial design
Treatments tested in this trial
- Platelet Rich Plasma
- Extracorporeal Shockwave Therapy
- Sham PRP
- Sham ESWT
Treatment groups
Sponsors and collaborators
Spaulding Rehabilitation Hospital
Lead sponsor
Storz Medical AG
Collaborator
Foundation for Physical Medicine and Rehabilitation
Collaborator