- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07488000
Plyometric Exercises During the Winter Pre-season in Sprinters
Association Between a Winter Pre-season Plyometric Exercise Programme and Performance and Health-related Outcomes in Sprinters: a Prospective Cohort Study
Background. Plyometric training is an effective strategy to improve power and performance in sprint-based sports; however, evidence regarding its actual effects in athletes during the winter season and its potential influence on the occurrence of health problems remains limited.
Objective. To analyse the association between participation in a plyometric exercise programme during the winter pre-season and competitive performance, as well as the occurrence of lower-limb health problems in sprinters.
Methods. This will be a prospective observational cohort study with fully online data collection. Federated sprinters or athletes affiliated with athletics clubs will be included. The main exposure will be participation in a plyometric exercise programme (≥2 sessions per week in January). Outcomes will be winter competitive performance (best official time) and lower-limb health problems assessed using the OSTRC-H2 questionnaire. Control variables will include sleep quality (PSQI), internal training load (session-RPE), injury history, and competitive level. Statistical analyses will include linear and logistic regression models adjusted for potential confounders.
Expected results. A positive association is expected between engagement in plyometric training and competitive performance, along with a lower frequency of lower-limb health problems, particularly among athletes with adequate sleep quality and a well-balanced training load.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Principality of Asturias
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Murcia, Principality of Asturias, Spain, 33006
- Universidad Católica San Antonio de Murcia
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age ≥16 years
- Regular participation in sprint events (60-400 m)
- Planned participation in winter competitions
- Membership of an athletics club
- Provision of digital informed consent
Exclusion Criteria:
- Recent acute lower-limb injury preventing training
- Medical contraindication to plyometric training
- Inability to complete follow-up
- Low questionnaire completion rate (<70%).
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Observational group with intervention
Athletes undertaking plyometric training
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Participation in a structured plyometric exercise programme during the winter pre-season (≥2 sessions per week)
|
|
Observational group without intervention
Athletes not undertaking plyometric training
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Winter pre-season training programme without plyometric exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of changes in winter competitive performance at baseline, after the winter pre-season, and after the competitive season
Time Frame: Baseline, through study completion, an average of 1 month
|
Winter competitive performance will be measured using the best official time recorded by each athlete in their main event (60, 100, 200, or 400 metres) during the winter season.
The value will be expressed in seconds and will be obtained via self-report in the final questionnaire, together with the competition in which it was achieved.
This continuous variable will represent the primary performance outcome.
|
Baseline, through study completion, an average of 1 month
|
|
Assessment of changes in the occurrence of lower-limb health problems at baseline, after the winter pre-season, and after the competitive season
Time Frame: Baseline, through study completion, an average of 1 month
|
The occurrence of lower-limb health problems will be assessed using the Oslo Sports Trauma Research Center Overuse Injury Questionnaire (OSTRC-O), Spanish validated version.
Based on the weekly reports, two indicators will be derived: the presence of at least one substantial lower-limb health problem (dichotomous variable: yes/no) and the total number of weeks with any health problem in this location (discrete variable).
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Baseline, through study completion, an average of 1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of changes in sleep quality at baseline, after the winter pre-season, and after the competitive season
Time Frame: Baseline, through study completion, an average of 1 month
|
Sleep quality will be assessed using the Spanish version of the Pittsburgh Sleep Quality Index (PSQI).
This scale yields a global score ranging from 0 to 21, with higher scores indicating poorer sleep quality.
It will be administered at baseline and at the end of the season
|
Baseline, through study completion, an average of 1 month
|
|
Assessment of changes in the internal training load at baseline, after the winter pre-season, and after the competitive season
Time Frame: Baseline, through study completion, an average of 1 month
|
Internal training load will be calculated using the session-RPE method (14).
This assessment is based on weekly training duration in minutes multiplied by the global perceived exertion rated on the Borg CR10 scale.
From the weekly records, the mean weekly training load will be derived as a continuous variable.
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Baseline, through study completion, an average of 1 month
|
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Assessment of the previous performance at baseline
Time Frame: Baseline
|
Previous performance will be defined as the best official time recorded during the previous season, expressed in seconds, and will be used as a covariate to adjust for baseline performance level.
|
Baseline
|
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Assessment of lower-limb injury history at baseline
Time Frame: Baseline
|
Lower-limb injury history over the previous 12 months will be recorded as a dichotomous variable (yes/no), with documentation of the primary injury location.
|
Baseline
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of main sprint event at baseline
Time Frame: Baseline
|
Each athlete's main sprint event (60, 100, 200, or 400 metres) will be recorded.
This variable will be used as an indicator of sporting context.
|
Baseline
|
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Assessment of the athlete's competitive level at baseline
Time Frame: Baseline
|
Competitive level will be recorded (regional or national).
This variable will be used as an indicator of sporting context.
|
Baseline
|
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Assessment of years of experience in sprint athletics at baseline
Time Frame: Baseline
|
The number of years of experience in sprinting (number of competitive seasons) will be recorded as a continuous variable.
|
Baseline
|
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Assessment of athletes' sex at baseline
Time Frame: Baseline
|
Sex (male/female) will be recorded as a basic demographic variable.
|
Baseline
|
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Assessment of athletes' age at baseline
Time Frame: Baseline
|
Age (continuous quantitative variable) will be recorded as a basic demographic variable.
|
Baseline
|
Collaborators and Investigators
Investigators
- Principal Investigator: Rubén Cuesta-Barriuso, PhD, Universidad de Oviedo
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Nervous System Diseases
- Mental Disorders
- Wounds and Injuries
- Sleep Wake Disorders
- Sleep Disorders, Intrinsic
- Dyssomnias
- Sleep Initiation and Maintenance Disorders
- Athletic Injuries
- Motor Activity
- Movement
- Musculoskeletal Physiological Phenomena
- Musculoskeletal and Neural Physiological Phenomena
- Therapeutics
- Physical Therapy Modalities
- Patient Care
- Exercise Therapy
- Rehabilitation
- Aftercare
- Continuity of Patient Care
- Physical Conditioning, Human
- Exercise
- Plyometric Exercise
Other Study ID Numbers
- VelPli
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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