- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06713954
Analysis of Dietary Intake in Professional Female Football Players
December 3, 2024 updated by: Blanca Roman-Viñas, MD, University Ramon Llull
Analysis of Dietary Intake in Professional Female Football Players: Variations According to Playing Position, Age, and Country
This study evaluates the dietary intake of professional female footballers against nutritional guidelines, analysing differences by age, position, and location (UK vs Spain).
Using a cross-sectional design, it will include 20-30 players per club from four clubs, aged 18+, collected via the Snap-N-Send method and analysed with Nutritics software.
Variables include energy intake, macronutrients, and micronutrients, with data assessed using MANOVA, t-tests, and Shapiro-Wilk tests.
The aim is to determine dietary adequacy and provide insights to improve nutrition education and wellbeing for female athletes.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
The aim of this research is to evaluate the dietary intake of female footballers against established nutritional guidelines, while analysing the variables of age, playing position and location to identify if there is a difference in intake across the groups.
The study will employ an observational, descriptive, and cross-sectional research design, focusing on female footballers from professional clubs, specifically two clubs in United Kingdom and two clubs in Spain.
There is an anticipated sample size of 20 to 30 participants from each club.
Inclusion criteria will be female participants who are professional footballers, aged 18 and older and free of disease.
Dependent variables from dietary intake will include energy intake (kcal), energy availability (kcal/kg fat free mass/day), protein (g/day), carbohydrates (g/day), fat (%), vitamin D (mg/day), calcium (mg/day) and iron (mg/day).
These will be collected using the scientifically valid Snap-N-Send method and analysed with Nutritics dietary analysis software, which has been validated for assessing macronutrients and micronutrients.
Independent variables will consist of age groups, playing positions, and country of origin (England or Spain).
Dietary intake will be recorded through WhatsApp, with subsequent data entry and storage in Nutritics.
Statistical analyses will include MANOVA, used to compare dietary data among groups, one-sample t-test to test against published recommendations and the Shapiro-Wilk test to assess normality in data distribution.
This study aims to assess the adequacy of the players' dietary intake in relation to established nutritional recommendations from different backgrounds and characteristics.
Furthermore, practitioners can potentially make informed decisions that improve the nutrition education given to female athletes, which contributes to their overall health and wellbeing.
Study Type
Observational
Enrollment (Estimated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Olivia C. Coope
- Phone Number: +34932533256
- Email: oliviacharlottec@blanquerna.url.edu+34932533256
Study Locations
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-
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Barcelona, Spain, 08010
- Recruiting
- Blanquerna Institute, Universitat Ramon Llull
-
Contact:
- Olivia C. Coope
- Phone Number: +34932533256
- Email: oliviacharlottec@blanquerna.url.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Age=
- 18-24 years of age
- 25-31 years of age
Playing position=
- Defenders: Centre-backs, fullbacks, wingbacks, goalkeepers
- Midfielders: Central midfielders, attacking midfielders, defensive midfielders
- Wingers: Left wingers and right wingers
- Forwards: Strikers and centre-forwards
Country=
- England
- Spain
Description
Inclusion Criteria:
- Female or assigned female at birth
- Playing football professionally
- At a sub-elite to elite standard
- Above the age of 18
- Healthy and free of disease
Exclusion Criteria:
- Active supplementation with ergogenic aids
- Active pregnancy
- No signing of the consent form
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Female footballers
Female footballers of varying ages, playing positions and countries
|
Dietary intake data will be collected using the Snap-N-Send method, a tool with enhanced validity for assessing athlete total energy intake, where participants will take photographs of their meals and share them via WhatsApp directly with the researcher.
Before the study commences, participants will receive standardised instructions on photographing food and adding details in the message such as title, portion sizes and ingredients alongside each photo to enhance data precision.
The principal investigator will input these photographs with the added information into Nutritics dietary analysis software, where food weights, portion sizes, and nutritional content will be estimated and calculated.
Nutritics will then calculate dependent variables and convert it into a food diary report, aggregating the three days of food diary into average intake.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Carbohydrates
Time Frame: From enrollment to the end of assessment of 3 days
|
Amount of carbohydrates in grams from an average of 3 days
|
From enrollment to the end of assessment of 3 days
|
|
Energy intake
Time Frame: From enrollment to the end of assessment of 3 days
|
Average of energy intake in calories over 3 days
|
From enrollment to the end of assessment of 3 days
|
|
Protein
Time Frame: From enrollment to the end of assessment of 3 days
|
Average of protein in grams over 3 days
|
From enrollment to the end of assessment of 3 days
|
|
Fat
Time Frame: From enrollment to the end of assessment of 3 days
|
Average of percentage of fat over 3 days
|
From enrollment to the end of assessment of 3 days
|
|
Energy availability
Time Frame: From enrollment to the end of assessment of 3 days
|
Energy availability will be calculated by estimating fat-free mass (FFM) through the Boer equation, which uses weight and height.
The formula for females is FFM (kg) = 0.252 × Weight (kg) + 0.473 × Height (cm) - 48.3.
Total energy intake (TEI) will be determined from average daily calorie intake.
Exercise energy expenditure (EEE) will be estimated based on activity duration and MET values using the Compendium of Physical Activities (Ainsworth et al., 2011).
The resulting EA will be calculated using the formula: EA = (TEI - EEE) / FFM.
The outcome will be an average of kcal/kg fat free mass/day over 3 days
|
From enrollment to the end of assessment of 3 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Calcium
Time Frame: From enrollment to the end of assessment of 3 days
|
Average of calcium intake in milligrams over 3 days
|
From enrollment to the end of assessment of 3 days
|
|
Iron
Time Frame: From enrollment to the end of assessment of 3 days
|
Average of iron intake in milligrams over 3 days
|
From enrollment to the end of assessment of 3 days
|
|
Vitamin D
Time Frame: From enrollment to the end of assessment of 3 days
|
Estimation of average of Vitamin D in micrograms over 3 days
|
From enrollment to the end of assessment of 3 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Blanca Roman Viñas, PhD, Universitat Ramon Llull
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 2, 2024
Primary Completion (Estimated)
February 1, 2025
Study Completion (Estimated)
March 1, 2025
Study Registration Dates
First Submitted
November 27, 2024
First Submitted That Met QC Criteria
November 27, 2024
First Posted (Actual)
December 3, 2024
Study Record Updates
Last Update Posted (Estimated)
December 6, 2024
Last Update Submitted That Met QC Criteria
December 3, 2024
Last Verified
December 1, 2024
More Information
Terms related to this study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.