NCT06800079

Brief Summary

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).

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 18, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

January 29, 2025

Completed
Same day until next milestone

Study Start

First participant enrolled

January 29, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 11, 2025

Completed
17 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 28, 2025

Completed
Last Updated

January 29, 2025

Status Verified

January 1, 2025

Enrollment Period

2 months

First QC Date

January 18, 2025

Last Update Submit

January 23, 2025

Conditions

Keywords

Elastic BandsResistance TrainingWomenFootballPerformance

Outcome Measures

Primary Outcomes (3)

  • Knee extension and flexion isometric strength

    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

    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

    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).

Study Arms (2)

Experimental: Elastic Band Group

EXPERIMENTAL

Athletes that will participate in a bi-weekly elastic band resistance training program.

Other: EBT

Control: Standard Group

NO INTERVENTION

Athletes that will continue doing their standard training regiment.

Interventions

EBTOTHER

Elastic Band Resistance Training

Experimental: Elastic Band Group

Eligibility Criteria

Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • 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)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Maia

Maia, Porto District, 4475-690, Maia, Portugal

RECRUITING

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Henrique Sousa, MsC.

Study Record Dates

First Submitted

January 18, 2025

First Posted

January 29, 2025

Study Start

January 29, 2025

Primary Completion

April 11, 2025

Study Completion

April 28, 2025

Last Updated

January 29, 2025

Record last verified: 2025-01

Locations