Changes in Grip Strength by Using Bandage Kinesio Taping

NCT ID: NCT02585037

Last Updated: 2015-10-27

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

45 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-08-31

Study Completion Date

2015-08-31

Brief Summary

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The Kinesio Taping® method, therapeutic bandage, is another feature can be used in physical therapy, aiming to muscle enhancement, weakened muscles correction, analgesia, among others, by cutaneous stimulation of mechanoreceptors. This study aims to evaluate the efficiency of the use and effects offered by Kinesio Taping® method, changes in muscle strength of grip in normal subjects for clinical application.

Detailed Description

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A sample of 45 subjects will be divided randomly into three groups (G1: muscle activation technique; G2: muscle inhibition technique; G3: Placebo Effect) aged over 18 years male or female, where it will be initially measured the strength of grip with a dynamometer Jamar® pressure. Then the Kinesio Taping® bandage will be applied in an "I" format in the wrist flexor muscles of a dominant and non-dominant limb in G1, G2, and G3 groups. Investigators will follow the application protocol suggested by method of technical. To provide the facilitation of muscle activity (G1 group) a Kinesio Taping® bandage will be applied to the muscle starting at its origin up to the location of muscle insertion. For inhibition of muscle activity (G2 group), the bandage will be placed over the muscle starting at the insertion location and ending at the muscle origin. For the control group (G3 group) the bandage will be placed from the lateral extremity to the medial axis. The measurement of grip strength was carried out in four stages: immediately before placing the Kinesio Taping®, 24 h, 48 h, and 72 h after its application. After collecting the data statistical Investigators will held the analysis of the data.

Conditions

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Hand Strength

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Kinesio Taping for facilitation

To provide the facilitation of muscle activity (G1 group) a Kinesio Taping® bandage will be applied to the muscle starting at its origin up to the location of muscle insertion. Bandage in group G1 will be applied following the protocol proposed by method of technical, which defined the direction of the bandage and an applied tension of 10% to 15% (paper off). With a dynamometer Jamar® pressure the grip strength will be messure in four stages: immediately before placing the Kinesio Taping®, 24 h, 48 h, and 72 h after its application.

Group Type EXPERIMENTAL

Kinesio Taping® bandage

Intervention Type OTHER

The Kinesio Taping® bandage will be applied in an "I" format in the wrist flexor muscles of a dominant and non-dominant limb in G1 and G2 groups.

Dynamometer Jamar® pressure

Intervention Type OTHER

The Jamar® dynamometer will be adjusted to the second position for measurement of maximal voluntary strength of handgrip. A muscle contraction period of three seconds will be performed in order to record handgrip strength.

Kinesio Taping for inhibition

For inhibition of muscle activity (G2 group), the Kinesio Taping® bandage will be placed over the muscle starting at the insertion location and ending at the muscle origin. Bandage in group G2 will be applied following the protocol proposed by method of technical, which defined the direction of the bandage and an applied tension of 10% to 15% (paper off). With a dynamometer Jamar® pressure the grip strength will be messure in four stages: immediately before placing the Kinesio Taping®, 24 h, 48 h, and 72 h after its application.

Group Type EXPERIMENTAL

Kinesio Taping® bandage

Intervention Type OTHER

The Kinesio Taping® bandage will be applied in an "I" format in the wrist flexor muscles of a dominant and non-dominant limb in G1 and G2 groups.

Dynamometer Jamar® pressure

Intervention Type OTHER

The Jamar® dynamometer will be adjusted to the second position for measurement of maximal voluntary strength of handgrip. A muscle contraction period of three seconds will be performed in order to record handgrip strength.

Kinesio Taping and Placebo

For the control group (G3 group) the Kinesio Taping® bandage will be placed from the lateral extremity to the medial axis. Bandages in the G3 group will be applied laterally to produce a similar visual effect, which control for the placebo effect, but without tension so that a muscle stimulus will be not generated. With a dynamometer Jamar® pressure the grip strength will be messure in four stages: immediately before placing the Kinesio Taping®, 24 h, 48 h, and 72 h after its application.

Group Type PLACEBO_COMPARATOR

Dynamometer Jamar® pressure

Intervention Type OTHER

The Jamar® dynamometer will be adjusted to the second position for measurement of maximal voluntary strength of handgrip. A muscle contraction period of three seconds will be performed in order to record handgrip strength.

Placebo

Intervention Type OTHER

For the control group (G3) the Kinesio Taping® bandage will be placed from the lateral extremity to the medial axis.

Interventions

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Kinesio Taping® bandage

The Kinesio Taping® bandage will be applied in an "I" format in the wrist flexor muscles of a dominant and non-dominant limb in G1 and G2 groups.

Intervention Type OTHER

Dynamometer Jamar® pressure

The Jamar® dynamometer will be adjusted to the second position for measurement of maximal voluntary strength of handgrip. A muscle contraction period of three seconds will be performed in order to record handgrip strength.

Intervention Type OTHER

Placebo

For the control group (G3) the Kinesio Taping® bandage will be placed from the lateral extremity to the medial axis.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Men or women aged greater than 18 years and with muscle / nerve integrity of upper limbs, hearing and responsive to verbal commands with understanding the information that aware and according to the study.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Mogi das Cruzes

OTHER

Sponsor Role lead

Responsible Party

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Silvia Regina M. S. Boschi

PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Silvia R. Boschi, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Mogi das Cruzes

Other Identifiers

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17119213.0.0000.5497

Identifier Type: -

Identifier Source: org_study_id

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