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CHOKing Prevention Project

CHOKing Prevention Project

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03218618
Acronym
CHOP
Enrollment
1670
Registered
2017-07-14
Start date
2017-12-01
Completion date
2019-03-31
Last updated
2021-04-28

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

Conditions

Attitudes, Health Knowledge, Practice

Brief summary

The aim of such study is to compare three different school-based (in nurseries, kindergartens and primary schools) interventions aimed at teaching to families how to prevent food choking injuries. The topic of food choking primary and secondary prevention is placed in a more general topic regarding food safety, including education on food labeling and on food waste prevention.

Detailed description

The CHOP has been designed as a community intervention trial that compares three different school-based intervention strategies aimed at teaching to families how to prevent food choking injuries in children, together with the basics of food safety. The choice of employing such study design is motivated by the facts that community intervention trials allow to reach as many people as possible regardless their risk of experiencing the outcome of interest and to inform policy-makers on the effectiveness of an intervention on a community basis instead of an individual basis. Forty-eight educational facilities (nurseries, kindergartens and primary schools) equally distributed between North, Centre, South, and major Islands of Italy will be enrolled. Educational facilities will be stratified so that each stratum will include one educational facility from each educational stage (stratum=1 nursery, 1 kindergarten, 1 primary school). The assessment of the effectiveness of each intervention strategy will be performed through a structured telephonic interview one month after the delivery of the intervention. I Schools, to be enrolled, must provide: * availability of at least 45 families (one member from each family will be involved in the study); * availability of a room and of technological system (monitor, sound system) allowing the performance of the educational intervention; * availability of administrative support; * approval of the inclusion in the study by school's competent bodies. Family members (one from each family) must be: * aged \>18 years; * parent of children attending the school or person exercising the parental authority on children attending the school; * without physical impairments not allowing the performance of practical activities; * willing to participate at all stages of the study; * signed informed consent.

Interventions

None listed

Sponsors

University of Padova
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years

Inclusion criteria

\- Schools, to be enrolled, must provide: * availability of at least 45 families (one member from each family will be involved in the study); * availability of a room and of technological system (monitor, sound system) allowing the performance of the educational intervention; * availability of administrative support; * approval of the inclusion in the study by school's competent bodies. Family members (one from each family) must be: * aged \>18 years; * parent of children attending the school or person exercising the parental authority on children attending the school; * without physical impairments not allowing the performance of practical activities; * willing to participate at all stages of the study; * signed informed consent.

Exclusion criteria

* Schools that will not meet inclusion criteria will not be enrolled in the study. Family members who will not meet the inclusion criteria will not be involved in the study.

Design outcomes

Primary

MeasureTime frameDescription
percentage of correct answers to telephonic structured interviewup to 30 days after the interventionpercentage (%)

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026