NCT05760027

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.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
10

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 2, 2023

Completed
1 month until next milestone

First Posted

Study publicly available on registry

March 8, 2023

Completed
6 days until next milestone

Study Start

First participant enrolled

March 14, 2023

Completed
18 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2023

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2023

Completed
Last Updated

March 30, 2023

Status Verified

March 1, 2023

Enrollment Period

18 days

First QC Date

February 2, 2023

Last Update Submit

March 29, 2023

Conditions

Outcome Measures

Primary Outcomes (2)

  • Balance Phase 1

    Measurement of the balance measured as a percentage by pressure platform of professional indoor soccer players.

    Baseline and end of each intervention [Day 0 and day 30].

  • Balance Phase 2

    Measurement of the balance measured as a percentage by pressure platform of professional indoor soccer players.

    Baseline and end of each intervention [Day 45 and day 75].

Secondary Outcomes (10)

  • Flexibility

    Baseline and end of each intervention [Day 0 and day 30].

  • Flexibility

    Baseline and end of each intervention [Day 45 and day 75].

  • Flexibility

    Baseline and end of each intervention [Day 0 and day 30].

  • Flexibility

    Baseline and end of each intervention [Day 45 and day 75].

  • Number of injuries

    Baseline and end of each intervention [Day 0 and day 30].

  • +5 more secondary outcomes

Study Arms (2)

Plyometric exercise

EXPERIMENTAL

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

Other: Plyometric exercise

Regular exercise

OTHER

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

Other: Regular exercise

Interventions

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

Plyometric exercise

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

Regular exercise

Eligibility Criteria

Age18 Years - 35 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Universidad Católica San Antonio de Murcia

Murcia, 30107, Spain

Location

MeSH Terms

Interventions

Plyometric Exercise

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesPhysical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Universidad Católica San Antonio de Murcia Universidad Católica San Antonio de Murcia

    Universidad Católica San Antonio de Murcia

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
The evaluator performing the measurements will be blinded.
Purpose
PREVENTION
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

February 2, 2023

First Posted

March 8, 2023

Study Start

March 14, 2023

Primary Completion

April 1, 2023

Study Completion

July 1, 2023

Last Updated

March 30, 2023

Record last verified: 2023-03

Locations