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N/A Completed N=46 Randomized Treatment

Pilot Investigation to Evaluate Effectiveness of Shockwave Therapy, Photobiomodulation and Physical Therapy in the Management of Non-insertional Achilles Tendinopathy

Source: ClinicalTrials.gov NCT04725513 ↗
Enrolled (actual)
46
Serious AEs
0.0%
Results posted
Jan 2026
Primary outcomePrimary: Calf Raises Performed to Fatigue and Inability to Continue — 3; 8; 5 Calf raises

Summary

This is a randomized control trial with an elective cross over after three months to evaluate three different treatments in the management of non-insertional Achilles Tendinopathy. The treatment methods include physical therapy, shockwave therapy and photobiomodulation.

Outcome Measures

OutcomeResultp-value
PRIMARY
Calf Raises Performed to Fatigue and Inability to Continue
3; 8; 5
PRIMARY
Ultrasound Measurements in Change of Cross Sectional Area
-0.03; -0.05; -0.03
PRIMARY
Victorian Institute of Sports Assessment (VISA-A) Questionnaire
18; 33; 25

Eligibility Criteria

Inclusion Criteria

  • A diagnosis of mid-portion Achilles tendinopathy (including both unilateral and bilateral)
  • Running is the pre-injury primary form of physical activity and pre-injury would complete on average 10 miles per week or more of running
  • VISA-A <80 at baseline to be eligible

Exclusion Criteria

  • Less than 3 months of symptoms
  • Primary insertional Achilles tendinopathy
  • Diagnosis of rheumatological disease/connective tissue condition, symptomatic arthritis of foot and ankle, a primary running related injury outside Achilles tendinopathy, other contraindications to PBMT or SWT
  • Have received SWT within the past 3 months to their Achilles
  • Prior injection within 3 months
  • Currently enrolled in PT for more than 4 weeks for their condition
  • Women who are pregnant.
  • known history of Achilles tendon tear
  • currently taking oral steroid or fluoroquinolone class of antibiotics
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04725513). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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