Actively Recruiting

Phase Not Applicable
Age: 7Years - 19Years
All Genders
Healthy Volunteers
NCT07385820

A Comparative Intervention Study on Strategies for Fruit Distribution and Awareness Campaigns in Schools

Led by Karolinska Institutet · Updated on 2026-02-06

300

Participants Needed

2

Research Sites

50 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This implementation study evaluates two strategies to increase fruit consumption among Swedish students. (1) installing fruit stands in schools and (2) combining fruit stands with a health-awareness campaign. The intervention is implemented in a set of participating schools, each following one of the predefined strategies. Students are asked to use a research app to photograph their meals and snacks during three data-collection periods before, during, and after the intervention. The study collects information on fruit intake, eating patterns, and the number of fruits taken from the stands to assess effectiveness and reduce food waste. The aim is to identify which strategy better supports healthy eating habits in school environments.

CONDITIONS

Official Title

A Comparative Intervention Study on Strategies for Fruit Distribution and Awareness Campaigns in Schools

Who Can Participate

Age: 7Years - 19Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Students enrolled in a Swedish school (elementary, middle, or high school)
  • Ages 7 to 19 years
  • Able to use a mobile phone to document meals and snacks
  • Provided informed consent (parental consent required if under 15 years old)
Not Eligible

You will not qualify if you...

  • Presence of any clinically significant disease or condition that may interfere with participation or affect study outcomes

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Internationella Engelska Gymnasiet Södermalm

Stockholm, Sweden, 118 58

Actively Recruiting

2

Blackebergs gymnasium

Stockholm, Sweden, 168 48

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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