- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05558033
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
Intervention / Treatment
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
- Name: Murat Emirzeoğlu, MSc
- Phone Number: +90 312 305 15 77
- Email: muratemirzeoglu@gmail.com
Study Locations
-
-
-
Trabzon, Turkey
- Recruiting
- Of Football Club
-
Contact:
- Murat Emirzeoğlu
- Phone Number: +90 462377 8842
- Email: muratemirzeoglu@gmail.com
-
-
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.
Sponsor
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
Keywords
Other Study ID Numbers
- 2022-11475
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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