The Activity School in Finnmark for Overweight Children
11 de diciembre de 2014 actualizado por: University Hospital of North Norway
The Activity School in Finnmark for Overweight and Obese Children and Their Families
The purpose of this study is to evaluate the effectiveness of a life style counseling programme designed for overweight and obese children and their parents in groups compared to traditional individual counseling in the pediatric outpatient clinic and the community.
The two interventions are both hospital and community based.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Descripción detallada
Randomized study design with two parallel groups.Active intervention in two years, last follow-up after 3 years.
Tipo de estudio
Intervencionista
Inscripción (Actual)
97
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
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Hammerfest, Noruega, 9600
- Childrens departement Finnmark Hospital, Norway
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
6 años a 12 años (Niño)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Todos
Descripción
Inclusion Criteria:
- Overweight or obese.
- BMI > IOTF (International Obesity TaskForce) cut-points 27,5. kg/ m2.
Exclusion Criteria:
- Diseases not compatible with normal physical activity.
- Disorders not compatible with group treatment.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Group intervention
Lifestyle counseling (physical activity and dietary modification) in groups both at the hospital and in their own municipality.
They meet a multidisciplinary team, receive organized physical activity in the municipality and are invited to a 3 days camp after 4-6 months.
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The activity school in Finnmark. Lifestyle counseling (physical activity and dietary modification) in groups both at the hospital and in their own municipality. They meet a multidisciplinary team, receive organized physical activity in the municipality and are invited to a 3 days camp after 4-6 months.
Conventional lifestyle counseling individually by single health professionals, both in hospital and in municipality.
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Comparador activo: Individual intervention
Lifestyle counseling for each separate family practiced by single health professionals both in hospital and municipality.
A more conventional model.
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Conventional lifestyle counseling individually by single health professionals, both in hospital and in municipality.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in Body Mass Index compared to baseline
Periodo de tiempo: 3 years
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BMI will be measured at baseline and at 3 months- , 1 year-, 2 year- and 3-year follow-up.
Primary measures at 2 years of continuous lifestyle modification.
Last measurement at 1 year after last counselling and active treatment has stopped, 3 years from baseline.
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3 years
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in Systolic Blood Pressure compared to baseline
Periodo de tiempo: 3 years
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Measured with an automated blood pressure monitor at baseline, at 3 months- , 1 year-, 2 year- and 3-year follow-up.
Primary measures at the end (2 years) of continuous lifestyle modification.
Last measurement at 1 year after last counseling and active treatment has stopped, 3 years from baseline.
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3 years
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Change in Body fat compared to baseline
Periodo de tiempo: 3 years
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Measured with bioelectrical impedance analysis at baseline and at 3 months- , 1 year-, 2 year- and 3-year follow-up.Primary measures at 2 years of continuous lifestyle modification.
Last measurement at 1 year after last counseling and active treatment has stopped, 3 years from baseline.
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3 years
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Change in activity level / Counts per min compared to baseline
Periodo de tiempo: 3 years
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Measured with accelerometers at baseline, 1 year-, 2 year- and 3-year follow-up.
Primary measures at 2 years of continuous lifestyle modification.
Last measurement at 1 year after last counseling and active treatment has stopped, 3 years from baseline.
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3 years
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Change in Waist circumference compared to baseline
Periodo de tiempo: 3 years
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Measured with measuring tape mid-point between the lowest rib and the top of the iliac crest at baseline, 3 months- , 1 year-, 2 year- and 3-year follow-up.
Primary measures at 2 years of continuous lifestyle modification.
Last measurement at 1 year after last counseling and active treatment stopped, 3 years from baseline.
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3 years
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Change in Homa Score / HOMA IR compared to baseline
Periodo de tiempo: 3 years
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Homa score calculated from the cross product of fasting plasma insulin and plasma glucose divided with a factor of 22.5.
Fasting plasma insulin and glucose will be measured at baseline, at 1 year-, 2 year- and 3-year follow-up.
Primary measures at 2 years of continuous lifestyle modification.Last measurement at 1 year after last counseling and active treatment has stopped, 3 years from baseline.
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3 years
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Change in triceps skinfold compared to baseline
Periodo de tiempo: 3 years
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Measured with Holtain Tanner /Whitehouse Skinfold Caliper at baseline,3 months- , 1 year-, 2 year- and 3-year follow-up.
Primary measures at 2 years of continuous lifestyle modification.Last measurement at 1 year after last counseling and active treatment has stopped, 3 years from baseline.
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3 years
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Change in self-concept compared to baseline
Periodo de tiempo: 3 years
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Measured with SPPC, Self Perception Profile for Children at baseline, at 6 months- , 1 year-, 2 year- and 3-year follow-up.
Primary outcome measured at 2 years of continuous lifestyle modification.
Last measurement at 1 year after last counseling and active treatment has stopped.
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3 years
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Change in psychiatric health compared to baseline
Periodo de tiempo: 3 years
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Measured with Strengths and difficulties Questionnaire ( SDQ-S)at baseline, at 6 months- , 1 year-, 2 year- and 3-year follow-up.
Primary measurement at 2 years of continuous lifestyle modification.
Last measurement at 1 year after last counseling and active treatment has stopped.
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3 years
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Change in fitness from baseline
Periodo de tiempo: 3 years
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Measured with Andersen's test (shuttle test) at baseline, 1 year-, 2 year- and 3-year follow-up.
Primary measures at 2 years of continuous lifestyle modification.
Last measurement at 1 year after last counseling and active treatment has stopped, 3 years from baseline.
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3 years
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Change in quality of life compared to baseline
Periodo de tiempo: 3 years
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Measured with KINDL (Kinder Lebensqualitet Fragebogen) at baseline, 6 months-, 1 year-, 2 year- and 3-year follow-up.
Primary measures at 2 years of continuous lifestyle modification.
Last measurement at 1 year after last counseling and active treatment has stopped, 3 years from baseline.
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3 years
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Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in lipid levels compared to baseline
Periodo de tiempo: 3 years
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Measurements of total cholesterol, Triglycerides, HDL and LDL at baseline, 1 year-, 2 year- and 3-year follow-up.
Primary measures at 2 years of continuous lifestyle modification.
Last measurement at 1 year after last counseling and active treatment has stopped, 3 years from baseline
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3 years
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Colaboradores
Investigadores
- Silla de estudio: Trond Flægstad, Professor, UNorth Norway
Publicaciones y enlaces útiles
La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.
Publicaciones Generales
- Kokkvoll A, Grimsgaard S, Odegaard R, Flaegstad T, Njolstad I. Single versus multiple-family intervention in childhood overweight--Finnmark Activity School: a randomised trial. Arch Dis Child. 2014 Mar;99(3):225-31. doi: 10.1136/archdischild-2012-303571. Epub 2013 Dec 11.
- Kokkvoll A, Grimsgaard S, Steinsbekk S, Flaegstad T, Njolstad I. Health in overweight children: 2-year follow-up of Finnmark Activity School--a randomised trial. Arch Dis Child. 2015 May;100(5):441-8. doi: 10.1136/archdischild-2014-307107. Epub 2014 Nov 20.
- Kokkvoll AS, Grimsgaard S, Flaegstad T, Andersen LB, Ball GDC, Wilsgaard T, Njolstad I. No additional long-term effect of group vs individual family intervention in the treatment of childhood obesity-A randomised trial. Acta Paediatr. 2020 Jan;109(1):183-192. doi: 10.1111/apa.14916. Epub 2019 Jul 30.
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio
1 de abril de 2009
Finalización primaria (Actual)
1 de diciembre de 2012
Finalización del estudio (Actual)
1 de diciembre de 2013
Fechas de registro del estudio
Enviado por primera vez
30 de marzo de 2009
Primero enviado que cumplió con los criterios de control de calidad
30 de marzo de 2009
Publicado por primera vez (Estimar)
31 de marzo de 2009
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
12 de diciembre de 2014
Última actualización enviada que cumplió con los criterios de control de calidad
11 de diciembre de 2014
Última verificación
1 de diciembre de 2012
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2007/5.2006.3473 (REK)
- 15873 (NSD) (Otro identificador: Norwegian social science data services)
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .