- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT00528164
Team PLAY (Positive Lifestyles for Active Youngsters) (Team PLAY)
15 februari 2013 uppdaterad av: University of Tennessee
Treating Childhood Obesity With Family Lifestyle Change
The purpose of this study is to determine whether an intense family-centered program to help children, 4 to 7 years old, control their weight is more effective than the advise and referrals their health provider gives in the primary care office.
Studieöversikt
Detaljerad beskrivning
This randomized controlled trial is designed to determine whether an intense 6 month family-centered intervention to increase physical activity and health eating patterns, primarily directed at parents, followed by a 6 month maintenance period, will be significantly more successful in controlling weight in overweight/obese children, ages 4-7 years, than usual standard care, at 2 years after enrollment.
The intervention group (180 children with a BMI > 85% percentile) will receive standard of care, as well as, additional parental counseling.
Parents will receive intense counseling regarding developmentally appropriate physical activity, strategies for reducing sedentary behaviors, nutritional counseling, and behavioral counseling including a self-management program to use with their children at home.
The group will meet once a week for the initial 8 weeks, biweekly for 8 weeks, and monthly for 2 months.
Following this period (the next 6 months), a case manager will call the family on a monthly basis and the family will be sent educational and support information by mail.
The control group (60 children with a BMI > 85% percentile) will receive standard care provided by their primary care provider and be offered a six week optional parenting class.
All children will have a medical history, physical examination, and anthropometric measures, nutritional assessment, measurement of physical activity, and behavioral/psycho-social measures provided by study personnel.
Outcome measurements will be done at baseline, 6, 12, 18, and 24 months.
Studietyp
Interventionell
Inskrivning (Faktisk)
270
Fas
- Fas 2
- Fas 3
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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Tennessee
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Memphis, Tennessee, Förenta staterna, 38105
- University of Tennessee, Department of Preventive Medicine
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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
4 år till 7 år (Barn)
Tar emot friska volontärer
Ja
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Children 4 to 7 years of age, male or female, of any race who have a BMI > 85% for age.
- All participants and parents must be able to speak and understand English.
Exclusion Criteria:
- History of diabetes mellitus
- History of significant renal, hepatic, cardiovascular,or gastrointestinal disease
- Receiving drugs known to alter glucose homeostasis
- Physical disabilities that limit physical activity (i.e. orthopedic, congenital)
- Diagnosis of hypertension by a medical provider that requires limited physical activity
- Psychological disabilities that might limit participation;
- Lack of access to a telephone
- Lack of access to transportation for the intervention
- Current participation in another clinical trial (current participation in an observational study is not an exclusion.)
- Other medical or behavioral factors that in the judgment of the Principal Investigator may interfere with study participation or the ability to follow the intervention protocol.
- Unable to speak and understand English
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: Team PLAY Group
6-month family-centered intervention to increase physical activity and healthy eating patterns, primarily directed at parents.
Parents will receive intense counseling regarding developmentally appropriate physical activity, strategies for reducing sedentary behaviors, nutritional counseling, and behavioral counseling, including a self-management program to use with their children at home.
The group will meet once a week for the initial 8 weeks, bi-weekly for 8 weeks, and monthly for 2 months.
|
Parents will receive intense counseling regarding developmentally appropriate physical activity, strategies for reducing sedentary behaviors, nutritional counseling, and behavioral counseling, including a self-management program to use with their children at home.
The group will meet once a week for the initial 8 weeks, bi-weekly for 8 weeks, and monthly for 2 months.
|
|
Inget ingripande: Standard Care Group
Participants receive standard care by primary care physician.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
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Primary - Body Mass index
Tidsram: 2 years
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2 years
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Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
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Body Composition (DXA), physical activity (accelerometry), dietary changes (Block Food Frequency), Flexibility and Cohesion Evaluation Scales, MacArthur Behavior and Health Questionnaire and Body Esteem Scale.
Tidsram: 2 years
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2 years
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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Samarbetspartners
Utredare
- Huvudutredare: Marion E Hare, MD,MS, University of Tennessee
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
- Williams NA, Fournier J, Coday M, Richey PA, Tylavsky FA, Hare ME. Body esteem, peer difficulties and perceptions of physical health in overweight and obese urban children aged 5 to 7 years. Child Care Health Dev. 2013 Nov;39(6):825-34. doi: 10.1111/j.1365-2214.2012.01401.x. Epub 2012 Aug 8.
- Hare ME, Coday M, Williams NA, Richey PA, Tylavsky FA, Bush AJ. Methods and baseline characteristics of a randomized trial treating early childhood obesity: the Positive Lifestyles for Active Youngsters (Team PLAY) trial. Contemp Clin Trials. 2012 May;33(3):534-49. doi: 10.1016/j.cct.2012.02.003. Epub 2012 Feb 10.
- Williams NA, Coday M, Somes G, Tylavsky FA, Richey PA, Hare M. Risk factors for poor attendance in a family-based pediatric obesity intervention program for young children. J Dev Behav Pediatr. 2010 Nov-Dec;31(9):705-12. doi: 10.1097/DBP.0b013e3181f17b1c.
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 september 2006
Primärt slutförande (Faktisk)
1 juni 2012
Avslutad studie (Faktisk)
1 juni 2012
Studieregistreringsdatum
Först inskickad
11 september 2007
Först inskickad som uppfyllde QC-kriterierna
11 september 2007
Första postat (Uppskatta)
12 september 2007
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
18 februari 2013
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
15 februari 2013
Senast verifierad
1 februari 2013
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 1RO1HDO50895-01
- USPHS Gr HD-050895-01
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 .