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

Study Locations

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.

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

Keywords

Other Study ID Numbers

  • 27-11-24

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.

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