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Clinical Trials/ISRCTN58161116
ISRCTN58161116
Completed
未知

The effect of combined Action Observation Therapy and eccentric exercises in the treatment of mid-portion Achilles Tendinopathy (AOTAT): a feasibility pilot randomised controlled trial.

niversity College Dublin0 sites30 target enrollmentDecember 23, 2020

Overview

Phase
未知
Intervention
Not specified
Conditions
Mid-portion Achilles Tendinopathy
Sponsor
niversity College Dublin
Enrollment
30
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

2022 Protocol article in https://pubmed.ncbi.nlm.nih.gov/35130966/ (added 09/02/2022) 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/36447250/ outcome results (added 14/12/2022)

Registry
who.int
Start Date
December 23, 2020
End Date
June 1, 2022
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity College Dublin

Eligibility Criteria

Inclusion Criteria

  • 1\. Unilateral pain in the mid\-portion (2\-7 cm proximal to insertion) of the achilles tendon
  • 2\. Pain lasting \=3 months
  • 3\. Experiencing morning pain or stiffness
  • 4\. Have access to a smartphone, computer, laptop, or tablet
  • 5\. Competent in written and spoken English and be able to provide consent

Exclusion Criteria

  • 1\. Clinical suspicion of achilles tendon rupture
  • 2\. Previous achilles tendon surgery in symptomatic leg
  • 3\. Bilateral or insertional achilles tendinopathy
  • 4\. Co\-existing foot or ankle pathology such as triognum syndrome, retro\-calanceal bursitis, superficial calcaneal bursitis, or Haglund’s syndrome
  • 5\. Systemic disease such as ankylosing spondylitis or rheumatoid arthritis
  • 6\. Confounding lower limb injury
  • 7\. Metabolic or endocrine disorders, such as type I or II diabetes
  • 8\. Corticosteroid injection in/near the achilles tendon in the last 3 months
  • 9\. Condition that prevents the patients from executing an active exercise programme
  • 10\. Previously performed strength exercise rehabilitation for achilles pain

Outcomes

Primary Outcomes

Not specified

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