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Effectiveness of an App for Mobile Phones (e-12HR) to Increase Adherence to Mediterranean Diet in University Students

NCT05532137 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 322

Last updated 2024-12-24

No results posted yet for this study

Summary

This is a controlled, randomized and multicentric clinical trial aimed at university students and performed at the Faculties of Medicine and Pharmacy at the University of Seville (Spain). Its objective is to evaluate the effect of an intervention based on the use of an information and communication technology (ICT) tool, specifically an application for mobile telephones (called e-12HR), in the improvement of adherence to the Mediterranean diet.

Conditions

  • Mediterranean Diet
  • Diet Habits
  • Healthy Eating Index

Interventions

BEHAVIORAL

e-12HR app

The 'feedback' e-12HR version: This version of the application allows to calculate the Mediterranean Diet Serving Score (MDSS) index; additionally, this version is designed to promote the Mediterranean diet with two specific automatic functions: 1. Evaluation of the user's MDSS index. 2. Identification of the food groups for which the user has not fulfilled the Mediterranean diet recommendations (in addition, this version also provided the user the consumption recommendations established for these food groups).

Sponsors & Collaborators

  • Luis María Béjar Prado

    lead OTHER

Principal Investigators

  • Luis M Bejar, Doctor · Lecturer (Department of Preventive Medicine and Public Health)

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2022-04-04
Primary Completion
2024-12-16
Completion
2025-12-16

Countries

  • Spain

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 NCT05532137 on ClinicalTrials.gov