Muscle Mechanical Response in Exercise.

November 24, 2023 updated by: JORGE VELAZQUEZ SAORNIL, Universidad Católica de Ávila

Muscle Mechanical Response in Active vs. Passive Resting Exercise

The muscular response on the main muscles of the propulsive phase of the upper limb in crawl has been evaluated by tensiomyography (TMG), which was carried out through three parameters: activation time (Td), contraction time (Tc) and maximum deformation (Dm).

The objective of this study is to evaluate the hypothesis of changes produced between lactic resistance training with passive rest and lactic resistance training with active rest.

For this, thirty swimmers participated, with an average age of 20 years.

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

90

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

  • Spain
    • Avila
      • Ávila, Avila, Spain, 05001
        • Jorge V Velázquez Saornil

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

  • Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

male swimmers from 18 to 25 years old with a minimum mark who swimming a croll style

Description

Inclusion Criteria:

  • Be between 18 and 25 years old.
  • have a minimum mark or have participated by ranking in a crawl event in the territorial championship of Madrid in the current season belong.
  • to the male gender.

Exclusion Criteria:

  • subjects who did not meet the minimum age and did not obtain the minimum mark and did not sign the informed consent.

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
active rest
patients taking an active rest after swimming sets
Other: Activity
patients taking an active rest after swimming sets
passive rest
patients taking a passive rest after swimming sets

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
activation time
Time Frame: 15 minutes
activation time measured by tensomiography
15 minutes
contraction time
Time Frame: 15 minutes
contraction time measured with tensomiography
15 minutes
maximum deformation
Time Frame: 15 minutes
maximum deformation measured with tensomiography
15 minutes

Collaborators and Investigators

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

Sponsor

Universidad Católica de Ávila

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

October 1, 2023

Primary Completion (Actual)

November 1, 2023

Study Completion (Estimated)

December 1, 2023

Study Registration Dates

First Submitted

November 24, 2023

First Submitted That Met QC Criteria

November 24, 2023

First Posted (Estimated)

December 4, 2023

Study Record Updates

Last Update Posted (Estimated)

December 4, 2023

Last Update Submitted That Met QC Criteria

November 24, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 24112023

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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