Patellar Taping on Proprioceptive Exercises in Young Women With Patellofemoral Pain Syndrome

NCT ID: NCT02322515

Last Updated: 2015-12-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-01-31

Study Completion Date

2015-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The relevance of this study is to determine the effects of a patellar taping on muscle activation of the vastus medialis oblique (VMO), vastus lateralis (VL) and gluteus medius (GM) during different proprioceptive exercises frequently utilized in rehabilitation program.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The purpose of this study is to assess the role of the patellar taping on muscle activation during seven proprioceptive exercises in women with the patellofemoral pain syndrome.

Forty voluntary young women (from 18 to 35 years) with three or more clinical symptoms of patellofemoral pain syndrome will be recruited. The participants will answer a clinical questionnaire in regard to knee pain and a specific patellofemoral questionnaire titled: the Anterior Knee Pain Scale (AKPS). All participants will sign an informed consent form approved by the North of Parana University Ethics Committee for Research on Human Subjects. The sample will be randomized in two groups: (G1) the experimental group that will use a rigid patellar taping (n = 20) for the correction in lateralization of the patella and stabilization of the knee. The lateral stabilization will be made with self-adhesive taping positioned in the lateral border of the patella and tensioned in relation to the medial portion of the femur condyle, which allows an edge of the medial board patella and a stretching of lateral structures of the knee. All procedure will follow the recommendation from McConnell studies with regard to the patellar femoral syndrome; and (G2) the placebo group that will use a rigid patellar taping (n = 20), but without no correction of lateralization of the patella and/or stabilization of the knee. The taping will be placed incorrectly such as in the vertical position of knee and without any tension or traction around structures and patella. A computer will be used to generate the randomization sequence of the participants. The allocation will be printed in cards by sequentially numbered in opaque envelopes.

Before performing the exercises, a maximum voluntary isometric contraction will be performed for the knee extensor muscles (e.g. specifically the VMO and VL) and hip abductor muscles (e.g. GM) in order to normalize the signal EMG for determining of the level muscular activity during each exercise, with the correct taping and/or placebo. All participants, after randomization, will perform seven proprioceptive exercises on one leg-stance position in different surfaces: 1) static position in force platform, 2) dynamic in flexion-extension knee on a force platform, 3) anteroposterior sway on rectangular rocker board, 4) mediolateral sway on rectangular rocker board, 5) unipodal standing on a swing apparatus, 6) unipodal standing on a mini-trampoline, and 7) unipodal standing on bosu balance ball. Each exercise has a time of 15 seconds performance, while sway centre of pressure parameters will be computed (exercise #1 and #2), and EMG surface will recording (VMO, VL, GM) for all seven. First, one baseline measure (without taping) will be performed and immediately after with the use of taping (intervention or placebo).

An ANOVA two-way will be performed to compare the two groups (G1 and G2) and two times (before and immediately after with taping) and the effects of interaction (Groups x Times). The size effect also will be computed to determine the rate of the changes observed.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Anterior Knee Pain Syndrome

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Intervention Taping

The experimental group will use a rigid patellar taping (G1, n = 22) for the correction of lateralization of the patella and stabilization of the knee. The lateral stabilization will be made with self-adhesive taping positioned in the lateral border of the patella and tensioned in relation to the medial portion of the femur condyle, which allows an edge of the medial board patella and a stretching of lateral structures of the knee. All procedure will follow the recommendation from McConnell studies with regard to the patellar femoral syndrome.

Group Type EXPERIMENTAL

Intervention taping

Intervention Type OTHER

A rigid patellar taping will be used for the correction in lateralization of the patella and more stabilization of the knee.

Placebo Taping

The placebo group will use a rigid patellar taping (G2, n = 22), but without no correction of lateralization of the patella and/or stabilization of the knee. The taping will be placed incorrectly such as in the vertical position of knee and without any tension or traction around structures and patella.

Group Type PLACEBO_COMPARATOR

Placebo Taping

Intervention Type OTHER

A rigid patellar taping will be used in the vertical position and without no correction in lateralization of the patella and/or stabilization of the knee.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Intervention taping

A rigid patellar taping will be used for the correction in lateralization of the patella and more stabilization of the knee.

Intervention Type OTHER

Placebo Taping

A rigid patellar taping will be used in the vertical position and without no correction in lateralization of the patella and/or stabilization of the knee.

Intervention Type OTHER

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Patellar taping Sham taping

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* anterior or retropatellar knee pain on at least two of the following activities: prolonged sitting, stairs, squatting, running, kneeling, and hopping/jumping,
* pain on patellar palpation,
* pain while stepping down from a 25-cm step or during a double leg squat,
* symptoms for at least 1 month, average pain level of 3 cm or more on a 10-cm VAS.

Exclusion Criteria

* signs or symptoms of other pathology including coexisting pathology, a recent history (within 3 months) of knee surgery,
* history of patellar dislocation/subluxation, or clinical evidence of meniscal lesion, ligamentous instability, traction, apophysitis around the patellofemoral complex, patellar tendon pathology, chondral damage, osteoarthritis, or referred pain from the spine, features that could affect the implementation of the trial,
* previous experience with patellar taping, an inability to attend a physical therapy clinic for a 6-wk treatment program,
* allergic reaction to adhesive tape,
* pregnancy, and an inability to understand the experimental protocol.
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Universidade Estadual de Londrina

OTHER

Sponsor Role collaborator

Universidade Norte do ParanĂ¡

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Rubens Alexandre da Silva Jr

Titular professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Rubens A DA SILVA, PhD

Role: PRINCIPAL_INVESTIGATOR

Universidade Norte do ParanĂ¡

References

Explore related publications, articles, or registry entries linked to this study.

Cowan SM, Bennell KL, Crossley KM, Hodges PW, McConnell J. Physical therapy alters recruitment of the vasti in patellofemoral pain syndrome. Med Sci Sports Exerc. 2002 Dec;34(12):1879-85. doi: 10.1097/00005768-200212000-00004.

Reference Type BACKGROUND
PMID: 12471291 (View on PubMed)

McCONNELL J. The management of chondromalacia patellae: a long term solution. Aust J Physiother. 1986;32(4):215-23. doi: 10.1016/S0004-9514(14)60654-1.

Reference Type BACKGROUND
PMID: 25025219 (View on PubMed)

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.

Reference Type BACKGROUND
PMID: 24278879 (View on PubMed)

Araujo CG, de Souza Guerino Macedo C, Ferreira D, Shigaki L, da Silva RA. Mcconnell's patellar taping does not alter knee and hip muscle activation differences during proprioceptive exercises: A randomized placebo-controlled trial in women with patellofemoral pain syndrome. J Electromyogr Kinesiol. 2016 Dec;31:72-80. doi: 10.1016/j.jelekin.2016.09.006. Epub 2016 Sep 21.

Reference Type DERIVED
PMID: 27693990 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Unopar-Rubens

Identifier Type: -

Identifier Source: org_study_id