Motor Imagery and Muscle Architecture

November 22, 2022 updated by: Murat EMİRZEOĞLU, Hacettepe University

The Effects of Motor Imagery and Action Observation-Based Plyometric Training on Vastus Lateralis and Biceps Femoris Muscle Architectures of Adolescent Football Players

The aim of this study is to examine the effects of plyometric training on biceps femoris longus (BFl) and vastus lateralis (VL) muscle architecture in healthy football players. Individuals will be randomly placed into training and control groups. Measurements of muscle architecture will be taken bilaterally from BFl and VL muscles by means of an ultrasound device. Functional performance will be evaluated with the single leg jump test. Following the initial evaluations, individuals in the training group will receive plyometric training. Evaluations of muscle architecture and functional performance will be taken again from the individuals in the training and control groups at the end of the 4th and 8th weeks. The received ultrasound images will be calculated through the MicroDicom software. In-group and between-group comparisons will be analyzed using the Statistical Package for the Social Sciences program and appropriate tests.

Study Overview

Status

Recruiting

Conditions

Detailed Description

The aim of this study is to examine the effects of plyometric training on biceps femoris longus (BFl) and vastus lateralis (VL) muscle architecture (fiber length, penation angle and muscle thickness) in healthy football players. Individuals will be randomly placed into two different groups, the training group and the control group. Imagery ability, self-efficacy and motivation will be evaluated with various questionnaires and scales in order to compare the homogeneity of the groups. Measurements of muscle architecture will be taken bilaterally from BFl and VL muscles by means of an ultrasound device. Functional performance will be evaluated with the single leg jump test. Following the initial evaluations, individuals in the training group will receive plyometric training consisting of ten different exercises for 8 weeks, 3 sessions per week. In this training, individuals will not participate in a real plyometric training. Volunteers will watch videos to be prepared (action observation) and imagine them performing those exercises (motor imagery). All trainings will be given on the basis of telerehabilitation via distance education tools. Cognitive fatigue at the beginning and end of the session; at the end of each session, the technical quality and efficiency of the training will be evaluated. Evaluations of muscle architecture and functional performance will be taken again from the individuals in the control and training groups at the end of the 4th and 8th weeks. The received ultrasound images will be calculated through the MicroDicom software. In-group and between-group comparisons will be analyzed using the Statistical Package for the Social Sciences program and appropriate tests.

Study Type

Interventional

Enrollment (Anticipated)

40

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 Contact

Study Locations

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

12 years to 19 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Be in the 12-19 age range
  • Being actively playing football as licensed

Exclusion Criteria:

  • Those who have undergone lower extremity surgery
  • Those with a history of second and third degree strain type injuries in the hamstring and quadriceps muscle groups
  • Those with a history of injury to the lower extremity in the last two years
  • Those with a history of congenital, neurological, orthopedic, rheumatological and cardiopulmonary pathologies or anomalies,
  • Those with a diagnosis of systemic disease (diabetes, blood pressure, thyroid diseases, etc.)
  • Those with acute infection and pain
  • Those with a diagnosis of joint instability
  • Those with a body mass index of 30 and above
  • Those who received energy supplements or ergogenic aids during the study or during the 6-month period before the study
  • Those who do not follow the research protocol

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Plyometric Training Group
Individuals in the plyometric training group will receive plyometric training. In this training, individuals will not participate in a real plyometric training. Volunteers will watch videos to be prepared (action observation) and imagine them performing those exercises (motor imagery). All trainings will be given on the basis of telerehabilitation via distance education tools.
Plyometric training consisting of ten different exercises [vertical unilateral and bilateral counter movement jump, horizontal unilateral and bilateral counter movement jump, drop jump (30 cm), squat jump, step-hop (20 cm), 180 degree rotation in transverse plane, frontal plane hurdle jump (20 cm) and sagittal plane hurdle jump (20 cm)] for 8 weeks, 3 sessions per week. Individuals will not participate in a real plyometric training. Volunteers will watch videos to be prepared (action observation) and imagine them performing those exercises (motor imagery)
Active Comparator: Control Group
Athletes in this group will continue their routine training programs like the athletes in the plyometric training group.
Routine football trainings

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle Architecture Change-1
Time Frame: Before, at the end of the fourth week and the eighth week
Fiber length of the vastus lateralis and biceps femoris longus muscles
Before, at the end of the fourth week and the eighth week
Muscle Architecture Change-2
Time Frame: Before, at the end of the fourth week and the eighth week
Pennation angle of the vastus lateralis and biceps femoris longus muscles
Before, at the end of the fourth week and the eighth week
Muscle Architecture Change-3
Time Frame: Before, at the end of the fourth week and the eighth week
Muscle thickness of the vastus lateralis and biceps femoris longus muscles
Before, at the end of the fourth week and the eighth week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Functional Performance Change-1
Time Frame: Before, at the end of the fourth week and the eighth week
Single leg jump distance
Before, at the end of the fourth week and the eighth week

Collaborators and Investigators

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

Investigators

  • Study Director: Ozlem Ulger, Hacettepe University

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)

November 21, 2022

Primary Completion (Anticipated)

March 15, 2023

Study Completion (Anticipated)

June 15, 2023

Study Registration Dates

First Submitted

September 23, 2022

First Submitted That Met QC Criteria

September 23, 2022

First Posted (Actual)

September 28, 2022

Study Record Updates

Last Update Posted (Actual)

November 29, 2022

Last Update Submitted That Met QC Criteria

November 22, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

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

product manufactured in and exported from the U.S.

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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