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Effectiveness of Two Exercise Protocols in the Treatment of Patients With Patellar Tendinopathy

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

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03196063
Enrollment
12
Registered
2017-06-22
Start date
2017-07-01
Completion date
2018-12-30
Last updated
2019-11-15

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

Conditions

Patellar Tendinopathy

Keywords

Exercise Therapy, Heavy Slow Resistance Program, Rehabilitation

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.

Interventions

Exercises based on eccentric contractions of the quadriceps femoris muscle, using a 15º inclined plane. A serie of 15 repetitions of the squat will be performed, with the frequency of three times a week for eight weeks. The load of the exercises will be increased weekly.

OTHERModified Protocol

Protocol based on the Heavy Slow resistance program, with the addition of an isometric phase at the beginning of the protocol, and with exercises using body weight without the use of mechanotherapy.

Sponsors

Universidade Cidade de Sao Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

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.

Design outcomes

Primary

MeasureTime frameDescription
Pain intensity during rest8 weeks after randomizationThis 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 capacity8 weeks after randomizationVISA-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

MeasureTime frameDescription
Pain intensity during squat8 weeks after randomizationThis 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 patient will classify his pain during a complete isotonic unipodal squat on an inclined plane.
Pain intensityEigth weeks, before and after each intervention sessionThis 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 patient will rate the pain during rest before and after each intervention session.
Pain intensity during rest12 weeks and 6 months after randomizationThis 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.
Pressure pain threshold8 weeks after randomizationThe patient will perform 10 repetitions of the complete unipodal squat on an inclined plane and sequentially will be placed on a stretcher lying comfortably with the knee flexed at 20 degrees. The patient should indicate the point of greatest pain in the tendon, which will be marked to be the location of the tip of the algometer, and the distance to the apex of the patella will be measured to use the same point in the assessment after treatment. If the patient does not present pain in the assessment after treatment, the point standardized in the initial evaluation will be used. If the patient still presents pain, the point of greatest pain will be evaluated. For measurement, pressure will be applied until the patient experiences a mild pain sensation (pain level 1), when he will be instructed to press the algometer button to stop the test.
Muscular strength8 weeks after randomizationThe hand dynamometer will be used to measure the strength of the quadriceps femoris, hamstring, gluteus maximus, gluteus medius and lateral hip rotators.
Triple hop test8 weeks after randomizationThe patient will perform a test composed of three consecutive jumps, as far as possible, always landing on the same foot.
Functional capacity12 weeks and 6 months after randomizationVISA-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.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026