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EYTO (European Youth Tackling Obesity): A Randomized Controlled Trial in Catalonia (Spain)

A Youth Led Social Marketing Campaign to Encourage Healthy Lifestyles. EYTO (European Youth Tackling Obesity): A Randomized Controlled Trial in Catalonia (Spain)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02157402
Acronym
EYTO-SPAIN
Enrollment
400
Registered
2014-06-06
Start date
2014-05-31
Completion date
2015-09-30
Last updated
2021-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Life Style, Obesity

Keywords

Adolescent

Brief summary

Our hypothesis is that healthy lifestyles improvement by an intervention designed according 8 social marketing Benchmark criteria, can reduce overweight or obesity implemented by adolescents on their colleges. The general aim of EYTO program is to improve health and well-being among adolescents who live in low socioeconomically communities, through an intervention study designed by selected adolescents with the inclusion of social marketing Benchmark criteria.

Detailed description

5 adolescent coordinators (of intervention high-schools) will be trained by experts in social marketing and health promotion. This 5 selected adolescent as coordinators who will be in charge of the design of an 8 social marketing criteria intervention to implement their peers´ lifestyles. The program has over two academic years. The participants will be followed for the duration of 2 academic years, an expected of up to 16 months.

Interventions

BEHAVIORALSocial marketing activities and pop-up events to promote healthy lifestyles

Sponsors

European Commission
CollaboratorOTHER
Centro Tecnológico de Nutrición y Salud
CollaboratorOTHER
Hospital Universitari Sant Joan de Reus
CollaboratorOTHER
Companhia de Ideas
CollaboratorUNKNOWN
Komunikujeme
CollaboratorOTHER
National Children's Bureau
CollaboratorUNKNOWN
University Rovira i Virgili
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
13 Years to 17 Years
Healthy volunteers
Yes

Inclusion criteria

* Informed consent signed by parents and/or guardians. * Adolescents between 13 and 17 years old.

Exclusion criteria

\- The lack of one or more inclusion criteria.

Design outcomes

Primary

MeasureTime frameDescription
Change of Fruit intakeChange from Baseline in fruit Intake at 2 academic yearsHealth Behaviour in School-aged Children (HBSC) survey
Change of Vegetable intakeChange from Baseline in vegetable Intake at 2 academic yearsHealth Behaviour in School-aged Children (HBSC) survey
Change of Physical activity practiceChange from Baseline in physical activity practice at 2 academic yearsHealth Behaviour in School-aged Children (HBSC) survey

Secondary

MeasureTime frameDescription
Change of Sedentary behaviourChange from Baseline in sedentary behaviour at 2 academic yearsHealth Behaviour in School-aged Children (HBSC) survey

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026