Actively Recruiting

Phase Not Applicable
Age: 11Years - 16Years
All Genders
Healthy Volunteers
ID06792461

Randomized Controlled Trial Evaluating an eHealth Platform to Promote Healthy Habits Among Adolescents in Disadvantaged Settings

Led by Fundació Sant Joan de Déu · Updated on 2026-04-29

1000

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

Sponsors

F

Fundació Sant Joan de Déu

Lead Sponsor

U

Universitat Autonoma de Barcelona

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating an eHealth platform called ePro-Schools designed to promote physical activity, healthy eating, and reduce sedentary behavior among adolescents from socially disadvantaged backgrounds in Central Catalonia. The study aims to address gaps in public health policies by co-designing the platform with adolescents, school staff, and policymakers. This randomized controlled trial will assess the program's effectiveness, cost-effectiveness, and implementation in six secondary schools with around 1000 adolescent participants. The intervention includes two digital platforms: an Intervention Platform containing interactive modules for students and physical education teachers, and an Information Platform with educational resources for students, teachers, and families. The program will be delivered during one school year (2025/26) through web-based access. Schools are randomized into an intervention group receiving full access to the platform and a control group receiving only basic health-related information, with the control group gaining access to the full platform after the trial. Participants will be evaluated at baseline, post-intervention, and nine months after post-intervention for physical activity levels, sedentary behavior, and dietary habits, which are the primary outcomes. Secondary outcomes include physical fitness, water consumption, quality of life, depressive symptoms, social isolation, and sleep quality. The study also involves surveys, questionnaires, interviews, and focus groups to monitor adoption, acceptability, and feasibility. The total participation covers the school year and follow-up period with continuous engagement and data collection.

CONDITIONS

Brief Title

ePlatform for Promoting Health in Schools

Who Can Participate

Age: 11Years - 16Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Students enrolled in 1st, 2nd, or 3rd year of secondary school (ages approximately 11-16) in Central Catalonia socially disadvantaged settings
  • All genders eligible
  • Written informed consent provided by adolescent and parent(s)/legal guardian(s)
  • Physical education teachers currently working at participating schools
  • Physical education teachers aged 18 years or older
  • Written informed consent provided by teachers
Not Eligible

You will not qualify if you...

  • Individuals (adolescents or teachers) who do not provide written informed consent

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - One school year (2025/26)

Participants will use the ePro-Schools platform to promote healthy habits during one school year. The intervention group accesses interactive modules on physical activity and nutrition, while the control group receives basic health information through an information platform.

Multiple evaluations at baseline, post-intervention, and follow-up

Follow-up

Duration - 9 months after post-intervention

Participants are evaluated nine months after the end of the school year to assess the lasting effects of the intervention on lifestyle behaviors and health outcomes.

1 visit (in-person) for follow-up evaluation

Trial Site Locations

Total: 1 location

1

Parc Sanitari Sant Joan de Déu

Sant Boi de Llobregat, Barcelona, Spain, 08242

Actively Recruiting

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Research Team

R

Rodrigo Antunes Lima, PhD

M

Mariona Perez Anton, MSc

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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