Skip to main content
OpenTrials
Completed

NCT Number: NCT06536270

Development of a Web-Based Food Frequency Questionnaire and Diet Quality Score for Turkish Adults

This research aims to adapt and validate the web-based eNutri Food Frequency Questionnaire (FFQ) and Diet Quality Score (DQS) for the Turkish population, addressing the current gap in dietary assessment tools for Turkey. The study involves adapting the UK-based eNutri FFQ to reflect Turkish dietary habits, including revising the food list, capturing portion size photos, and incorporating local food composition data. The revised FFQ will be validated against three 24-hour dietary recalls and tested for reproducibility.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Istanbul Medipol University

Istanbul, Beykoz, 34810, Turkey (Türkiye)

About this study

Background: Non-communicable diseases (NCDs), such as cardiovascular diseases, are important global health concerns. Accurate dietary assessment is pivotal in understanding the relationship between food intake and health outcomes. Presently, there is a notable absence of a comprehensive dietary assessment tool tailored for the Turkish population.

Objective: The primary objective of this research is to adapt and validate the web-based eNutri Food Frequency Questionnaire (FFQ) and Diet Quality Score (DQS) for the Turkish population, addressing the current gap in dietary assessment methods.

Design and Proposed Analysis: The first part of the study will involve adapting the UK-based e-Nutri FFQ to reflect dietary habits of Turkish adults (eNutri-Turkey), such as revising the food list, taking portion size photos, and incorporating Turkish food composition data. The revised FFQ delivered online will be validated against three 24-hour recalls by phone (reference method) and the FFQ will be administered twice to assess reproducibility. The study will employ Cronbach's Alpha for internal consistency and the Bland-Altman method for validity. Additionally, inter-rater reliability and reproducibility will be assessed through Cohen's Kappa and ICC analysis, respectively. The eNutri DQS will be adapted in accordance with Turkish dietary guidelines. Following the adaptation, its validity will be assessed using existing Turkish population nutrient data. This analysis will involve retrospectively calculating the DQS and examining its associations with key risk markers of chronic diseases (BMI, blood pressure, blood glucose and cholesterol levels). Additionally, two qualitative studies will be conducted before starting the validation study. Dietitians and nutrition academics from Turkey (n=10) will provide insights on the suitability and effectiveness of eNutri-Turkey through one-to-one interviews. Feedback received will be used to improve the FFQ and DQS.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 18-65 years.
  • No diagnosed medical conditions (e.g., diabetes, heart disease, cancer, gastrointestinal conditions).
  • Not pregnant or lactating.
  • No food allergies or intolerances.
  • Not following a specialized diet (e.g., vegan, weight-loss, sports nutrition regimen; vegetarians are eligible).
  • Not receiving face-to-face nutritional services or dietary advice from a medical professional.
  • Not participating in another nutrition study.
  • Residing in Turkey.

Exclusion criteria

  • Individuals with any diagnosed medical conditions.
  • Pregnant or lactating women.
  • Individuals with food allergies or intolerances.
  • Those following a specialized diet (except vegetarians).
  • Participants currently receiving face-to-face nutritional services or dietary advice.
  • Individuals involved in another nutrition study.
  • Individuals residing outside of Turkey.

Treatment and study plan

A validation and reproducibility study with a cross-sectional component

Other

The primary intervention in this study involves adapting and validating the eNutri web-based Food Frequency Questionnaire and Diet Quality Score for the Turkish population.

Primary outcomes

  1. Validity of the web-based FFQ

    Time frame: 14-day period

    Assesses the validity of the adapted eNutri FFQ by comparing its results with those from three 24-hour dietary recalls. Validity is evaluated based on nutrient intake measurements.

  2. Reproducibility of the web-based FFQ

    Time frame: 14-day period

    Measures reproducibility by administering the FFQ twice to participants and analyzing the consistency of the results. Consistency of results; statistical measures will be used for analysis.

Secondary outcomes

  1. Usability of the web-based FFQ

    Time frame: Immediately after the first FFQ administration

    Evaluates usability through participant feedback on a scale (e.g., Likert scale) on the clarity and ease of use of the FFQ and portion size images.

  2. Usability Comparison of 24-Hour Recall and web-based FFQ

    Time frame: Immediately after the second FFQ administration

    Compares dietary intake data obtained from the 24-hour recall method (reference method) with that obtained from the FFQ administered after the second FFQ to assess usability.

Sponsors and collaborators

Lead sponsor

Medipol University

Other

Collaborators

  • University of Reading

Registry information

Official study title

Development of a Web-Based Food Frequency Questionnaire and Diet Quality Score for Turkish Adults: Validity and Reliability

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Aug 2, 2024
Registry last updated
Jan 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.