CClinicalTrials.gg
CompletedNCT04915092CoSIEUpdated Jun 25, 2025

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

An interventional study of CoSIE app in Childhood Obesity, sponsored by Azienda USL Reggio Emilia - IRCCS. Completed at 1 site in Italy. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-06-25.

Sponsored by Azienda USL Reggio Emilia - IRCCS · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
327
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Childhood Obesity

Keywords

  • mhealth
  • app
  • obesity
  • prevention
03

In context

Pediatric Obesity

1,117 studies on the registry are indexed under Pediatric Obesity; 189 are open to participants now.

This study's enrollment of 327 is above the median of 103 across 862 interventional studies indexed under Pediatric Obesity.

Browse Pediatric Obesity studies →

Lead sponsor

Azienda USL Reggio Emilia - IRCCS is the lead sponsor of 92 studies on the registry; 25 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
327 participants (actual)

Study arms

  • 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.

    Device: CoSIE 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.

Interventions

  • DeviceCoSIE app

    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.

06

What researchers measure

Primary outcomes

  1. Change in consumption of sugar - sweetened beverages and juice, first year

    Endpoint: number per week Outcome: Delta 12m-baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits

    Time frame: 12 months

  2. Change in consumption of sugar - sweetened beverages and juice, second year

    Endpoint: number per week Outcome: Delta 24m - baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits

    Time frame: 24 months

  3. Change in consumption of hypercaloric foods like fried food, salty snacks and sweet snacks/candies, first year

    Endpoint: number per week Outcome: Delta 12m-baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits

    Time frame: 12 months

  4. Change of consumption of hypercaloric foods like fried food, salty snacks and sweet snacks/candies, second year

    Endpoint: number per week Outcome: Delta 24m-baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits

    Time frame: 24 months

  5. Change in screen time spent by children, first year

    Endpoint: Minutes of screen time per day Outcome: Delta 12m-baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits

    Time frame: 12 months

  6. Change in screen time spent by children, second year

    Endpoint: Minutes of screen time per day Outcome: Delta 24m-baseline Test/analysis: Difference between groups Source: Questionnaire in FU visits

    Time frame: 24 months

Secondary outcomes

  1. BMI centile of children after the first year

    Endpoint: BMI centile Outcome: Delta 12m-baseline Test/analysis: Difference between group means Source: FU visits

    Time frame: 12 months

  2. BMI centile of children after the second year

    Endpoint: BMI centile Outcome: Delta 24m-baseline Test/analysis: Difference between group means Source: FU visits

    Time frame: 24 months

  3. Acceptability

    How much parents accept the concept of using an app to guide their habits in children education Test/analysis: qualitative analysis Source: Interviews

    Time frame: after at 12 months of app utilization

  4. Usability

    How much each single app function is used and is perceived as useful by parents Test/analysis: qualitative analysis Source: Interviews

    Time frame: after at 12 months of app utilization

07

Study locations

1 site
  • Azienda USL-IRCCS Reggio Emilia
    Reggio Emilia, Reggio Emilia 42123, Italy
08

References and documents

Publications

  • Giorgi Rossi P, Ferrari F, Amarri S, Bassi A, Bonvicini L, Dall'Aglio L, Della Giustina C, Fabbri A, Ferrari AM, Ferrari E, Fontana M, Foracchia M, Gallelli T, Ganugi G, Ilari B, Lo Scocco S, Maestri G, Moretti V, Panza C, Pinotti M, Prandini R, Storani S, Street ME, Tamelli M, Trowbridge H, Venturelli F, Volta A, Davoli AM; Childhood Obesity Prevention Working Group. Describing the Process and Tools Adopted to Cocreate a Smartphone App for Obesity Prevention in Childhood: Mixed Method Study. JMIR Mhealth Uhealth. 2020 Jun 8;8(6):e16165. doi: 10.2196/16165. PubMed 32357123 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 25, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04915092
Lead sponsor
Azienda USL Reggio Emilia - IRCCS
Responsible party
Sponsor
First posted
Jun 7, 2021
Start date
Jun 14, 2021
Primary completion
Jan 15, 2024
Completion
Jan 15, 2024
Last update
Jun 25, 2025

Study contacts

Paolo Giorgi Rossi, phd
principal investigator · Azienda USL-IRCCS Reggio Emilia

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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