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Effect of Plyometric Exercise on Stability in Professional Indoor Soccer Players: A Pilot Study

Effect of Plyometric Exercise on Stability in Professional Indoor Soccer Players: A Pilot Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05760027
Acronym
PESF
Enrollment
10
Registered
2023-03-08
Start date
2023-03-14
Completion date
2023-07-31
Last updated
2023-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Plyometric Exercises

Brief summary

A program is proposed for two groups of professional indoor soccer players where the effect of plyometric exercises on body stability will be evaluated on a stabilometric platform.

Detailed description

A program is proposed for two groups of professional indoor soccer players where the effect of plyometric exercises on body stability will be evaluated on a stabilometric platform. Four evaluations will be carried out. An initial measurement before the beginning of the first intervention phase (Visit 1), after the intervention (Visit 2; day 30), after a 15-day washout period (Visit 3; day 45) and after the second intervention phase (Visit 4; day 75).

Interventions

OTHERPlyometric exercise

The group of athletes will perform plyometric stability exercises and their usual exercise for 30 days.

The group of athletes will perform their usual exercise for 30 days.

Sponsors

Universidad Católica San Antonio de Murcia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

The evaluator performing the measurements will be blinded.

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Professional soccer player in the first division of the National Soccer League (LNFS). * Age between 18 and 35 years old. * BMI between 18 and 32 Kg/m2.

Exclusion criteria

* Serious or terminal illness. * Participants with pain associated with chronic conditions. * Participants with body mass index above 32 kg/m2. * Inability to understand the informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Balance Phase 1Baseline and end of each intervention [Day 0 and day 30].Measurement of the balance measured as a percentage by pressure platform of professional indoor soccer players.
Balance Phase 2Baseline and end of each intervention [Day 45 and day 75].Measurement of the balance measured as a percentage by pressure platform of professional indoor soccer players.

Secondary

MeasureTime frameDescription
FlexibilityBaseline and end of each intervention [Day 0 and day 30].Flexibility will be measured with goniometer.
Number of injuriesBaseline and end of each intervention [Day 0 and day 30].The number of lesions will be collected during the course of the study.
Lower limb painBaseline and end of each intervention [Day 0 and day 30].Pain intensity will be measured with a Visual Analog Score (minimum value 0 - Maximum value 10). Higher values indicate a greater degree of pain
Anthropometric measurementsBaseline and end of each intervention [Day 0 and day 30].Anthropometric variables measured with a TANITA equipment.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026