Self-Reported Foot Strike Patterns and Sonographic Evidence of Achilles Tendinopathy in Asymptomatic Marathon Runners

Overview

About this study

The purpose of this study is to determine maximal sonographic cross-sectional area of Achilles tendons as well as other signs of Achilles tendinopathy (hypoechogenicity, hyperemia) in asymptomatic marathon runners participating in the Donna Marathon and determine if a relationship exists between self-identified foot-strike patterns, training regimen, and the cross-sectional area of the Achilles tendons.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Will be participating in the Donna marathon with goal of completing all 26.2 mi
  • Age 18+
  • Men and women

Exclusion Criteria:

  • Non-runners
  • Runner who is running a relay and/or not entire marathon distance
  • Age < 18
  • Prior surgery on Achilles tendon
  • Prior injection, dry needling, PRP, or Tenex of Achilles tendon
  • Pain in the Achilles tendon

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Jacksonville, Fla.

Mayo Clinic principal investigator

Sara Filmalter, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Additional contact information

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Phone: 800-664-4542 (toll-free)

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