- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT00872807
The Activity School in Finnmark for Overweight Children
11 december 2014 uppdaterad av: 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.
Studieöversikt
Status
Avslutad
Intervention / Behandling
Detaljerad beskrivning
Randomized study design with two parallel groups.Active intervention in two years, last follow-up after 3 years.
Studietyp
Interventionell
Inskrivning (Faktisk)
97
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Hammerfest, Norge, 9600
- Childrens departement Finnmark Hospital, Norway
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
6 år till 12 år (Barn)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
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.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: 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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Aktiv komparator: 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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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Change in Body Mass Index compared to baseline
Tidsram: 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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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Change in Systolic Blood Pressure compared to baseline
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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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Andra resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Change in lipid levels compared to baseline
Tidsram: 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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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Samarbetspartners
Utredare
- Studiestol: Trond Flægstad, Professor, UNorth Norway
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Allmänna publikationer
- 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.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 april 2009
Primärt slutförande (Faktisk)
1 december 2012
Avslutad studie (Faktisk)
1 december 2013
Studieregistreringsdatum
Först inskickad
30 mars 2009
Först inskickad som uppfyllde QC-kriterierna
30 mars 2009
Första postat (Uppskatta)
31 mars 2009
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
12 december 2014
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
11 december 2014
Senast verifierad
1 december 2012
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 2007/5.2006.3473 (REK)
- 15873 (NSD) (Annan identifierare: Norwegian social science data services)
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .