Skip to main content
Clinical Trials/NCT03163290
NCT03163290
Completed
Not Applicable

Effect of Two Strengthening Protocols for Lower Limbs in Patients With Patellofemoral Pain: Randomized Clinical Trial

Universidade Federal do Ceara1 site in 1 country52 target enrollmentJune 12, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patellofemoral Pain Syndrome
Sponsor
Universidade Federal do Ceara
Enrollment
52
Locations
1
Primary Endpoint
Numeric Pain Scale
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Patellofemoral Pain (PFP) is one of the most common disorders that affecting the physically active population, and its incidence is higher among women. Despite the high incidence, the etiologies of this painful syndrome are still unclear. Research has verified the influence of hip stabilizers on knee injurie and has demonstrated a deficit of strength of the hip lateral rotator, abductors and extensors muscles in patients with PFP. The aim of this study is to compare the effectiveness of strengthening the Posterolateral Hip Complex with the Anteromedial Hip Complex associated with quadriceps strengthening for pain reduction and improvement of functional capacity in patients with PFP.

Detailed Description

The physical therapy sessions will average duration of one hour, often twice a week for six weeks. The exercise intensity will be monitored by the physiotherapist as determined by the participant's ability to complete 10 repetitions for a particular exercise and its difficulty of execution perceived by the modified Borg scale (CR-10). The exercises are performed with load between 60-80% of their capacity, the load will be increased from 2 to 10% when the patient can perform 14 full repetitions in the last series. It will be set to 30 seconds of rest between reps and 2 minutes between sets of exercise. Both groups will perform prior heating exercises bike for 5 minutes with moderate intensity with the Borg scale. Then there will be one stretche repetitions held for 45 seconds of muscle groups: hamstrings, quadriceps, abductors, adductors and gastrocnemius. Thus, they will be performed strengthening exercises in extension and knee in open kinetic chain and squat. The Posterolateral Hip Complex (PLC) add hip abduction exercise, Clam exercise and external rotation exercise. Studies prior point out that these exercises are among those withhigher electromyographic activity of the gluteus medius and maximus muscles. The Anteromedial Hip Complex (AMC) add hip adduction exercise, adduction with a ring between the thighs and internal rotation exercise. The exercises will be carried out to load 60-80% of 1 repetition maximum 8-12 reps, 1-3 sets and 2-3 times a week. All exercises are performed without worsening pain and intensity of exercise will be controlled according to the perceived exertion scale of Borg.

Registry
clinicaltrials.gov
Start Date
June 12, 2017
End Date
March 12, 2019
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Gabriel Peixoto Leão Almeida

Professor

Universidade Federal do Ceara

Eligibility Criteria

Inclusion Criteria

  • Practicing physical activity for at least 3 times a week for at least 30 minutes;
  • Pain localized specifically around the patellofemoral joint, pain reproduced or reported in at least two of the following criteria: up or down stairs, squatting, kneeling, sitting for a long time, isometric contraction of the quadriceps, jumping, running and pain on palpation of the lateral and / or medial facet of the patella;
  • Report pain of insidious onset and lasting at least three months;
  • Pain at least three in the Numerical Pain Scale during the last week;
  • Report a maximum of 86 points on the Anterior Knee Pain Scale (maximum = 100 points).

Exclusion Criteria

  • Previous surgery on the hip, knee, ankle and / or spine;
  • History of patellar dislocation;
  • Clinical evidence of knee instability (anterior and posterior drawer test, Lachman, varus and valgus stress);
  • Meniscal lesions or intra-articular lesions;
  • Evidence of edema;
  • Osgood-Schlatter syndrome or Sinding-Larsen-Johansson;
  • Patellar tendinopathy;
  • Chondral lesion;
  • Osteoarthritis;
  • Muscle or joint injuries to the hip.

Outcomes

Primary Outcomes

Numeric Pain Scale

Time Frame: Six weeks

Pain was assessed by use of an 11-point Numeric Pain Scale, where 0 corresponded to no pain and 10 corresponded to worst imaginable pain. to worst imaginable pain.

Anterior Knee Pain Scale

Time Frame: Six weeks

Anterior Knee Pain Scale assesses functional capacity and pain level during functional and specific activities for patients with PFP. This scale was translated and culturally adapted to the Brazilian Portuguese language,10 and the score ranges from 0 (worst) to 100 (best).

Secondary Outcomes

  • Numeric Pain Scale(Six months)
  • Anterior Knee Pain Scale(Six months)
  • Numeric Pain Scale on Step Down Test(Six weeks)
  • Dynamic Knee Valgus on Frontal Plane Projection Angle(Six weeks)
  • Global Effect Perception Scale(Six months)
  • Muscle strength(Six weeks)

Study Sites (1)

Loading locations...

Similar Trials