Influence of Wrist Taping on Handgrip Strength in Crossfit Athletes

August 25, 2021 updated by: Vita Care

Influence of Wrist Taping on Handgrip Strength in Crossfit Athletes - Crossover Randomized Controlled Trial

The idea that the use of a wristband can increase the grip strength is old, but without systematic scientific evidence. Most Crossfit practitioners wear wrist bands during training because it is believed that the wristband increases the grip strength of the hand. The aim of this study is to to analyze the influence of the use of the wristband on the maximum force value and on the dynamic resistance of hand hold. A simple blind randomized cross-over trial will be performed.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

54

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • SP
      • Sao Paulo, SP, Brazil, 01239-040
        • Instituto Vita

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • be an amateur practitioner of the Crossfit modality with at least 6 months of regular sports practice (at least 4 times a week)
  • between 18-40 years old
  • agree to participate in the study and sign the informed consent form (ICF).

Exclusion Criteria:

  • active wrist/ arm injury or pain on the day of the test (pain score greater than 3 in 10 for both shoulder, forearm, wrist and / or hand on the VAS pain scale)
  • history of wrist injury (especially fracture or ligament injury)
  • previous wrist surgery

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Sham Comparator: Sham first (group 1)
Performs the first round of test with the sham comparator than with the experimental wrist taping
Wrist taping as used as standard in CrossFit practice
Experimental: Wrist taping first (group 2)
Performs the first round of test with the experimental wrist taping than with the sham comparator
Wrist taping as used as standard in CrossFit practice

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Grip
Time Frame: 0 minutes; 5 minutes
Mean of the first 3 hand pressures (kg) measured by hand dynamometer
0 minutes; 5 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Endurance
Time Frame: 0 minutes; 5 minutes
Percentage (%) of strength measured in the last 3 movements in relation to the first 3 movements
0 minutes; 5 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Study Director: Luis Marchi, PhD, Instituto Vita

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2020

Primary Completion (Actual)

February 1, 2021

Study Completion (Actual)

February 2, 2021

Study Registration Dates

First Submitted

February 23, 2021

First Submitted That Met QC Criteria

March 2, 2021

First Posted (Actual)

March 4, 2021

Study Record Updates

Last Update Posted (Actual)

August 26, 2021

Last Update Submitted That Met QC Criteria

August 25, 2021

Last Verified

August 1, 2021

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 103

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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