- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04902677
Parental Perception of Child's Weight and Childhood Obesity (PERCEPS)
December 10, 2021 updated by: Fundació Sant Joan de Déu
Relationship Between Parental Perception of Child's Weight and Feeding Practices in the Context of Childhood Obesity: The PERCEPS Study
The increasing prevalence of metabolic diseases requires new strategies in the treatment and prevention of obesity.
Children exposed to a poor diet and a sedentary lifestyle are especially vulnerable and may therefore be at risk of obesity at a very early stage in their lives.
Recent studies have indicated a notable misperception of children's weight by parents.
The main objective of this project is to study the association between parental perception of child's body weight and 1) feeding practices (permissive, restrictive or model); and 2) child's degree of overweight.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
4000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Carles Lerin, PhD
- Phone Number: (+34) 936009751
- Email: clerin@fsjd.org
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
4 years to 8 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The population consists in children from the 22 schools in the Sant Boi municipality (Barcleona, Spain).
There are 5000 children of age beween 4-8 in these schools.
Description
Inclusion Criteria:
- Willing to participate
Exclusion Criteria:
-
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
School
|
No intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Infant feeding practices measured by the Child Feeding Practice questionnaire
Time Frame: Baseline
|
We will assess three factors from the Child Feeding Practice (CFP) questionnaire measuring parental control practices and attitudes regarding child feeding: Restriction (8 items), Pressure to eat (4 items), and monitoring (3 items).
Each item is scored from 1 to 5, and the mean value for each factor will be calculated.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Participant BMI z-score
Time Frame: Baseline
|
Weight and height of participants will be measured and combined to calculate the BMI z-score based on the WHO growth charts
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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 (Anticipated)
January 1, 2022
Primary Completion (Anticipated)
June 1, 2022
Study Completion (Anticipated)
June 1, 2022
Study Registration Dates
First Submitted
May 20, 2021
First Submitted That Met QC Criteria
May 25, 2021
First Posted (Actual)
May 26, 2021
Study Record Updates
Last Update Posted (Actual)
December 13, 2021
Last Update Submitted That Met QC Criteria
December 10, 2021
Last Verified
December 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PERCEPS
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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