MedPath

Eccentric Training and Cryotherapy Vs Eccentric Training and Whole Body Vibration in Achilles Tendinopathy

Not Applicable
Completed
Conditions
Achilles Tendon
Tendinopathy
Interventions
Other: Vibration and eccentric exercise
Other: Cryotherapy and eccentric exercise
Registration Number
NCT03029910
Lead Sponsor
Universidad Europea de Madrid
Brief Summary

The purpose of this study is to determine the effectiveness of eccentric exercise combined with vibration or cryotherapy in Achilles tendon pathology.

The investigators hypothesis is that the combined eccentric exercise is better than the results presented by the exclusive eccentric exercise.

This intervention differs from the classic studies in that we maintain the intensity throughout the treatment.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
132
Inclusion Criteria
  • Sports people
  • Positive initial ultrasound diagnosis
  • Presence of degenerative changes at achilles mid portion
  • Chronic Achilles tendon pain, (3/10 VAS)
  • Pain when walking or running of Achilles tendon, (3/10 VAS)
  • Pain in load in plantar flexion of Achilles tendon, 3/10 VAS)
  • Pain in palpation of Achilles, (3/10 VAS)
  • Morning Stiffness

Inclusion Criteria Healthy pople:

  • Sports people
  • Negative initial ultrasound diagnosis
  • No syntomp of achilles tendinophaty
Exclusion Criteria
  • Receive physical, orthotic or physiotherapeutic treatment
  • Asociated low back pain, ankle/knee/hip injury that may affect the study
  • Previous injury or surgery of Achilles tendon.
  • Pathologies that may limit the joint of ankle
  • Pregnancy
  • Obesity
  • Patients with diabetes and/or other endocrine or metabolic pathologies or neurologic pathologies
  • Patients diagnosed with cardiovascular disease
  • Subjets diagnosed with familiar hypercholesterolemia and/or presence of xanthomas or with hyperuricemia
  • Patients who have received renal transplantation
  • Subjects who have suffered retinal detachment
  • Subjects who have received oral contraceptives, statins, corticoids or hormone replacement therapy in the last six months
  • Subjects who have received treatment wiht fluoroquinolones in the last two years
  • Subjects who have received treatment with AINE's in the last four weeks

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Vibration and eccentric exerciseVibration and eccentric exercise-
Cryotherapy and eccentric exerciseCryotherapy and eccentric exercise-
Primary Outcome Measures
NameTimeMethod
Change at Achilles Tendon Cross Sectional Area3 months

Ultrasound diagnosis.

Change at Achilles Tendon Thickness3 months

Ultrasound diagnosis.

Secondary Outcome Measures
NameTimeMethod
Differences between healthy volunteers and volunteers with Achilles tendinopathy2 weeks

Ultrasound diagnosis

Trial Locations

Locations (1)

Universidad Europea

🇪🇸

Madrid, Spain

© Copyright 2025. All Rights Reserved by MedPath