- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07408739
Association Between Weekly Strength Training Load and Perceived Physical Performance in Non-Professional Soccer Players
Association Between Weekly Strength Training Load and Perceived Physical Performance in Non-Professional Soccer Players: A Cross-Sectional Observational Study
Background. Strength training is a key component of physical performance in soccer. However, in non-professional players, evidence regarding the relationship between weekly strength training load and perceived physical performance remains limited, particularly when considering factors such as fatigue, pain, and motivation.
Objective. To analyze the association between self-reported weekly strength training load and perceived physical performance in non-professional soccer players, and to examine the influence of perceived fatigue, musculoskeletal pain, and exercise motivation on this relationship.
Methods. An observational, analytical, cross-sectional study conducted using a structured, self-administered online questionnaire. The dependent variable will be perceived physical performance, assessed using the Perceived Performance in Sports Questionnaire. Independent variables will include weekly strength training load, measured using the session Rating of Perceived Exertion (sRPE), perceived fatigue assessed with the Fatigue Severity Scale, and motivation toward training and sport participation assessed with the Behavioral Regulation in Exercise Questionnaire-2. Adjustment variables will include age, sex, playing position, competitive level, sporting experience, mean match playing time (minutes per match), body mass index, and overall weekly training load. Descriptive analyses and multivariable regression models will be performed.
Expected results. To identify the relationship between weekly strength training load and perceived physical performance, and to determine the physical and psychosocial factors associated with lower self-perceived performance in non-professional soccer players.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
Principality of Asturias
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Oviedo, Principality of Asturias, Spain, 33006
- Universidad de Oviedo
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Age between 18 and 40 years.
- Competing in the 3ª RFEF category.
- Male sex.
- Having at least two years of seniority in federated football.
- Signing the informed consent document.
Exclusion Criteria:
- Athletes with injuries lasting more than 3 months during the last season.
- Participation in fewer than two weekly group training sessions (one or none).
- Having undergone lower-limb surgery in the last 24 months.
- Players who, despite being able to attend training sessions on a continuous basis, have a regular occupational activity that causes such a high physical workload that their sports performance is limited in training and/or competition.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Observational group
Non-professional soccer players
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Active non-professional (amateur) soccer players.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measurement of perceived physical performance
Time Frame: Screening visit
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This variable will be assessed using the Spanish version of the Perceived Performance in Sports Questionnaire.
This instrument measures athletes' subjective evaluation of their own performance during competition or sport practice.
It consists of five items rated on a 1-5 Likert scale, with the final score calculated as the mean of the items; higher scores indicate better perceived performance.
As no specific cut-off points are established, the score will be interpreted as a continuous variable.
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Screening visit
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measurement of weekly strength training load
Time Frame: Screening visit
|
Weekly strength training load will be quantified using the session Rating of Perceived Exertion (sRPE; Borg CR-10).
Participants will report session duration and perceived intensity (0-10) for all strength sessions in the previous week.
Weekly load will be calculated as the sum of sRPE × duration (minutes) across sessions.
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Screening visit
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Measurement of perceived fatigue
Time Frame: Screening visit
|
This variable will be assessed using the Spanish version of the Fatigue Severity Scale (FSS).
This self-reported questionnaire evaluates the impact of fatigue on daily functioning and consists of nine items rated on a 1-7 Likert scale.
The final score is calculated as the mean of the items, with higher values indicating greater perceived fatigue; a mean score ≥4 is considered indicative of clinically significant fatigue.
|
Screening visit
|
|
Measurement of motivation toward training and sport participation
Time Frame: Screening visit
|
This variable will be assessed using the Spanish version of the Behavioral Regulation in Exercise Questionnaire-2 (BREQ-2).
This self-reported instrument, grounded in Self-Determination Theory, evaluates different types of motivational regulation toward exercise.
It consists of 19 items distributed across the dimensions of amotivation, external regulation, introjected regulation, identified regulation, and intrinsic motivation.
Higher scores in autonomous regulation, particularly intrinsic motivation, are associated with greater adherence to and engagement in sport practice.
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Screening visit
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Measurement of age
Time Frame: Screening visit
|
This confounding or moderating variable, used to control for individual characteristics, will be measured in years.
|
Screening visit
|
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Measurement of gender
Time Frame: Screening visit
|
This confounding or moderating variable, used to control for individual characteristics, will be recorded as a dichotomous variable (male/female).
|
Screening visit
|
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Measurement of playing position
Time Frame: Screening visit
|
This confounding or moderating variable, used to control for individual characteristics, will be recorded as an ordinal variable (goalkeeper / defender / midfielder / forward).
|
Screening visit
|
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Measurement of competitive category
Time Frame: Screening visit
|
This confounding or moderating variable, used to control for individual characteristics, will be recorded as an ordinal variable (e.g., first regional division / second regional division, etc.).
|
Screening visit
|
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Measurement of soccer-specific experience
Time Frame: Screening visit
|
This confounding or moderating variable, used to control for individual characteristics, will be measured as a continuous variable, defined as the number of competitive seasons played.
|
Screening visit
|
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Measurement of average match playing time
Time Frame: Screening visit
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This confounding or moderating variable, used to control for individual characteristics, will be recorded as an ordinal variable (<45 minutes / 45-90 minutes / >90 minutes).
|
Screening visit
|
|
Measurement of body mass index
Time Frame: Screening visit
|
This confounding or moderating variable, used to control for individual characteristics, will be calculated from body mass and height (kg/m²).
|
Screening visit
|
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Measurement of overall weekly training load
Time Frame: Screening visit
|
This confounding or moderating variable, used to control for individual characteristics, will be assessed as the mean perceived exertion of all training sessions (strength training plus field-based sessions) using a 0-10 rating of perceived exertion scale.
|
Screening visit
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Estimated)
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
Other Study ID Numbers
- FutRend
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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