Evaluation of the Efficacy of an App for Parents to Promote Healthy Life-styles in Children: the CoSIE Trial (CoSIE)

January 30, 2024 updated by: Massimo Vicentini, Arcispedale Santa Maria Nuova-IRCCS

Co-creation of Service Innovation - Evaluation of the Efficacy of an App for Parents to Prevent Childhood Obesity and Promote Healthy Life-styles: CoSIE Randomized Controlled Trial

The objective of the study is to evaluate the effectiveness of the app in terms of changing lifestyles both related to nutrition and physical activity. The study is also aimed at evaluating the usability and the degree of acceptance of the app among parents.

The primary objective will be assessed in terms of the change in the consumption of sugary drinks and high-calorie food and in terms of time spent in front of a screen.

The secondary objectives are the evaluation of BMI (percentile and z-score) and waist circumference and the evaluation of the usability of the app.

STUDY DESIGN The study is a randomized control trial. Both parents and children are recruited.

  • Family paediatricians during the health balance of 3 or 5 years old (children between 3 and 6.5 years old)
  • Sport medicine during the visits for sport ability (children between 7 and 11 years old)
  • Pediatric Endocrinology and Diabetology of the Santa Maria Hospital during routine visits (children between 5 and 11 years old)

When the study is presented to families, few clinical information are collected on the electronic platform designed for enrollment and randomization:

  • Child weight and height
  • Child waist circumference

More information about children and parents are collected (through questionnaire).

The families (both treatment and control ) are contacted after 12 month and after 24 months from the recruitment to answer to a questionnaire on lifestyle habits (food and physical activity) of the child and app utilization

During this visit also child weight, height and waist circumference will be collected.

Intervention group The app is explained and installed during the recruitment to the family in the intervention group.

Some families in this group will be selected to take part to the qualitative research.

Control group Every months during the first year of study a newsletter is sent only to the members of the control group.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Childhood obesity is a highly prevalent condition and together with the behaviours associated with it, such as improper diet and physical inactivity, it generates a high burden of disease in adulthood.

In recent years, it is increasing the use of mobile devices in support of health prevention and promotion strategies. In a primary care setting these new technologies offer the opportunity to open a two-way communication channel between parents and institutions and can help by adapting the intervention and framing the message according to the needs of each family.

Since 2010, the Reggio Emilia AUSL has started a research and interventions program aimed at preventing childhood obesity. The program has adopted a multilevel and multi-setting strategy for primary prevention (BMInforma Program).

Since 2017, together with the University of Bologna and the regional company Lepida2000, the Local Health Authority is part of the Co-creation of Service Innovation in Europe project (CoSIE Project), a project funded by the European Union with a Horizon 2020 call coordinated by the University of Turku, Finland. The CoSIE project promotes the co-creation of public services through the involvement of citizens and other interested parties in the definition of objectives and delivery methods.

The project is divided into nine pilot projects and the Italian pilot project, carried out in the province of Reggio Emilia, is part of the AUSL program for the prevention of childhood obesity. The aim of the pilot project is to create a network between the services involved in the prevention and treatment of obesity and, at the same time, it aims to create an app that can help promote a healthy lifestyle. The app was designed and created with a co-creation process.

The objective of the study is to evaluate the effectiveness of the app in terms of changing lifestyles both related to nutrition and physical activity. Furthermore,an aim of the study is to evaluate the usability and the degree of acceptance of the app among parents.

The primary objective will be assessed in terms of the change in the consumption of sugary drinks and high-calorie food and in terms of time spent in front of a screen.

The secondary objectives are the evaluation of BMI (percentile and z-score) and waist circumference and the evaluation of the usability of the app.

STUDY DESIGN The study is a randomized control trial.

Both parents and children are recruited. The recruitment is done by some members of the CoSIE project Consulting Committee:

  • Family paediatricians during the health balance of 3 or 5 years old (children between 3 and 6.5 years old)
  • Sport medicine during the visits for sport ability (children between 7 and 11 years old)
  • Pediatric Endocrinology and Diabetology of the Santa Maria Hospital during routine visits (children between 5 and 11 years old)

When the study is presented to families, few clinical information are collected on the electronic platform designed for enrollment and randomization:

  • Child weight and height
  • Child waist circumference

More information about children and parents are collected (through questionnaire).

The families (both treatment and control ) are contacted after 12 month and after 24 months from the recruitment to answer to a questionnaire on lifestyle habits (food and physical activity) of the child and app utilization

During this visit also child weight, height and waist circumference will be collected.

Intervention group The app is explained and installed during the recruitment to the family in the intervention group.

Some families in this group will be selected to take part to the qualitative research.

Control group Every months during the first year of study a newsletter is sent only to the members of the control group.

Study Type

Interventional

Enrollment (Actual)

327

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Reggio Emilia, Italy, 42123
        • Azienda USL-IRCCS Reggio Emilia

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • parents of children aged 3 to 11 presneting for a new well child visit or for a sport medicin visit or presenting for a childhood obesity visit at the AUSL Reggio Emilia clinics, including family pediatricians clinics.

Exclusion Criteria:

  • Families resident outside the Province of Reggio Emilia
  • Parents with no comprehension of the Italian language
  • Children inside a program for obesity cure or prevention. The program are:

    • the GET program (a program coordinated by the hospital pediatric unit in which obese children follow a group intervention),
    • the BMInforma program (in which overweight girls from 5 to 7 years old follow a counselling proposed by the family paediatrician),
    • the second level medical clinic in which obese children with pathologic condition are cured
  • Children with severe obesity previously diagnosed

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention group
The app is explained and installed during the recruitment to the family in the intervention group. Some families in this group will be selected to take part to the qualitative research.

The app is a mobile phone application compatible with both iOS and Android operating system. Parents are able to register their children and to keep track of their weight status and activities. The app include five themes: child development, physical activity, healthy food, critical situations, BMI.

Push notification on healthy behaviours, on important event taking place in the province of Reggio Emilia, on food advices based on seasonality and on party tips are constantly delivered by the app.

No Intervention: Control group
Every months during the first year of study a newsletter is sent only to the members of the control group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in consumption of sugar - sweetened beverages and juice, first year
Time Frame: 12 months
Endpoint: number per week Outcome: Delta 12m-baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits
12 months
Change in consumption of sugar - sweetened beverages and juice, second year
Time Frame: 24 months
Endpoint: number per week Outcome: Delta 24m - baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits
24 months
Change in consumption of hypercaloric foods like fried food, salty snacks and sweet snacks/candies, first year
Time Frame: 12 months
Endpoint: number per week Outcome: Delta 12m-baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits
12 months
Change of consumption of hypercaloric foods like fried food, salty snacks and sweet snacks/candies, second year
Time Frame: 24 months
Endpoint: number per week Outcome: Delta 24m-baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits
24 months
Change in screen time spent by children, first year
Time Frame: 12 months
Endpoint: Minutes of screen time per day Outcome: Delta 12m-baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits
12 months
Change in screen time spent by children, second year
Time Frame: 24 months
Endpoint: Minutes of screen time per day Outcome: Delta 24m-baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits
24 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
BMI centile of children after the first year
Time Frame: 12 months
Endpoint: BMI centile Outcome: Delta 12m-baseline Test/analysis: Difference between group means Source: FU visits
12 months
BMI centile of children after the second year
Time Frame: 24 months
Endpoint: BMI centile Outcome: Delta 24m-baseline Test/analysis: Difference between group means Source: FU visits
24 months
Acceptability
Time Frame: after at 12 months of app utilization
How much parents accept the concept of using an app to guide their habits in children education Test/analysis: qualitative analysis Source: Interviews
after at 12 months of app utilization
Usability
Time Frame: after at 12 months of app utilization
How much each single app function is used and is perceived as useful by parents Test/analysis: qualitative analysis Source: Interviews
after at 12 months of app utilization

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Paolo Giorgi Rossi, phd, Azienda USL-IRCCS Reggio Emilia

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 14, 2021

Primary Completion (Actual)

December 15, 2023

Study Completion (Actual)

December 15, 2023

Study Registration Dates

First Submitted

November 16, 2020

First Submitted That Met QC Criteria

May 31, 2021

First Posted (Actual)

June 7, 2021

Study Record Updates

Last Update Posted (Actual)

January 31, 2024

Last Update Submitted That Met QC Criteria

January 30, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • ID:360 - CoSIE app

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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