- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05858697
Weight Development in Children With Obesity After Declining Treatment
Weight Development in Children With Obesity After Declining Participation in a Community-based Lifestyle Intervention.
Childhood obesity is a major health concern and lifestyle intervention is recommended as the cornerstone in the weight loss treatment. However, only limited knowledge exists in relation to characterization and follow-up of children who decline participation in a lifestyle intervention. The aim of this study is to investigate the long-term development in BMI z-score for children with obesity who decline to participate in a lifestyle intervention.
This study identified approximately 170 children with obesity who declined treatment in a community-based lifestyle intervention. The development in BMI z-score for these children will be compared to children enrolled in the lifestyle intervention (i.e. treatment) and children who were never invited.
Data from different sources will be used to answer the research question (intervention registries, health check-ups at school and Danish registries).
Study Overview
Status
Conditions
Detailed Description
Childhood obesity has been associated with increased risk of poorer mental health, later non-communicable lifestyle diseases (e.g. prediabetes, sleep apnea), and of continued excess body weight into adulthood. Multi-component family-centered lifestyle intervention seems to be the cornerstone in the treatment. However, only limited knowledge exists regarding weight development in children with obesity who decline to participate in such a lifestyle intervention. The aim of this study is therefore to investigate the long-term development in BMI z-score in children with obesity from 5 to 7 years of age who declined to participate in a lifestyle intervention. The development in BMI z-score for these children will be compared to children accepting the treatment and children who were never invited. A secondary aim is to investigate the potentially modifying effects of socioeconomic status (SES).
The participants:
This cohort study will include children from the city of Aarhus with a baseline visit between January 1st 2010 and June 30th 2020 children. The inclusion criteria are 1) 5-7 years of age and 2) obesity at baseline. Obesity will be defined by the International Obesity Task Force (IOTF) as BMI ≥ 30kg/m2 for age and gender. BMI z-score will be calculated be external reference population (WHO).
The expected number of children included:
- App. 150-170 children with obesity who declined to participate in the Aarhus intervention (Declining group).
- App. 400 children with obesity accepted participation and received treatment in a multicomponent family-centered lifestyle intervention (intervention group).
- App. 700-800 children with obesity living in Aarhus, who were not invited to participate in the lifestyle intervention (Non-intervention group)
Data sources:
- Participants will be identified using data from the municipality register.
- Anthropometrical data will be extracted from TM-Sund (Aarhus). TM-Sund is a database used to store data on anthropometrics obtained at health checks by specialized school nurses, Denmark.
- Data on SES, immigration and psychiatric illness will be obtained from Danish National registries.
Statistics:
A multiple imputation (MI) with chained equations will be applied to replace missing data regarding socioeconomic status and immigration, if missing data causes the models to lose substantial amount of observations, m=100. An adjusted mixed effects model with splines will be used to describe the development in BMI z-score for children declining participation and compare those to the reference and to the intervention groups. Knots will be placed at baseline and after ½, 1, 3 and 10.5 year. The model will be adjusted for age, BMI z-score, gender, family type, highest completed household education, equalized household income, immigration status, psychiatric diagnosis and psychiatric diagnosis (parents), zip code / distance to treatment center at baseline.
Ethics & permissions:
The local health ethics committee has approved the project, including data transfer (rec.no 1-45-70-27-20).
The project is internally reported to the University of Aarhus (rec no. 2916) The project has achieved approval from The Danish Data Protection Agency and the Principal Investigator has been granted accessed to register data from Statistics Denmark.
A full plan for analytics has been completed.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Aarhus N, Denmark, 8200
- Steno Diabetes Center Aarhus
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- 5-7 years of age
- obesity at baseline as defined by the International Obesity Task Force (IOTF) as BMI ≥ 30kg/m2 for age and gender.
Exclusion Criteria:
- More than 6 months between a baseline visit and the next observation with a BMI z score
- First declining and subsequently accepting the intervention.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Declining group
Children with obesity 5-7 years of age who were invited to the intervention but declined participation.
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Each year a fraction of the children invited into the Aarhus intervention decline to participated.
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Interventions group
Children with obesity 5-7 years of age who accepted and subsequently received treatment.
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A community-based multicomponent family-centered lifestyle intervention which included visits at home and weekly supervised physical activity.
The intervention has a maximum duration of one year.
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'Non intervention' group
Children with obesity at age 5-7 years living in Aarhus, who were never invited to participate in the lifestyle interventions.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The annual change in BMI z-score from baseline for children with obesity declining a lifestyle intervention and the difference in the annual change in BMI z-score compared to children in the intervention and the no-intervention group.
Time Frame: Baseline visit between 1st of January 2010 to 30th of June 2020.
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The annual change in BMI z-score from baseline will be modelled by using a mixed effect model with splines and be compared 1) to children accepting the treatment and 2) to children who were never invited to participate.
These models will be displayed as both crude analyses and adjusted for child and parent's characteristics at baseline
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Baseline visit between 1st of January 2010 to 30th of June 2020.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Different associations of the annual change in BMI z-score in subgroups (immigration and socioeconomic status) of children declining the intervention compared to children in the intervention and the no-intervention group,
Time Frame: Baseline visit between 1st of January 2010 to 30th of June 2020.
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A modification analysis will be applied by adding the dichotomized variables income (dichotomized by the median), education (≤12 vs ≥13 years of education) and immigration status (Danish origin vs immigrant) as interactions term to the mixed model.
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Baseline visit between 1st of January 2010 to 30th of June 2020.
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022-0367531, 2916
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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