Plyometric ExercisesPESFNCT05760027
Effect of Plyometric Exercise on Stability in Professional Indoor Soccer Players: A Pilot Study
A study testing Plyometric exercise and Regular exercise in people with Plyometric Exercises, run by Universidad Católica San Antonio de Murcia at 1 site in Spain.
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 35 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Plyometric Exercises
- What is being tested?
- Plyometric exercise and Regular exercise
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 10 participants
- Where
- 1 siteSpain
- Study dates
- 14 Mar 2023to Jul 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 35 years
- Men only
- Healthy volunteers accepted
- Adult
Who may be able to join
- 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.
Who cannot join
- 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.
Trial locations and contacts
1 site in 1 country.
About this study
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.
Read the 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).
- Conditions
- Plyometric Exercises
- Being tested
- Plyometric exercise, Regular exercise
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Plyometric exerciseOther
The group of athletes will perform plyometric stability exercises and their usual exercise for 30 days.
Regular exerciseOther
The group of athletes will perform their usual exercise for 30 days.
| Study group | Role | What they receive |
|---|---|---|
| Plyometric exercise | Experimental | The group of athletes will perform plyometric stability exercises and their usual exercise for 30 days. Receives: Other: Plyometric exercise |
| Regular exercise | Other | The group of athletes will their usual exercise for 30 days. Receives: Other: Regular exercise |
What is being measured
The primary outcome is the main question the study is designed to answer.
Balance Phase 1
Measurement of the balance measured as a percentage by pressure platform of professional indoor soccer players.
Measured: 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.
Measured: Baseline and end of each intervention [Day 45 and day 75].
Secondary outcomes (10)
Flexibility
Flexibility will be measured with goniometer.
Measured: Baseline and end of each intervention [Day 0 and day 30].
Flexibility
Flexibility will be measured with goniometer.
Measured: Baseline and end of each intervention [Day 45 and day 75].
Flexibility
Flexibility will be measured with Lunge test.
Measured: Baseline and end of each intervention [Day 0 and day 30].
Flexibility
Flexibility will be measured with Lunge test.
Measured: Baseline and end of each intervention [Day 45 and day 75].
Number of injuries
The number of lesions will be collected during the course of the study.
Measured: Baseline and end of each intervention [Day 0 and day 30].
Number of injuries
The number of lesions will be collected during the course of the study.
Measured: Baseline and end of each intervention [Day 45 and day 75].
Lower limb pain
Pain intensity will be measured with a Visual Analog Score (minimum value 0 - Maximum value 10). Higher values indicate a greater degree of pain
Measured: Baseline and end of each intervention [Day 0 and day 30].
Lower limb pain
Pain intensity will be measured with a Visual Analog Score (minimum value 0 - Maximum value 10). Higher values indicate a greater degree of pain
Measured: Baseline and end of each intervention [Day 45 and day 75].
Anthropometric measurements
Anthropometric variables measured with a TANITA equipment.
Measured: Baseline and end of each intervention [Day 0 and day 30].
Anthropometric measurements
Anthropometric variables measured with a TANITA equipment.
Measured: Baseline and end of each intervention [Day 45 and day 75].
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Mar 2023
- Study start14 Mar 2023
- Primary completionApr 2023 (estimated)
- Study completionJul 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Plyometric ExercisesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 10 participants (actual)
Sponsor and investigators
- Lead sponsor
- Universidad Católica San Antonio de Murcia
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Inmaculada Ruiz Lopez, Universidad Católica San Antonio de Murcia
- Investigators
- Universidad Católica San Antonio de Murcia Universidad Católica San Antonio de Murcia, Principal investigator, Universidad Católica San Antonio de Murcia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05760027
- Sponsor's protocol ID
- UCAM CE012305
- Acronym
- PESF
- Status last verified
- Mar 2023
- First submitted
- 2 Feb 2023
- Last updated
- 30 Mar 2023
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 30 Mar 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of Plyometric Exercise on Stability in Professional Indoor Soccer Players: A Pilot Study
- ClinicalTrials.gov ID
- NCT05760027
- Acronym / sponsor ID
- PESF / UCAM CE012305
- Conditions
- Plyometric Exercises
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 10 participants (actual)
- Lead sponsor
- Universidad Católica San Antonio de MurciaUniversity, hospital or other
- Study start
- 14 Mar 2023 (actual)
- Primary completion
- Apr 2023 (estimated)
- Study completion
- Jul 2023 (estimated)
- First posted
- 8 Mar 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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).
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Plyometric exercise | Experimental | Other: Plyometric exerciseThe group of athletes will perform plyometric stability exercises and their usual exercise for 30 days. |
| Regular exercise | Other | Other: Regular exerciseThe group of athletes will their usual exercise for 30 days. |
Who may qualify
- Ages
- 18 to 35 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- 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.
Key exclusion criteria (4 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Plyometric exerciseThe group of athletes will perform plyometric stability exercises and their usual exercise for 30 days. | Other | Plyometric exercise |
| Regular exerciseThe group of athletes will perform their usual exercise for 30 days. | Other | Regular exercise |
Primary outcome
Balance Phase 1
Time frame: Baseline 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 2
Time frame: Baseline 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.
10 secondary outcomes
Flexibility
Time frame: Baseline and end of each intervention [Day 0 and day 30].
Flexibility
Time frame: Baseline and end of each intervention [Day 45 and day 75].
Flexibility
Time frame: Baseline and end of each intervention [Day 0 and day 30].
Flexibility
Time frame: Baseline and end of each intervention [Day 45 and day 75].
Number of injuries
Time frame: Baseline and end of each intervention [Day 0 and day 30].
Number of injuries
Time frame: Baseline and end of each intervention [Day 45 and day 75].
Lower limb pain
Time frame: Baseline and end of each intervention [Day 0 and day 30].
Lower limb pain
Time frame: Baseline and end of each intervention [Day 45 and day 75].
Anthropometric measurements
Time frame: Baseline and end of each intervention [Day 0 and day 30].
Anthropometric measurements
Time frame: Baseline and end of each intervention [Day 45 and day 75].
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 30 Mar 2023.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Universidad Católica San Antonio de Murcia Universidad Católica San Antonio de Murcia principal investigator
Universidad Católica San Antonio de Murcia
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Plyometric exercise and Regular exercise in people with Plyometric Exercises, run by Universidad Católica San Antonio de Murcia at 1 site in Spain.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 30 Mar 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Balance Phase 1 (time frame: Baseline and end of each intervention [Day 0 and day 30].). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Mar 2023.