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Comparative Research Among 3 Action Protocol in Other to Approach Chronic Patellar Tendinopathy

Comparative Research Among 3 Action Protocol in Other to Approach Chronic Patellar Tendinopathy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02498795
Enrollment
50
Registered
2015-07-15
Start date
2019-01-01
Completion date
2020-05-02
Last updated
2020-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tendinopathy

Keywords

Intratissue Percutaneous Electrolysis, Dry needling, Eccentric exercise, Patella

Brief summary

The accomplishment of a treatment with Intratissue Percutaneous Electrolysis of additional form to the accomplishment of eccentric exercise's program in patients with chronic patellar tendinopathy is more effective than the accomplishment of an additional treatment with dry needling or eccentric exercise's program realized of isolated form.

Detailed description

Experimental study randomized with double blind, whose purpose is to compare three protocols in those who apply different protocols of physical therapy to themselves in three groups of intervention with patients with chronic patellar tendinopathy. There take part in this study young women of both sexes, of Zaragoza and of different sports clubs of entity 18 and 40 years, that they realize of habitual form (minimum 3 times a week) a sport. All of them present chronic patellar tendinopathy.

Interventions

Every group will receive a total of 4 treatment distributed throughout 8 weeks of treatment. The program of eccentric exercises that will have to realize it in his domicile every day.

Every group will receive a total of 4 treatment distributed throughout 8 weeks of treatment. The program of eccentric exercises that will have to realize it in his domicile every day.

OTHERControl Group

Every group will receive a total of 4 treatment distributed throughout 8 weeks of treatment. The program of eccentric exercises that will have to realize it in his domicile every day.

Sponsors

Universidad San Jorge
CollaboratorOTHER
Universidad de Zaragoza
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Age understood between 18 and 40 years. * To practise any sport of habitual form. * Patients diagnosed of chronic patellar tendinopathy with a minimum of 3 months of evolution and with stable symptomatology. * Pain to the palpation of the tendon in the low pole of the knee and during the training or competition. * Punctuation of the questionnaire VISA-P under 80.

Exclusion criteria

* Patient had an operation on the knee affected in the last 6 months. * Infiltrations in the knee affected in the last 3 months. * Patient who has received pharmacological treatment or physical therapy in the last 48 hours. * Pathology with less than 3 months of evolution. * To present bilateral chronic tendinopathy. * Punctuation of the questionnaire major or equal Visa - p of 80. * Inability to apply someone of the techniques of treatment or valuation for absolute or relative contraindication.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in functionality at 8 weeks as measured by Visa-p8 weeksThis scale consists of eight questions, the first six questions of which employ an analogical visual scale in order to assign a score of 0 to 10, where 10 represents the optimum state, for the purpose of quantifying pain and function in different activities, whereas the last two questions assess the level of functionality and ability to perform physical activity.

Secondary

MeasureTime frameDescription
Quality of life by SF-360, 8 and 20 weeksHealth Survey
Thickness of the tendon, as measured by ultrasound scan0, 8 and 20 weeksTendon structure
Height of the jump0, 8 and 20 weeksJump test with a force platform
Pain, as measured by Visual Analog Scale0, 8 and 20 weeksParticipants will be explained that a score of 0 indicates the absence of pain whereas a score of 10 represents the maximum tolerable pain
Speed of the jump0, 8 and 20 weeksJump test with a force platform
Hypervascularity, as measured by ultrasound scan0, 8 and 20 weeksTendon structure
Functionality, as measured by Visa-p0 and 20 weeksThis scale consists of eight questions, the first six questions of which employ an analogical visual scale in order to assign a score of 0 to 10, where 10 represents the optimum state, for the purpose of quantifying pain and function in different activities, whereas the last two questions assess the level of functionality and ability to perform physical activity.
Concentric force of the low members0, 8 and 20 weeksJump test with a force platform

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026