Actively Recruiting

Phase Not Applicable
Age: 10Years - 13Years
All Genders
ID06792981

Effectiveness and Cost-effectiveness of an Online School-based Program to Reduce Eating Disorder Risk in Pre-Adolescents (PRETA)

Led by Servicio Canario de Salud · Updated on 2025-09-19

1068

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

S

Servicio Canario de Salud

Lead Sponsor

U

University of La Laguna

Collaborating Sponsor

AI-Summary

What this Trial Is About

Eating disorders are mental health conditions marked by unhealthy behaviors around food and weight control, often affecting pre-adolescents in developed countries. This research aims to develop and evaluate the PRETA program, an online school-based intervention designed to reduce eating disorder risks and modifiable factors. The study uses a randomized controlled trial to compare the PRETA program with regular school health activities, assessing its effectiveness and social impact. The PRETA program involves nine weekly online sessions lasting 45 minutes each, focusing on healthy eating habits, body image, media literacy, and psychological skills such as self-esteem and emotional regulation. It includes education for students as well as training and resources for their parents and teachers. Schools are randomly assigned to either receive the PRETA program or continue usual health activities, with six schools in each group. Participants will complete baseline questionnaires before starting the program and follow-up assessments immediately after. Researchers will evaluate outcomes like eating attitudes using the Children's Eating Attitudes Test (ChEAT-26), body image, self-esteem, and the influence of media and social pressures. The study monitors adherence through teacher follow-ups and parent reminders, with the intervention lasting three months and outcomes assessed at the program's end.

CONDITIONS

Brief Title

Evaluation of a Digital School-Based Intervention for the Primary Prevention of Eating Disorders in Pre-Adolescents (PRETA Program)

Who Can Participate

Age: 10Years - 13Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Enrolled in the fifth or sixth year of primary education
  • Informed consent provided by the student's legal guardians and responsible teacher to participate
Not Eligible

You will not qualify if you...

  • Significant comprehension difficulties that limit adequate participation in the program and questionnaires

AI-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 or remote) for consent and baseline assessment

Intervention

Duration - 3 months

Participants in the intervention group engage in the PRETA program, which includes 9 online sessions of 45 minutes each over 3 months, with weekly platform-guided classroom activities and optional at-home activities. Parents and teachers receive targeted training and resources to support prevention efforts.

Weekly activities through an online platform with minimal teacher interaction

Post-intervention Assessment

Duration - Immediately after the intervention

After completing the program, participants complete questionnaires to assess eating attitudes, body image, body dissatisfaction, internalization of appearance ideals, and self-esteem.

1 visit to complete outcome questionnaires

Trial Site Locations

Total: 1 location

1

Servicio de Evaluación y Planificación del Servicio Canario de Salud

Santa Cruz de Tenerife, Santa Cruz de Tenerife, Spain, 38109

Actively Recruiting

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Research Team

Y

Yolanda Ramallo-Fariña, PhD in Biomedical Sciences

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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Published Research Related To This Trial

Effectiveness and cost-effectiveness of an online school-based programme to reduce eating disorder risk factors in preadolescents (PRETA): protocol for a cluster-randomised controlled trial.

Yolanda Ramallo-Fariña, Tasmania Del Pino-Sedeño, Berta Pinto Robayna...

https://pubmed.ncbi.nlm.nih.gov/41087111