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Clinical Trials/NCT03196063
NCT03196063
Terminated
Not Applicable

Effectiveness of Two Exercise Protocols in the Treatment of Patients With Patellar Tendinopathy: a Randomized Controlled Trial

Universidade Cidade de Sao Paulo1 site in 1 country12 target enrollmentJuly 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patellar Tendinopathy
Sponsor
Universidade Cidade de Sao Paulo
Enrollment
12
Locations
1
Primary Endpoint
Pain intensity during rest
Status
Terminated
Last Updated
6 years ago

Overview

Brief Summary

Patellar tendinopathy is characterized by anterior pain in the knee, due to the great demand imposed on the extensor mechanism of the knee. Evidence shows that the most appropriate treatment for this condition is the conservative treatment, through strengthening with eccentric exercises. However, a recent editorial proposes a new treatment protocol based on concentric and eccentric exercises, with the initial prescription of isometric exercises. The hypothesis of this study is that the protocol is as good as the eccentric exercises, generating less pain.

Registry
clinicaltrials.gov
Start Date
July 1, 2017
End Date
December 30, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Universidade Cidade de Sao Paulo
Responsible Party
Principal Investigator
Principal Investigator

Cristina Maria Nunes Cabral

Professor

Universidade Cidade de Sao Paulo

Eligibility Criteria

Inclusion Criteria

  • patients with chronic unilateral patellar tendinopathy confirmed by the reproduction of the pain during the palpation test in the region of the lower pole of the patella
  • presence of pain for three months or more
  • both genders
  • body mass index less than 30 kg/m²
  • age between 18 and 40 years
  • practice of physical activity on a regular basis
  • pain intensity ≥ 3 points on the pain numerical rating scale in the anterior region of the knee, specifically in the region of the lower pole of the patella when performing squatting, jumping or activities with change of direction
  • score \< 80 points on the Victorian Institute of Sport Assessment-Patella (VISA-P)
  • blazine functional scale between 1 and 3

Exclusion Criteria

  • patients who have previous pain in the knee that does not correspond to patellar tendinopathy
  • previous rupture of the patellar tendon (blazin functional scale at level 4)
  • previous surgery or infiltration of the patellar tendon in the last six months
  • inflammatory diseases
  • diabetes mellitus
  • lower limbs injuries
  • other chronic pain conditions that prevent exercise, such as severe hip and knee osteoarthrosis and joint fractures.

Outcomes

Primary Outcomes

Pain intensity during rest

Time Frame: 8 weeks after randomization

This outcome will be evaluated by an 11-point scale ranging from 0 to 10, in which 0 represents "no pain" and 10 represents "pain as bad as it could be." The participant will classify his average pain in the last 7 days.

Functional capacity

Time Frame: 8 weeks after randomization

VISA-P questionnaire assesses the symptoms and disability of patients with patellar tendinopathy. It is a questionnaire with eight questions, six of them on a Likert scale, ranging from 0 to 10 points, where 0 represents the maximum severity of the disease and 10 represents no pain or limitation. Question 7 has four possible answers (0, 4, 7 and 10 points). Question 8 has a subdivision (8A, 8B and 8C), in which only one can be answered, depending on the perception of pain during sport activities, varying up to 30 points. The total score of the questionnaire varies between 0 and 100 points, with 100 points corresponding to the absence of pain or disability.

Secondary Outcomes

  • Muscular strength(8 weeks after randomization)
  • Pain intensity during rest(12 weeks and 6 months after randomization)
  • Triple hop test(8 weeks after randomization)
  • Pressure pain threshold(8 weeks after randomization)
  • Pain intensity during squat(8 weeks after randomization)
  • Functional capacity(12 weeks and 6 months after randomization)
  • Pain intensity(Eigth weeks, before and after each intervention session)

Study Sites (1)

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