Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07442305

Assessing Dietary Intake of Selected Food Components Using Short Questionnaires

The aim of the study is to validate short questionnaires for assessing dietary intake of selected food components, with a focus on dietary fibre and iron. Two internationally developed short questionnaires (FiberScreen [for dietary fibre] and IRONQ-FFQ [for iron]) were adapted to the Slovenian context and will be compared with the standard 24-hour dietary recall method.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

About this study

Based on previous research conducted in Slovenia and across Europe, it can be concluded that notable proportion of the Slovenian population does not meet the recommended intake of dietary fibre. At the same time, there are important population groups at increased risk of inadequate iron intake, particularly women of reproductive age. Both nutrients have significant implications for health and represent an important public health challenge that requires appropriate monitoring of dietary intake at the population level.

With the aim of providing a simple and reliable assessment of dietary fibre and iron intake in research, clinical, and public health settings, two short questionnaires adapted to the Slovenian context have been developed. The questionnaire for assessing dietary fibre intake (KV-PV) is based on the FiberScreen questionnaire developed by Dutch researchers and was adapted to the Slovenian dietary pattern using data from the SI.Menu study. The questionnaire for assessing iron intake (KV-Fe) is based on the validated IRONQ-FFQ and adapted for the Slovenian population.

Despite the content adaptation of both questionnaires to the Slovenian context, further validation is required before their practical application, in order to assess the reliability and usability of these tools for evaluating dietary fibre and iron intake in Slovenia.

The objectives of the project are to:

Determine dietary fibre intake as assessed by the KV-PV questionnaire. Determine iron intake as assessed by the KV-Fe questionnaire. Determine dietary fibre intake using a 5-day dietary record. Determine iron intake using a 5-day dietary record. Compare dietary fibre intake assessed by the KV-PV questionnaire with the 5-day dietary record and evaluate the reliability of the KV-PV.

Compare iron intake assessed by the KV-Fe questionnaire with the 5-day dietary record and evaluate the reliability of the KV-Fe.

Compare the results of two KV-PV questionnaires completed with a 6-week interval.

Compare the results of two KV-Fe questionnaires completed with a 6-week interval.

Examine potential correlations between the results of the tested questionnaires and selected biochemical indicators in participants who voluntarily opt for blood sampling.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Willingness to participate in the study.
  • Signed Statement of Informed and Voluntary Consent to Participate in the Study.
  • Age between 18 and 65 years at the time of enrolment in the study.
  • Willingness to comply with all study procedures and to keep a dietary record in accordance with the provided instructions.

Exclusion criteria

  • Pregnancy or breastfeeding.
  • Specific dietary practices followed by a small proportion of the population (veganism, LCHF, calorie-restricted diets; note: vegetarians are not excluded).
  • Diets prescribed by medical professionals.
  • Mental incapacity that prevents adequate understanding or participation.

Reasons for excluding a participant during the study:

  • Inability to participate in the study
  • Wishes to discontinue participation
  • Incomplete data provided

Treatment and study plan

5d-PD: Nutritional intakes using 24-h food recalls

Diagnostic Test

Assessment of food intake (5x 24-h dietary recalls) and estimation of nutritional intakes

KV-PV: Dietary fibre intake

Diagnostic Test

Dietary fibe intake assessed using KV-PV (Short questionnaire for the assessment of dietary fibre intake)

KV-Fe: Iron intake

Diagnostic Test

Iron intake using KV-Fe (Short questionnaire for the assessment of iron intake)

screening questionnaire

Diagnostic Test

Screening questionnaire: assessment of socio-demographic parameters, use of food supplements, health status, dietary habits

Blood biomarkets

Diagnostic Test

Subjects we be provided with option for laboratory assessment of iron status (ferritin, serum iron, and hemoglobin) and a basic lipid profile (total cholesterol, HDL cholesterol, LDL cholesterol, and triglycerides).

Primary outcomes

  1. Nutritional intake using 24-h food recalls (5d-PD)

    Time frame: 1 week

    Nutritional intake will be estimated using 24-h food recalls for 5 days (5d-PD)

  2. Dietary fibre intake (KV-PV)

    Time frame: 6 weeks

    Dietary fibe intake will be assessed using KV-PV (Short questionnaire for the assessment of dietary fibre intake) in beginning of the study and after about 6 weeks.

  3. Iron intake (KV-Fe)

    Time frame: 6 weeks

    Iron intake will be assesed using KV-Fe (Short questionnaire for the assessment of iron intake) n beginning of the study and after about 6 weeks.

Other outcomes

  1. Laboratory assessment of iron status: S-ferritin

    Time frame: once during 6 weeks of the study

    Laboratory assessment of iron status using blood analyses

  2. Laboratory assessment of iron status: S-iron

    Time frame: once during 6 weeks of the study

    Laboratory assessment of iron status using blood analyses

  3. Laboratory assessment of iron status: hemoglobin

    Time frame: once during 6 weeks of the study

    Laboratory assessment of iron status using blood analyses

  4. Laboratory assessment of blood lipids: total cholesterol

    Time frame: once during 6 weeks of the study

    laboratory assessment of lipid profile using blood analyses

  5. Laboratory assessment of blood lipids: HDL cholesterol

    Time frame: once during 6 weeks of the study

    laboratory assessment of lipid profile using blood analyses

  6. Laboratory assessment of blood lipids: LDL cholesterol

    Time frame: once during 6 weeks of the study

    laboratory assessment of lipid profile using blood analyses

  7. Laboratory assessment of blood lipids: triglycerides

    Time frame: once during 6 weeks of the study

    laboratory assessment of lipid profile using blood analyses

Study contacts

Contact information is provided by the study sponsor or research team.

Liza Mohoric

CONTACT

Maša Hribar, PhD

CONTACT

[email protected]

+386 590 68870

Sponsors and collaborators

Lead sponsor

Institute of Nutrition, Slovenia (Nutris)

Other

Registry information

Official study title

Validation of Short Questionnaires for Assessing Dietary Intake of Selected Food Components

Acronym: NutriPlant/FFQ

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Mar 2, 2026
Registry last updated
Mar 2, 2026

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.