Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02841384
Other study ID # Mcconnelltaping
Secondary ID
Status Completed
Phase N/A
First received July 1, 2016
Last updated November 28, 2017
Start date July 1, 2016
Est. completion date May 3, 2017

Study information

Verified date November 2017
Source Universidade Estadual de Londrina
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Introduction: Patellofemoral pain syndrome (PFPS) is related to the previous sore knee, change functionality and postural control deficits. One of the possibilities for pain control and better positioning of the patella is the rigid bandage patellar widely used by clinicians and researchers.

Objective: To evaluate the effect of rigid patellar bandage on postural control, pain and function in sedentary women with PFPS.

Methods: The sample will be composed of 30 volunteers, sedentary, between 18 and 55 years; randomized group Bandage Functional Rigid (n = 15) and Banding Placebo (n = 15). All fill the Personal Data Sheet, Visual analog scale Pain Questionnaire Previous Knee Pain Scale; and will be submitted to analysis of postural control (static and dynamic) and carry out the test and sit up in pre conditions and post application of the bandage.

Hypothesis: Expected to observe the effect of rigid patellar bandage in pain, function and postural control in sedentary women with PFPS.


Description:

This is a randomized controlled trial and blind in the exercise area, postural control and biomechanics.

The subjects with a clinical diagnosis of PFPS will be allocated in two groups: PFPS group with rigid bandage patella (n = 15) and PFPS group with placebo (n = 15).

Procedures: The subjects with a clinical diagnosis of PFPS, will be forwarded to the evaluation protocols. The data collections will be held at University Hospital Physiotherapy Division of the State University of Londrina. Individuals respond to a questionnaire to characterize the sample, EVA and fill the patellofemoral disorders Scale (AKPS).

Data Collection Protocol: will be held to familiarize themselves with the equipment and tests to be used on the force platform and test sitting and standing, voluntary is inserted in one of the groups (PPS + B or PPS + P) through randomisation previously established by www.random.org and stored in opaque and sealed envelopes.

Following the participants carry out, random and drawn at the time way, the static and dynamic tests on the force platform:

Static: The volunteers will stay 30 seconds in one-leg position of the lower limb with pain with the knee flexed and contralateral suspended to about 90; the test will be performed three times, with one minute of sitting home. Participants will be instructed to keep aligned and torso upright during the test and stay as long as possible with most of the plantar region touching the ground. Will be targeted to fix the look upon in a pre-established and pasted on the wall point.

Dynamic Squat: The volunteers will perform three consecutive repetitions of squat exercise, controlled between about 0 ° to 45 ° of knee flexion in the lower limb with pain. The contralateral leg should be suspended and flexed to 90 °, the activity will be performed three times, with one minute rest in the sitting position between each repetition. Participants will be instructed to keep aligned and torso upright during the test and stay as long as possible with most of the plantar region touching the ground. Will be targeted to fix the look upon in a pre-established and pasted on the wall point.

Dynamic Up and Down Stairs: The force platform will be positioned at 20 cm from the ground on a wooden structure. The front is combined with a second step, also with 20 cm high from the first step, simulating a staircase with two steps of 20 cm each. Voluntary perform the functional activity of climbing the two steps, starting the first step with the leg with pain to support the platform. The activity will be carried out three consecutive times, with rest of a seated minute, and then the voluntary hold the decline in two steps, with lower limb support with pain on the platform, also performed by three consecutive times.

The average of the three repetitions of each activity (static and dynamic) will be used for postural control analysis (COP parameters) for each variable to be analyzed.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date May 3, 2017
Est. primary completion date December 30, 2016
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- Clinical diagnosis of patellofemoral dysfunction issued by a specialist orthopedic knee and provide anterior knee pain of 3 or more on the Visual Analogue Scale (VAS) for a minimum of 8 weeks prior to evaluation;

- Previous retropatellar pain or knee, for at least 3 of the following: up / down stairs, squatting, running, kneeling, sitting for long periods and insidious onset of symptoms unrelated to trauma.

Exclusion Criteria:

- History of severe / traumatic knee injury, surgery history in the locomotor system;

- Patellar luxation history; clinical evidence of meniscus injury; ligamentous instability; patellar tendinitis.

- Presence of neurological, cardiovascular or rheumatologic diseases; pregnancy; diabetes,

- Abnormal sensitivity in the plantar;

- Medication and / or therapy in the last six months and hypersensitivity or allergy to tape.

Study Design


Intervention

Other:
taping patellar McConnell
Taping patellar McConnell: Lateralization correction of the patella with self-adhesive rigid bandage Johnson® positioned lateral border of the patella to the medial condyle of the femur, allowing the lifting of the medial border of the patella and stretching of the knee lateral structures.
Placebo taping
Placebo taping through vertical application of patellar rigid taping, with the knee in flexion without medialization of the patella.

Locations

Country Name City State
Brazil university hospital of the State University of Londrina Londrina Paraná

Sponsors (1)

Lead Sponsor Collaborator
Universidade Estadual de Londrina

Country where clinical trial is conducted

Brazil, 

References & Publications (2)

Felicio LR, Masullo Cde L, Saad MC, Bevilaqua-Grossi D. The effect of a patellar bandage on the postural control of individuals with patellofemoral pain syndrome. J Phys Ther Sci. 2014 Mar;26(3):461-4. doi: 10.1589/jpts.26.461. Epub 2014 Mar 25. — View Citation

Lee SE, Cho SH. The effect of McConnell taping on vastus medialis and lateralis activity during squatting in adults with patellofemoral pain syndrome. J Exerc Rehabil. 2013 Apr;9(2):326-30. doi: 10.12965/jer.130018. Epub 2013 Apr 25. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary change the balance after the intervention by force platform It will be measured the oscillations through various force platform variables before and after the intervention (taping or placebo, depending on the group) to see if there is change in the balance after the implementation of these interventions. before and immediately after the intervention
See also
  Status Clinical Trial Phase
Completed NCT04538508 - Radiofrecuency and Supervised Exercise Versus Supervised Exercise in the Treatment of Patellofemoral Pain Syndrome. N/A
Completed NCT03685812 - Validity and Reliability of Autocad Software Assessment of JPS in PFPS
Completed NCT02873143 - 5 Year Follow-up of Adolescents With Knee Pain N/A
Active, not recruiting NCT02114294 - Hip Strengthening Versus Quadriceps Based Training for Patellofemoral Pain Syndrome N/A
Completed NCT02243332 - Dynamic Quadriceps Muscle Stimulation for Treatment of Patellofemoral Pain N/A
Completed NCT01696162 - Conventional Home Exercise Programs Versus Electronic Home Exercise Versus Artificial Intelligence "Virtual Therapy" for Anterior Knee Pain N/A
Completed NCT01434966 - Changes in Quadriceps Function Following Local or Distant Interventions in Individuals With Patellofemoral Pain N/A
Not yet recruiting NCT05327569 - The Efficacy of Myofascial Chain Release Techniques in Patients With Patellofemoral Pain Syndrome. N/A
Completed NCT06060730 - Measurement Properties of the Turkish Version of the Patellofemoral Pain and Osteoarthritis Subscale of the KOOS
Completed NCT03281421 - Immediate Effects of Ankle Mobilization on Dorsiflexion Range of Motion in Women With Patellofemoral Pain. N/A
Recruiting NCT06130696 - Clamshell Exercise in Patellofemoral Syndrome. N/A
Completed NCT03201133 - Clinical Subgroups in Patellofemoral Pain Syndrome
Completed NCT05959148 - Adjuvant Effects of Monochromatic Infrared Energy in Rehabilitation of Adolescents With Patellofemoral Pain Syndrome N/A
Completed NCT02646579 - Effects of Dry Needling Using Spinal and Peripheral Sites Versus Peripheral Sites Only N/A
Completed NCT00978003 - Vasti Control of Patellofemoral Kinematics in Asymptomatic Volunteer
Not yet recruiting NCT04631614 - Addition Effect of the Ankle Manual Therapy to Muscle Strengthening Exercise in Women With Patellofemoral Pain N/A
Not yet recruiting NCT05383781 - Effect of Short Foot Exercise in Treatment of Patients With Patellofemoral Pain Syndrome N/A
Not yet recruiting NCT05083897 - Effect of Hip Adductors Isometric Contraction on Knee Extensors Isokinetic Torque in Patellofemoral Pain Syndrome
Withdrawn NCT03157271 - The Addition of Dry Needling in the Treatment of Patients With Patellofemoral Pain Syndrome N/A
Enrolling by invitation NCT02548988 - Selective Neuromuscular Electrical Stimulation on VMO N/A