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Completed

NCT Number: NCT03103048

Application of Different Techniques of Elastic Bandage

This study will be featured as a randomized controlled. As the dependent variable, was considered isometric grip manual force. As independent variable, the presence or absence of forearm bandage in the fist flexor region of the volunteers.

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Key information

Age range

18 year–38 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Terigi Augusto Scardovelli

Mogi das Cruzes, São Paulo, 08615120, Brazil

About this study

This study is directed to the population of students at the University of Mogi das Cruzes (UMC), and will take part of this study forty volunteers, twenty men and twenty women, aged from eighteen and thirty-eight years old. Will be selected and included volunteers who do not do physical professional activity with upper members, which have no symptom of pain skeletal muscle in the upper members, which have not undergone any type of surgery in the region of the forearm and hand of both members. Will be excluded the volunteers who have injuries, joint injuries, neuromuscular disorder or those who have knowledge of own vestibular or neurological changes. Will also be excluded from study volunteers who do not agree to participate after reading and understanding of informed consent in accordance with resolution 466/12 of the National Ethics Committee and Research. The data acquisition interface will be acquired by an electromyography e a standard of strentgh will maintened in forty Newtons assured by an electronic dynamometer for tests of palmar prehension without and with bandages. The volunteers will not know what kind of intervention will pass. After each application before testing, their both forearms will be covered with a protection. The researcher and the volunteers will not know the tests order.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Who do not do physical professional activity with upper members;
  • Who have no symptom of pain skeletal muscle in the upper members;
  • Who have not undergone any type of surgery in the region of the forearm and hand of both members;
  • Consent form signed by the volunteer.

Exclusion criteria

  • Having less than 18 years old;
  • Having more than 38 years old;
  • To present some compromise skeletal muscle in the upper members;
  • Who do not want take part in the research;
  • Who do not signed consent form as volunteer.

Treatment and study plan

Without bandages

Diagnostic Test

All volunteers will be held the grasping force measurements without application of elastic adhesive bandage or micropore

With placebo

Diagnostic Test

All volunteers will be held the grasping force measurements with application of micropore (placebo) on his forearm in both upper members

With bandage

Diagnostic Test

All volunteers will be held the grasping force measurements with application of bandage without tension in the forearm in both upper members

With tensioned bandage

Diagnostic Test

All volunteers will be held the grasping force measurements with application of bandage with twenty five percent tensioned on the forearm in both upper members

Primary outcomes

  1. Efforts

    Time frame: 15 minutes

    Thru palmar prehension there will be data acquisition interface by an electromyography e a standard of strentgh maintened in 40 Newtons assured by an electronic dynamometer for tests of palmar prehension, with and without elastic adhesive bandages in the region of flexor muscle of fist.

Sponsors and collaborators

Lead sponsor

University of Mogi das Cruzes

Other

Registry information

Official study title

Application of Different Techniques of Elastic Bandage: Quantification Electromyographic at the Isometric Effort of Flexor Muscle of Fist

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Apr 6, 2017
Registry last updated
May 18, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.