NCT02501915

Brief Summary

The Kinesio Taping (KT ) method was developed more than thirty years ago in order to cause sensory effects through the epidermis and dermis, generating a variety of physiological effects in other systems. Clinical effects are well known levels in muscle, neurological system, injuries, inflammation, edema, among other physiological effects are thus largely in the theoretical framework. Objectives: The aim of this study is to evaluate the Electromyographic (EMG), Electroencephalographic (EEG), muscle temperature and flexibility effects with the Rectus Femoral muscle KT application. Methods: This is a pilot study with six subjects in which they were divided into two groups, A and B. Group A received the application of KT from muscle Origin to Insertion and group B Insertion to Origin, with both groups taped the non-dominant limb and the dominant limb was used as control group. The first application was conducted at 0% and the second with 75 to 100% tension. Evaluations were performed before the first application, immediately and 24 hours later. After this last evaluation, was withdrawn taping, evaluated without taping, reapplied 75 to 100 % of rated voltage and in sequence. The sixth last review was conducted 24 hours after this last application. Before every application a specific vibration was performed on the patellar tendon in order to trigger a neurophysiological imbalance rectus femoral.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at P25-P50 for phase_1

Timeline
Completed

Started Feb 2014

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2014

Completed
11 days until next milestone

First Submitted

Initial submission to the registry

February 12, 2014

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2014

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2015

Completed
7 months until next milestone

First Posted

Study publicly available on registry

July 17, 2015

Completed
Last Updated

July 21, 2015

Status Verified

July 1, 2015

Enrollment Period

10 months

First QC Date

February 12, 2014

Last Update Submit

July 17, 2015

Conditions

Keywords

Muscle

Outcome Measures

Primary Outcomes (1)

  • Muscle Activity

    Group A (n= 15) received the application of KT from muscle (Rectus femoral) Origin to Insertion, Group B (n= 15) from insertion to origin at the non dominant limb, and the dominant limb will be used as control group. The Eletromiography/ EMG (mV) will be measure during an maximum isometric voluntary contraction.

    The outcome will be evaluated 24 hours after the intervention

Secondary Outcomes (1)

  • Neurologic Activity

    The outcome will be evaluated 24 hours after the intervention

Other Outcomes (2)

  • Muscle Stregth

    The outcome will be evaluated 24 hours after the intervention

  • Local Temperture

    The outcome will be evaluated 24 hours after the intervention

Study Arms (2)

Kinesio Taping (GROUP A)

EXPERIMENTAL

Received the application of KT from muscle Origin to Insertion

Device: Kinesio Taping

Kinesio Taping (GROUP B)

EXPERIMENTAL

received the application of KT from muscle Insertion to Origen

Device: Kinesio Taping

Interventions

Group A received the application of KT from muscle Origin to Insertion and group B Insertion to Origin, with both groups taped the nondominant limb and the dominant limb was used as control group. Diferent tensions will be applied with the tape to see its possible different affect in the outcomes.

Also known as: Kinesio Tex Tape FP (Finger Print)
Kinesio Taping (GROUP A)Kinesio Taping (GROUP B)

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Individuals who have authorized the evaluation procedure and through the Term Informed Consent;
  • Individuals male and female of any race, duly enrolled in some college course of Universidade Salgado de Oliveira aged between 18-50 years old;
  • Healthy subjects without disorders of locomotion without injury history the last 6 months in the lower limbs.

You may not qualify if:

  • They are considered unfit for research individuals who do not meet the requirements listed above ;
  • Individuals who have higher body mass index (BMI ) to 24.99, as the concentrated presence of fat on muscles can limit the effect of bracing;
  • Individuals with musculoskeletal disorders and referring pain. Since there report that the pain and dysfunction of movement restricted range of motion and function muscular18 ;
  • Individuals who possess too much on the thigh in which prevent proper attachment of bracing and the EMG electrode , or who refuse to perform the trichotomy .
  • they show taping allergy ( an allergy test by putting a small bandage on the skin will be held and observed for 24 hours ) ;
  • Patients with any contraindication how physical activity according to the guideline of the American College of Sports Medicine (ACSM , 1995), nerve root involvement, cardiorespiratory conditions and pregnancy .

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (1)

  • Lemos TV, Junior JRS, Santos MGRD, Rosa MMN, Silva LGCD, Matheus JPC. Kinesio Taping effects with different directions and tensions on strength and range of movement of the knee: a randomized controlled trial. Braz J Phys Ther. 2018 Jul-Aug;22(4):283-290. doi: 10.1016/j.bjpt.2018.04.001. Epub 2018 Apr 14.

MeSH Terms

Conditions

Myositis

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal DiseasesNeuromuscular DiseasesNervous System Diseases

Study Officials

  • João V Matheus, PHD

    Universidade de Brasilia

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physical Therapy Professor at Universidade Estadual de Goias; Phd Student at Universidade de Brasília

Study Record Dates

First Submitted

February 12, 2014

First Posted

July 17, 2015

Study Start

February 1, 2014

Primary Completion

December 1, 2014

Study Completion

January 1, 2015

Last Updated

July 21, 2015

Record last verified: 2015-07