tendinopathy
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants aged between eighteen and fifty years with medical diagnosis of patellar tendon or tendon tendon disease for at least 3 months and have a VISA score (P and A) of less than 80 points without treatment for at least 3 months and signed the term of free and informed consent.
Exclusion criteria
Exclusion criteria: Individuals with neurological disorders that affect cognitive behavior and pain perception; conditions in the knee or ankle region (such as rheumatoid arthritis; osteoarthritis or fractures) that make it impossible to perform the assessments or protocol proposed; pregnancy; previous surgical procedure in the tendon; use of non-steroidal anti-inflammatory drugs (NSAIDs) during the last 2 weeks; injection of corticosteroids; diabetes mellitus and uncontrolled hypertension.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improve pain and function analyzed by VISA-P Questionnaire with an increase of 13 point at least at the end of the study. | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain improvement measured through NRS-11 with a 2-point decrease in pain intensity in the activity that causes the most pain at the end of the study | — |
Countries
Brazil
Contacts
Universidade Federal de São Paulo