LIVELY: MuLtidimensional School-based and Family interVentions to Promote hEalthy and Sustainable LifestYle for the Childhood

Sponsor
Mario Negri Institute for Pharmacological Research (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05966051
Collaborator
University of Pavia (Other)
300
21

Study Details

Study Description

Brief Summary

Childhood obesity condition has increased 10 times in the last 40 years, representing one of the most important public health challenges of our century.

The overweight and obesity in children are conditions associated with several determinants, mostly related to dietary habits, physical activity, and environmental behavior.

To counteract childhood obesity, several prevention programs have been promoted, however evidence concerning their efficacy was contrasting, especially among the younger population and in the long term.

Moreover, due to the wide variety of interventions administered it is not clear which specific strategy (or combinations of strategies) was the most effective.

The LIVELY study aims 1) to assess the prevalence and the factors associated to childhood overweight and obesity; 2) to develop multidimensional strategies for prevention of childhood obesity by involving families and recognizing the role of schools as an environment for raising awareness on healthy and sustainable dietary patterns and lifestyle.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Educational interventions

Detailed Description

LIVELY is a study with a one group pre-test - post-test design (without control). The study will be conducted in the primary schools of the Istituto Luigi Cadorna in Milano (Lombardy Region, Northern Italy). The study population will involve children (6-11 years) belonging to different socioeconomic status and ethnic groups, attending classes of the school whose teachers will accept to participate.

The educational interventions will consist in:

Study Design

Study Type:
Observational
Anticipated Enrollment :
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
MuLtidimensional School-based and Family Involved interVentions, to Promote a hEalthy and Sustainable LifestYle for the Childhood Obesity Primary Prevention: the LIVELY Study
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Oct 1, 2024
Anticipated Study Completion Date :
Jun 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Children attending primary school

In this study will be included children 6-11 years and their families, whose parents will provide written consent to participate,

Behavioral: Educational interventions
The educational interventions will consist in:

Outcome Measures

Primary Outcome Measures

  1. Investigate prevalence of childhood overweight and/or obesity [Baseline]

    Weight and height will be combined to report BMI in kg/m^2

  2. Investigation on adherence to Mediterranian diet [Baseline]

    Mediterranean Diet Quality Index for children and adolescents (KIDMED) will be used. The index ranges from 0 to 12 and is based on 16 questions. The sums of the values from the test are classified into three levels: scores ≥8 are considered optimal, 4-7 as average Mediterranean Diet adherence, and ≤3 as very low diet quality.

  3. Assessment of the consumption of ultra-processed food by children [Baseline]

    NOVA classification, which will classify ultra-processed foods in four groups according to their level of processing (Group 1: unprocessed foods - Group 4: ultra-processed foods)

  4. Investigation of family lifestyles [Baseline]

    Children Feeding Questionnaire (CFQ) will be used. It measures parental feeding practices and attitudes. The CFQ contains originally 31 items and measures the following seven factors: Perceived Responsibility (three items), Parent Perceived Weight (four items), Perceived Child Weight (six items), Parents Concern about Child Weight (three items), Parents' feeding practices: Restriction (eight items), Pressure to Eat (four items), and Monitoring (three items). The responses to all items are coded on a 5-point Likert scale ranging from one to five.

Secondary Outcome Measures

  1. Feasibility of multidimensional school-based educational interventions [6 months]

    Perception of usefulness of the interventions: appreciation questionnaires to investigate the satisfaction of the implemented activities; organization of the interventions and usefulness of the educational interventions

  2. Investigation of changes in adherence to Mediterranian diet [Baseline, 6 and 12 months]

    Mediterranean Diet Quality Index for children and adolescents (KIDMED) will be used. The index ranges from 0 to 12 and is based on 16 questions. The sums of the values from the test are classified into three levels: scores ≥8 are considered optimal, 4-7 as average Mediterranean Diet adherence, and ≤3 as very low diet quality.

  3. Assessment of changes of the consumption of ultra-processed food by children [Baseline, 6 and 12 months]

    NOVA classification, which will classify ultra-processed foods in four groups according to their level of processing (Group 1: unprocessed foods - Group 4: ultra-processed foods)

  4. Investigation of changes of family lifestyles [Baseline, 6 and 12 months]

    Children Feeding Questionnaire (CFQ) will be used. It measures parental feeding practices and attitudes. The CFQ contains originally 31 items and measures the following seven factors: Perceived Responsibility (three items), Parent Perceived Weight (four items), Perceived Child Weight (six items), Parents Concern about Child Weight (three items), Parents' feeding practices: Restriction (eight items), Pressure to Eat (four items), and Monitoring (three items). The responses to all items are coded on a 5-point Likert scale ranging from one to five.

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 11 Years
Sexes Eligible for Study:
All
Inclusion Criteria:
  • children 6-11 years

  • children whose parents will provide written consent to participate.

Exclusion Criteria:
  • Children who do not have inclusion criteria.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Mario Negri Institute for Pharmacological Research
  • University of Pavia

Investigators

  • Principal Investigator: Carlotta Franchi, PhD, Mario Negri Institute for Pharmacological Research
  • Principal Investigator: Marta Baviera, PharmDr, Mario Negri Institute for Pharmacological Research
  • Principal Investigator: Maria Vittoria Conti, MSc, University of Pavia

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mario Negri Institute for Pharmacological Research
ClinicalTrials.gov Identifier:
NCT05966051
Other Study ID Numbers:
  • IRFMN-8979
  • F13C22001210007
First Posted:
Jul 28, 2023
Last Update Posted:
Jul 28, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Mario Negri Institute for Pharmacological Research
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 28, 2023