Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06876272

Implementation and Evaluation of Nutrition Interventions

This project aims to implement and evaluate two multi-component dietary interventions focused on promoting healthy and sustainable eating behaviors and preventing weight gain among Flemish higher education students. These interventions will take place over a period of eight weeks and are specifically designed to support healthy lifestyle choices during the transition from secondary school to higher education, a critical period where unhealthy eating behaviors and weight gain are common.

The interventions will be conducted at a university and a college, utilizing nudges in student restaurants, social media campaigns via Instagram, and workshops to encourage healthy and sustainable eating habits. Effectiveness will be measured using questionnaires administered at three points in time: before the intervention (baseline), immediately after the intervention (post-intervention), and five months later (follow-up). Two other campuses will serve as a control group to compare results.

In addition to assessing effectiveness, a process evaluation will also be conducted. This will involve focus groups with students and stakeholders, as well as a process questionnaire, to gain insights into the implementation of the interventions and the experiences of those involved. If the interventions prove successful, they may be scaled up to other Flemish institutions as part of a broader strategy for cancer prevention.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–24 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Antwerp - Campus Drie Eiken, Antwerp, Antwerpen, Belgium

Loading trial locations.

About this study

As part of a Foundation against Cancer project in collaboration with the Consumer Behavior Research Group (Department of Marketing, Innovation, and Organization, Ghent University), the Research Group on Physical Activity and Nutrition for Health and Performance (MOVE) (Department of Movement and Sport Sciences, VUB), the Health Promotion Research Group (Department of Public Health and Primary Care, Ghent University), and the Flemish Institute for Healthy Living, we aim to encourage students to adopt healthier and more sustainable eating habits.

This project focuses on the implementation and evaluation of two multi-component dietary interventions to promote healthy eating behaviors and prevent weight gain among Flemish higher education students.

Since unhealthy eating habits and obesity are the two main risk factors for cancer, it is crucial to encourage young people to make healthy lifestyle choices. The transition from secondary school to higher education is a critical period for weight gain and the neglect of dietary guidelines, and students are often overlooked in health promotion initiatives.

The goal of this study is to implement and evaluate two dietary interventions developed within this project at two institutions (a university and a college). Over a period of eight weeks, various actions will take place, both online and on campus. For this study, the campus environment will be strategically adjusted using a range of nudges to promote healthy (and sustainable) eating behavior among students. These subtle modifications are designed to positively influence students' choices without limiting their autonomy. Examples include redesigning dining areas, placing healthy and sustainable options more prominently, and making healthier choices more visually appealing.

Additionally, targeted actions will raise students' awareness of healthy (and sustainable) eating behaviors. These include information campaigns on social media and organizing information stands on campus. These stands will provide students with accessible opportunities to obtain information, ask questions, and sample sustainable and healthy products. The combination of physical modifications and various activities will create an engaging learning environment that contributes to awareness and behavioral change in students' dietary habits.

Moreover, sales data from the student restaurant will be collected throughout the intervention period (from February to May 2025). By monitoring these figures, changes in students' purchasing behavior can be analyzed. This will provide insights into the impact of nudges and awareness campaigns on the sales of healthy and sustainable food options.

The effectiveness of the intervention will be assessed through questionnaires administered to students before, immediately after, and several weeks after the intervention to capture changes in eating behavior and associated determinants. Two other campuses will serve as control groups for comparison.

In addition, a comprehensive process evaluation will be conducted using a process questionnaire for students and focus groups with both students and stakeholders. This will provide insights into the implementation and experiences of the intervention.

If successful, the program can be scaled up to other Flemish higher education institutions as part of a broader cancer prevention strategy.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Higher education students:
  • Participant is willing and able to give informed consent for par-ticipation in the study;
  • Male, female or X, aged 18-24 years;
  • Healthy higher education students from institution X or campus Y.
  • Adopters and implementers:
  • Persons who are involved in the design, implementation, daily operations or management of the nutrition intervention.
  • Persons who have knowledge of the specific goals of the nutrition intervention.

Exclusion criteria

  • Higher education students:
  • Students who speak insufficient Dutch;
  • Students who are less than 18 years old.
  • Adopters and implementers:
  • Persons who speak insufficient Dutch.

Treatment and study plan

Healthy eating promoting programme

Behavioral

It is a comprehensive, multi-component intervention tailored specifically for higher education students. Unlike many traditional health programs, this intervention uniquely combines the use of social media campaigns, behavioral nudges in student cafeterias, and interactive boost workshops.

Primary outcomes

  1. Nutrition behaviour

    Time frame: 3 test occations: baseline, 10 weeks after baseline and 5 months after baseline.

    Measured using an online questionnaire specifically developed for this study. This section of the questionnaire incorporated a modified version of the Food Frequency Questionnaire (FFQ), adapted from the Health Behaviour in School-aged Children (HBSC) survey for high school students. The FFQ evaluates dietary intake by measuring the consumption of both healthy foods (e.g., vegetables, fruits) and unhealthy foods (e.g., sugary drinks, fast food). Responses were recorded on an ordinal frequency scale, ranging from "never" to "more than three times per day."

  2. Attitude

    Time frame: 3 test occations: baseline, 10 weeks after baseline and 5 months after baseline.

    Measured using an online questionnaire specifically developed for this study. This section incorporated adapted questions from the REWARD study, as well as the EAT 2 and EAT 3 surveys. Attitudes toward healthy eating were measured using a 5-point Likert scale, ranging from "strongly disagree" to "strongly agree."

  3. Nutrition knowledge

    Time frame: 3 test occations: baseline, 10 weeks after baseline and 5 months after baseline.

    Measured using an online questionnaire specifically developed for this study. This section incorporated questions from the General Nutrition Knowledge Questionnaire (GNKQ) and study-specific questions related to the intervention (e.g., daily water intake recommendations). Nutrition knowledge was evaluated through multiple-choice questions.

  4. Self-efficacy

    Time frame: 3 test occations: baseline, 10 weeks after baseline and 5 months after baseline.

    Measured using an online questionnaire specifically developed for this study. This section of the questionnaire incorporates adapted items from the REWARD study. Participants rated their confidence in making healthy and sustainable food choices using a 5-point Likert scale, ranging from "very difficult" to "very easy."

  5. Perceived food environment

    Time frame: 3 test occations: baseline, 10 weeks after baseline and 5 months after baseline.

    Measured using an online questionnaire specifically developed for this study. This section of the questionnaire incorporated questions adapted to students' contexts from the Perceived Food Environment Questionnaire. Responses were recorded on a 5-point Likert scale, ranging from "strongly disagree" to "strongly agree."

  6. Intention

    Time frame: 3 test occations: baseline, 10 weeks after baseline and 5 months after baseline.

    Measured using an online questionnaire specifically developed for this study. This section of the questionnaire incorporated a question derived from the Transtheoretical Model to assess participants' intention, based on their readiness to change their eating habits.

  7. Barriers

    Time frame: 3 test occations: baseline, 10 weeks after baseline and 5 months after baseline.

    Measured using an online questionnaire specifically developed for this study. This section of the questionnaire incorporated adapted questions from the REWARD study to assess perceived barriers to eating healthy and sustainable. Responses were recorded on a 5-point Likert scale, ranging from "strongly disagree" to "strongly agree."

  8. Coocking skills

    Time frame: 3 test occations: baseline, 10 weeks after baseline and 5 months after baseline.

    Measured using an online questionnaire developed specifically for this study. This section included the food literacy behaviours tool from Begley to assess participants' cooking skills. Responses were measured using a 5-point Likert scale, ranging from "never" to "always".

  9. Weight (in kg)

    Time frame: 3 test occations: baseline, 10 weeks after baseline and 5 months after baseline.

    Measured using an online questionnaire specifically developed for this study.

  10. Lenght (in cm)

    Time frame: 3 test occations: baseline, 10 weeks after baseline and 5 months after baseline.

    Measured using an online questionnaire specifically developed for this study.

Secondary outcomes

  1. Fidelity

    Time frame: 10 weeks after baseline

    Measured using an online questionnaire specifically developed for this study, along with additional focus group discussions with students and stakeholders.

    The questionnaire will incorporate six elements of the Saunders Framework on process evaluation of interventions, assessing various aspects of the intervention process.

  2. Dose delivered

    Time frame: 10 weeks after baseline

    Measured using an online questionnaire specifically developed for this study, along with additional focus group discussions with students and stakeholders.

    The questionnaire will incorporate six elements of the Saunders Framework on process evaluation of interventions, assessing various aspects of the intervention process.

  3. Dose received

    Time frame: 10 weeks after baseline

    Measured using an online questionnaire specifically developed for this study, along with additional focus group discussions with students and stakeholders.

    The questionnaire will incorporate six elements of the Saunders Framework on process evaluation of interventions, assessing various aspects of the intervention process.

  4. Reach

    Time frame: 10 weeks after baseline

    Measured using an online questionnaire specifically developed for this study, along with additional focus group discussions with students and stakeholders.

    The questionnaire will incorporate six elements of the Saunders Framework on process evaluation of interventions, assessing various aspects of the intervention process.

  5. Recruitment

    Time frame: 10 weeks after baseline

    Measured using an online questionnaire specifically developed for this study, along with additional focus group discussions with students and stakeholders.

    The questionnaire will incorporate six elements of the Saunders Framework on process evaluation of interventions, assessing various aspects of the intervention process.

  6. Context

    Time frame: 10 weeks after baseline

    Measured using an online questionnaire specifically developed for this study, along with additional focus group discussions with students and stakeholders.

    The questionnaire will incorporate six elements of the Saunders Framework on process evaluation of interventions, assessing various aspects of the intervention process.

  7. Sales figures collection

    Time frame: From baseline through study completion, up to 9 months.

    Sales figures in the student restaurant are continuously monitored throughout the intervention using the cash register system to track changes in purchasing behavior.

Study contacts

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

Maxine Vanhove

CONTACT

[email protected]

+32 471330330

Tom Deliens

CONTACT

[email protected]

+32 472867516

Sponsors and collaborators

Lead sponsor

Vrije Universiteit Brussel

Other

Collaborators

  • Stichting tegen Kanker
  • University Ghent
  • Vlaams Instituut Gezond Leven VZW

Registry information

Official study title

Implementation and Evaluation of Two Multicomponent Nutrition Interventions in Higher Education Students

Acronym: EATFITS

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Mar 14, 2025
Registry last updated
Apr 1, 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.