Achilles Tendinopathy Clinical Trial
Official title:
Effectiveness of Eccentric Exercise With a Vibration Program Versus Cryotherapy in Rectus Abdomini Muscle Thickness and Inter-recti Distance in Patients With Chronic Mid Portion Achilles Tendinopathy: A Randomized Clinical Trial
Verified date | May 2018 |
Source | Universidad Europea de Madrid |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to determinate de efectiveness of eccentric exercise combined
with vibration or cryotherapy in achilles tendinopathy and its effects on the anterior rectus
abdominis muscle.
The investigators hypothesis is the combined eccentric exercise with vibration get better
results than cryotherapy with eccentric exercise in rectus abdominis muscle parameters.
Status | Completed |
Enrollment | 61 |
Est. completion date | January 15, 2018 |
Est. primary completion date | December 15, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
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 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 |
Country | Name | City | State |
---|---|---|---|
Spain | Universidad Europea | Madrid |
Lead Sponsor | Collaborator |
---|---|
Universidad Europea de Madrid |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Inter-recti distance | Ultrasound diagnosis | 3 months | |
Primary | Rectus abdominis thickness | Ultrasound diagnosis | 3 months |
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