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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: Netherlands Trial Register
Last refreshed on: 28 April 2013
Main ID:  NTR811
Date of registration: 17/11/2006
Primary sponsor: Erasmus Medical Center
Public title: VETisnietVET / FATaintPHAT
Scientific title: ?VETisnietVET.nl?: The impact of a web-based interactive computer tailored intervention on weight gain related behaviours in youth?. - N/A
Date of first enrolment: 1/6/2006
Target sample size: 1200
Recruitment status: recruiting
URL:  http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=811
Study type:  intervention
Study design:  Randomised: Yes; Masking: None; Control: Not applicable; Group: Parallel; Type: -  
Countries of recruitment
The Netherlands
Contacts
Name: Nicole  Ezendam
Address:  Erasmus Medical Center, Department of Public Health, Room AE-139, P.O. Box 2040 3000 CA Rotterdam The Netherlands
Telephone: +31 (0)10 4089253
Email: n.ezendam@erasmusmc.nl
Affiliation: 
Name: Anke  Oenema
Address:  Erasmus Medical Center, Department of Public Health, Room AE124, P.O. Box 2040 3000 CA Rotterdam The Netherlands
Telephone: +31 (0)10 4087718 / 4638475
Email: a.oenema@erasmusmc.nl
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: Secondary schools (locations) in the municipal health organization regions: Rotterdam and surrounding areas and Nieuwe Waterweg Noord.
Exclusion criteria: 1. Schools (locations) where pupils have very low reading capacity (i.e. pupils that are not able to fill in a questionnaire);
2. Schools (locations) that offer special sports education (i.e. special sports schools);
3. Schools (locations) where the pupils could not be followed-up to the third year, i.e. schools that only provide education for the first two years of secondary education (onderbouw) and where the pupils could not be tracked to other.


Age minimum:
Age maximum:
Gender:
Health Condition(s) or Problem(s) studied
No condition, healthy person

Intervention(s)
Intervention group:
The pupils in the intervention schools will use a computer-tailored intervention on weight gain related behaviours (physical activity, sedentary behavior, snack, fruit and vegetable, fiber and soft-drink consumption) during their first year of secondary school. The intervention will be used during school hours as part of the education program. The intervention will be used for an average of 2 hours (preferably divided by 8 times 15 minutes) within 10 subsequent weeks.

Control group:
The control group will receive regular school lessons. After two years the intervention will be available for the control group as well.
Primary Outcome(s)
BMI calculated from measured height and weight, at baseline and 2 year follow-up
Waist circumference measured between hipbone and lowest rib, at baseline and 2 year follow-up.
Secondary Outcome(s)
1. Physical activity measured with self-report questionnaires plus pedometer counts (for part of the participants) at baseline, three months and 2 year follow-up;
2. Physical condition measured with a shuttle-run-test at baseline and 2 year follow-up;
3. Various dietary sub-behaviors, i.e. fruit and vegetable consumption, soft-drink consumption, snack consumption and fiber consumption measured with self-report questionnaires at baseline, three months and 2 year follow-up;
4. Amount of television viewing / time spend with the computer measured with self-report questionnaires at baseline, three month and 2 year follow-up;
5. Awareness of personal bodyweight status, overweight-related risk perceptions, weight maintenance attitudes, perceived behavioral control, and motivation to engage in weight maintenance behaviors, measured with self-report questionnaires at baseline, three months and 2 year follow-up;
6. Determinants of change for the separate dietary, physical activity and sedentary behaviors, as measured by self-report questionnaires, distributed at baseline, three months and two year follow-up.
Secondary ID(s)
Application number ZonMw: 3138
ISRCTN15743786
Source(s) of Monetary Support
ZON-MW, The Netherlands Organization for Health Research and Development
Secondary Sponsor(s)
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