Astym® Compared Eccentric Exercise for Chronic Mid-substance Achilles Tendinopathy
TerminatedNot applicableNCT01902433
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The purpose of this study is to compare the changes in pain and self-perceived function between two different treatments for Achilles tendinopathy: the Astym® protocol (a form of soft tissue mobilization using instruments) and a specific exercise protocol that involves strengthening the calf and Achilles tendon. Astym® (A-stim) is not an acronym, but rather stands for "A Stimulation" of the body's healing response, describing the physiologic process which occurs with Astym treatment. Astym is the trademark name of a non-invasive treatment where instruments are applied topically to locate unhealthy soft tissue, and to transfer mild to moderate pressure to the underlying soft tissue structures. The aim of Astym treatment is to eliminate scar tissue and stimulate tissue regeneration. Both the principal investigator and co-investigator have been trained and certified in administering the Astym treatment. The specific exercise protocol will involve exercises that strengthen the Achilles and calf through eccentric exercise. Eccentric exercise is a form of exercise where the benefit comes from applying a controlled lengthening stress to the muscle and tendon.
Study details
- Official title
- Astym® Treatment Compared With Eccentric Exercise in the Management of Chronic Mid-substance Achilles Tendinopathy: A Multisite a Randomized Controlled Trial
- Conditions
- Achilles Tendon Pain
- Interventions
- Procedure: Astym
- Sponsor
- Emily Slaven, PT, PhD
- Collaborators
- Performance Dynamics
- Organization
- University of Indianapolis
- Start date
- 2013-08
- Primary completion
- 2017-01
- Sex
- All
- Age range
- from 20 Years to 60 Years
- Results posted
- No results posted in this snapshot
- Countries
- United States
- Total sites listed
- 2
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria * Pain for 3 months or longer in the mid portion of only one Achilles tendon. * Must read, speak and understand English Exclusion Criteria * Previous surgery to the Achilles tendon that is currently painful * An injection into the Achilles tendon in the previous 4 weeks * Have symptoms in both Achilles tendons concurrently * Have taken fluoroquinolone antibiotics in the past 6 months
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01902433