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Lifestyle Intervention in Obese Children Attending Special Primary Education.

U

University College of Antwerp

Status and phase

Unknown
Phase 2
Phase 1

Conditions

Overweight
Obesity

Treatments

Behavioral: lifestyle intervention (diet and physical activity)

Study type

Interventional

Funder types

Other

Identifiers

NCT00349232
HA-KINE-2006-001

Details and patient eligibility

About

The purpose of this study is to assess the prevalence of overweight and obesity in children attending special primary education and to evaluate the effects of a multidisciplinary school-based lifestyle intervention.

Full description

Lifestyle changes related to high-fat diets and low levels of physical activity have resulted in a rising prevalence of overweight and obesity in children and adolescents. Ten per cent of the world's school-aged children are estimated to have excess body fat. Overweight and obesity during childhood and adolescence tend to continue into adulthood, increasing the likelihood of a range of impaired health conditions including cardiovascular diseases, diabetes and some cancers. School-based interventions have been proposed to prevent or treat obesity and have been described as a promising approach to reducing obesity among youth. First the extent and the characteristics of the problem have to be assessed for different types of education.

Comparison(s): the prevalence of overweight and obesity in special primary education will be compared to the prevalence in regular primary education. In special primary education, obese and overweight children will be randomised into a experimentel group (6 months of lifestyle intervention including diet and physical activity) and a control group (6 months normal treatment, if any, e.g. exercises for motor skills).

Sex

All

Ages

6 to 14 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • children attending special and regular primary education

Exclusion criteria

  • endocrine conditions affecting bodyweight (e.g. thyroid disease, diabetes)
  • mental or physical disabilities that make it impossible to participate in sports activities

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Central trial contact

Dirk Vissers

Data sourced from clinicaltrials.gov

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