Elastic Band Training Effects on Knee Strength and Performance in Female Football Players

January 23, 2025 updated by: Henrique Sousa

The Influence of Elastic Band Resistance Training on Knee Joint Muscle Strength and Performance-Related Parameters in Female Football Players: a Comparison of Three Development Phases

The goal of this clinical trial is to assess the effects of an 8-week strength training program with elastic bands on several physical components in female football players at the U15, U19, and Senior levels. The main question it aims to answer is:

Will a specific elastic band resistance training help improve some components of physical performance in female football players?

Participants will perform a bi-weekly elastic band resistance training program lasting 20 minutes per session over 8 weeks. This program will be incorporated into their in-season regimen, with assessments conducted in the week prior (week 0) and after the intervention (week 9).

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

This study will involve U15´, U19´ and adult female football (soccer) players doing a specific elastic band training plan over a period of 8 weeks. This plan will be done twice a week and will consist of 6 exercises, divided into two training sessions, each lasting approximately 20 minutes.

The week before the study begins (week 0), a demonstration will be given of the assessments and training plan that will be carried out during the following weeks, so that the participants have a better idea of what will happen. In addition, their height and weight will also have to be measured, followed by the first assessments. They will also fill in a questionnaire about their training habits and injury history.

They will then be randomized into two possible groups: the experimental group (EG) and the control group (CG). If the participant stays in the EG, she will have to do the above protocol and if she stays in the CG, she will only have to do the assessments, which will be done in the familiarization week (week 0) and the ninth week (week 9).

Study Type

Interventional

Enrollment (Estimated)

60

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

    • Porto
      • Maia, Porto, Portugal, 4475-690, Maia
        • Recruiting
        • University of Maia
        • Contact:

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • belong to the U-15, U-19 or Senior level of a women's football (soccer) club;
  • be apart of a football championship (district or national)

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental: Elastic Band Group
Athletes that will participate in a bi-weekly elastic band resistance training program.
Elastic Band Resistance Training
No Intervention: Control: Standard Group
Athletes that will continue doing their standard training regiment.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Knee extension and flexion isometric strength
Time Frame: The evaluations will be conducted in the week prior (week 0) and after the intervention (week 9).
Maximal isometric knee extension and flexion force will be measured using a handheld dynamometer (DynaMo Plus, VALD Performance, Brisbane, Queensland, Australia). For the knee extension assessment, participants will be in a seated position, whereas during the knee flexion evaluation, the participants will be in a prone position. To generate their maximal torque, the dynamometer chain length will be adjusted so that their knee angle will be at ∼60° and ∼30°, for the knee extension and flexion, respectively. Participants will then apply a maximal isometric effort, maintaining it for 5s, without any subsidiary body movements.
The evaluations will be conducted in the week prior (week 0) and after the intervention (week 9).
Vertical jump
Time Frame: The evaluations will be conducted in the week prior (week 0) and after the intervention (week 9).
Jump height will be evaluated using force plates (ForceDecks, Vald). The players will perform the countermovement jump, where they will begin from an upright position; a rapid downward movement to a knee angle of ∼90°, immediately transitioning to propel themselves upwards into the air.
The evaluations will be conducted in the week prior (week 0) and after the intervention (week 9).
Change of direction sprint
Time Frame: The evaluations will be conducted in the week prior (week 0) and after the intervention (week 9).
The Modified T-Test will be implemented to assess change of direction sprint. This evaluation has within itself directional changes such as forward sprinting, left and right-side shuffling, and backpedaling. Photocells (WhittyGate, Microgate, Bolzano, Italy) will be used for a more precise time count.
The evaluations will be conducted in the week prior (week 0) and after the intervention (week 9).

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 (Estimated)

January 29, 2025

Primary Completion (Estimated)

April 11, 2025

Study Completion (Estimated)

April 28, 2025

Study Registration Dates

First Submitted

January 18, 2025

First Submitted That Met QC Criteria

January 23, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 23, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • EBT_HS_02

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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