Implementation and Evaluation of Nutrition Interventions

NCT06876272 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 653

Last updated 2025-04-01

No results posted yet for this study

Summary

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.

Conditions

  • Healthy Participants
  • Nutrition Intervention
  • Higher Education Students

Interventions

BEHAVIORAL

Healthy eating promoting programme

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.

Sponsors & Collaborators

  • University Ghent

    collaborator OTHER
  • Stichting tegen Kanker

    collaborator OTHER
  • Vlaams Instituut Gezond Leven VZW

    collaborator UNKNOWN
  • Vrije Universiteit Brussel

    lead OTHER

Principal Investigators

  • Tom Deliens · Vrije Universiteit Brussel

  • Wendy Van Lippevelde · University Ghent

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Max Age
24 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-02-17
Primary Completion
2025-02-17
Completion
2025-12-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06876272 on ClinicalTrials.gov