CClinicalTrials.gg
RecruitingNCT06648616Updated Oct 18, 2024

Impact of Elastic Band Resistance Training on Female Football Performance: A Pilot Study

An interventional study of EBT in Physical Perfrormance Parameters, sponsored by University Institute of Maia. Recruiting at 1 site in Portugal. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-10-18.

Sponsored by University Institute of Maia · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 10 months ago, but the record still lists the study as recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
10
Allocation
Not applicable
Ages
18 Years and older
Sex
Female
01

Study summary

The goal of this clinical trial is to assess the effects of a 6-week strength training program with elastic bands on several physical components in adult female football players. The main question it aims to answer is:

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

Participants will perform a bi-weekly elastic band resistance training, during a period of 6-weeks. This program will be incorporated into their in-season regimen, before their training session.

02

Conditions studied

  • Physical Perfrormance Parameters
03

In context

Lead sponsor

University Institute of Maia is the lead sponsor of 12 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:

  • be over 18 years of age;
  • belong in the senior level of an amateur or professional women´s football club;
  • play in one of the three Portuguese national women´s football leagues.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
10 participants (estimated)

Study arms

  • Experimental
    Elastic Band Group

    Athletes that have participated in a bi-weekly elastic band resistance training program.

    Other: EBT

Interventions

  • OtherEBT

    Elastic Band Resistance Training

06

What researchers measure

Primary outcomes

  1. 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.

    Time frame: At the beginning and end of the study (Week 1 and Week 6)

  2. Vertical jump

    Jump height was evaluated using an optical measurement system (OptoJump, Microgate, Bolzano, Italy). 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.

    Time frame: At the beginning and end of the study (Week 1 and Week 6)

  3. 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.

    Time frame: At the beginning and end of the study (Week 1 and Week 6)

07

Study locations

1 of 1 sites recruiting
  • University of Maia
    Maia, Porto 4475-690 Maia, Portugal
    • Henrique Sousa, MSc · Contact · +351934551303
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 18, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06648616
Lead sponsor
University Institute of Maia
Responsible party
Henrique Sousa (Principal Investigator, University of Maia) — Principal investigator
First posted
Oct 18, 2024
Start date
Oct 2024 (estimated)
Primary completion
Dec 2024 (estimated)
Completion
Jan 2025 (estimated)
Last update
Oct 18, 2024

Study contacts

Henrique Sousa, MSc
Contact
hsousa.dcd@umaia.pt
+351934551303

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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