Functional and Morphological Characteristics of Neck Muscles in Acrobatic Skydivers

March 8, 2021 updated by: Javier Reina Abellan, Universidad de Murcia

Functional and Morphological Characteristics of Neck Muscles in Acrobatic Skydivers: an Observational Prospective Cohort Study

An observational cohort study, following the Strengthening the Reporting of Observational Studies in Epidemiology(STROBE) guidelines.

Two groups will be examined, a group composed by spanish acrobatic skydivers and a control group composed by general physically active population(GPAP).

Study Overview

Detailed Description

Two groups will be examined for veryfing the morfology and the function of neck muscles.

The profesional group composed by spanish acrobatic skydivers and a general group composed by general physically active population(GPAP). Both groups are matched at known confounder outcomes such as: physical activity level, age, sex, body weight and history of neck pain. Frequency matching will be carried out, subjects will be matched on known confounders.

Study Type

Observational

Enrollment (Anticipated)

40

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

No older than 60 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Participants with a high level of physical activity and actualy involved in skydiving practices.

Description

Inclusion Criteria:

  • pain-free in the neck area in the last three months
  • didn't actually take any drugs that can interfere with muscle strength

Exclusion Criteria:

  • participants that not mached with the skydivers caracteristics

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
Profesional acrobatics
Profesional Acrobatic Skyedivers as the cort group
Verification of morfology and functionality of neck muscles
General active participations
Adults with meched caracteristics with the profesional acrobatics

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Anticipatory postural adjustment
Time Frame: 10 minutes
Electromyographic test in ms.The myoelectric signal will be recorded by using mDurance R system (mDurance Solutions SL, Granada). The electrodes used will be pre-gelled Ag/AgCl with a diameter of 10mm and an interelectrode distance of 20mm.
10 minutes
Isometric cervical strength
Time Frame: 10 minutes
Measured in newton with heandheld Dynamometer (model 001165, Lafayette Instrument Company)
10 minutes
Neck flexor and extensor endurance
Time Frame: 10 minutes
Measures in seconds with a stopwatch
10 minutes

Collaborators and Investigators

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

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 (Anticipated)

March 3, 2021

Primary Completion (Anticipated)

April 30, 2021

Study Completion (Anticipated)

May 30, 2021

Study Registration Dates

First Submitted

March 2, 2021

First Submitted That Met QC Criteria

March 4, 2021

First Posted (Actual)

March 5, 2021

Study Record Updates

Last Update Posted (Actual)

March 11, 2021

Last Update Submitted That Met QC Criteria

March 8, 2021

Last Verified

March 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • CE102001

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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