Eccentric Exercise Versus Eccentric Exercise and Astym for Insertional Achilles Tendinopathy

Indiana University Health Ball Memorial Hospital Rehabiliation Services

Status: Completed

Conditions: Insertional Achilles Tendinopathy

Treatments: Other: Eccentric Exercise; Other: Astym

Study type: Interventional

Funder types: Other

Identifiers

NCT01988155

13-928

Details and patient eligibility

About

The purpose of this research study is to determine if Astym® treatment is an effective treatment for patients with Achilles pain. The usual treatment for this condition is a specific exercise program that has been previously shown to be effective. The research team is trying to determine if combining Astym with the exercise program is more effective than exercise program only.

The main hypothesis for this study is that Astym plus eccentric exercise will be more effective than eccentric exercise alone at improving pain and function in patients with insertional Achilles tendinopathy.

Enrollment: 16 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• diagnosis of insertional AT as a primary complaint*

• symptom duration of at least 6 weeks

• VISA-A score of 78 or lower

  • he presence of insertional AT will be clinically determined by the primary investigator using the following criteria: pain at or within 2 cm of the posterior calcaneal insertion of the Achilles tendon along with localized tenderness and a subjective report of decreased activity levels secondary to Achilles pain.

Exclusion criteria

• prior treatment with eccentric exercise or Astym for Achilles tendinopathy
• currently taking anticoagulant medication
• usage of fluoroquinolone antibiotics in the previous six months
• previous Achilles surgery on the involved side
• bilateral symptoms
• pregnancy
• worker's compensation or liability cases
• peripheral neuropathy
• signs of lumbar radiculopathy
• inability to complete the required outcomes forms or comply with the recommended treatment regimen

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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16 participants in 2 patient groups

Eccentric Exericse

Active Comparator group

Treatment:

Other: Eccentric Exercise

Astym

Experimental group

Treatment:

Other: Astym