- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03233425
Evaluation of Multiprofessional Group Programs for Paediatric Obesity Therapy (KIDSSTEP)
Evaluation of Therapy for Overweight Children and Adolescents in Switzerland: Therapy in Multiprofessional Group Programs - Part 2, Collection and Analysis of Data
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In Switzerland, the number of overweight children <18 years is estimated to 80'000 and related cardiovascular, osteoarticular and other complications are already present in approximately in 50% of these youth. Controlled studies demonstrated that multiprofessional treatment programs can reduce adiposity and improve health risk factors. To pre-empt the deterioration of obesity and co-morbidities in adult life, the Swiss Department of the Interior (EDI) approved in 2007 the reimbursement of treatment of overweight children by health insurances , if conducted in certified multi-professional family-based group programs. All programs have to participate in a scientific evaluation study supported by the Federal Office of Public Health (FOPH) in order to determine nationwide outcomes in clinical practice. The goal of this study is to evaluate individual changes of physical activity, nutrition, behaviours, quality of life, co-morbidities and adiposity during therapy and to identify predictors of positive or negative changes.
During 5 years, the investigators will recruit about 200 children and adolescents aged 6 to 18 years every year. Patients must have a Body Mass Index (BMI), fat mass or waist circumference above the 97th percentile, or a BMI above the 90th percentile plus a co-morbidity. Together with their parents they will be enrolled in an intensive group therapy program for 6 to 12 months, with 12 months of follow up. To date, in 25 certified centres, physicians, nutrition and physical activity specialists as well as psychologists can provide a multiprofessional standardized care, the costs of participation being reimbursed after regular presence. At start, after 1 year and 2 years, standardized instruments validated in Swiss or European children will be used to document changes during therapy. Questionnaires will assess motivation, weight of parents, personal and family history, quality of life, child and family lifestyle, parenting skills, eating or psychological disorders, and satisfaction. Other investigations will include medical examination, blood tests, and European Fitness (*Eurofit*)-test for physical fitness and capacities. Anonymised data will be recorded centrally in an electronic database, after controlling for completeness and plausibility. Informed consent and positive votes of local ethical committees will be obtained. Reports on cross-sectional and longitudinal descriptive statistics and benchmarking will be provided once yearly. A comprehensive multivariate analysis of complex associations between predictors and health-related outcomes will be completed. Statistical analyses will be performed by specialists in each field and will be supervised by public health scientists. To guarantee meaningful analyses, the last patients will be included in December 2013.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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St. Gallen, Switzerland, 9006
- Ostschweizer Kinderspital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- BMI above the 97th percentile, or in second line waist circumference or fat mass above the nor-mal range, or BMI above the 90th percentile associated with the presence of co-morbidities
- Medical examination is a pre-requisite
- Motivation of the patient and support by the family are pre-requisites
- Psychiatric diseases or severe psychosocial restraints must be adequately tackled.
- Informed consent of patients and parents to the participation in an anonymous evaluation,
Exclusion Criteria:
- healthy child
- no motivation for therapy, as assessed by interview and questionnaires to Patient and Family
- psychiatric disease without adequate treatment
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body mass index - standard deviation score (*SDS*), (*BMI-SDS*)
Time Frame: 2 years
|
Age- and sex-adjusted BMI according to World Health Organisation (*WHO*) charts used in Switzerland
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of life as assessed by Quality of life questionnaires for children and adolescents (*KIDSSCREEN*) with 52 questions
Time Frame: 2 years
|
Outcome Measure is a Scale
|
2 years
|
|
Eurofit - Test
Time Frame: 2 years
|
Outcome measure is a score on physical fitness and sport activity of children and adolescents
|
2 years
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Dagmar lAllemand, Pr, Ostschweizer Kinderspital, St. Gallen, Switzerland
Study record dates
Study Major Dates
Study Start
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- EKSG 08/023
- 09.004211/204.0001/-629 (Other Grant/Funding Number: FOPH, CH (www.aramis.admin.ch))
- l'Allemand, 20110901 (Other Grant/Funding Number: Wyeth Stiftung, Zug)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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