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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03515148
Other study ID # Tendon02
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 30, 2017
Est. completion date January 15, 2018

Study information

Verified date May 2018
Source Universidad Europea de Madrid
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Cryotherapy and eccentric exercise
12 weeks, 5 days/week, once a day, 2 exercise, 3 sets/execise, 15 repetition/set of eccentric exercise of foot plantar flexors First exercise with knee in extension, second exercise with knee in flexion. Previously subjects should cold their leg in ice water during sexteen minutes at a temperature of 8ºC (+/-2ºC)
Vibration and eccentric exercise
12 weeks, 5 days/week, once a day, 2 exercise, 3 sets/execise, 15 repetition/set of eccentric exercise of foot plantar flexors First exercise with knee in extension, second exercise with knee in flexion.During the exercise subjects will be subjected to vibration. Vibrations parameters: Frequency: 35Hz, Amplitude: 4 milimeters, Force: 3,9G

Locations

Country Name City State
Spain Universidad Europea Madrid

Sponsors (1)

Lead Sponsor Collaborator
Universidad Europea de Madrid

Country where clinical trial is conducted

Spain, 

Outcome

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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