- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01018121
Behavioral Rx & Nutrition in Pediatric Chronic Disease (LAUNCH)
LAUNCH II: Learning About Activity and Understanding Nutrition for Better Child Health
The objective of this project is to pilot test a behavioral intervention for modifying the diet and physical activity patterns of overweight preschool children through improved parenting and nutritional education(LAUNCH). This intervention will be compared to standard of care for preschool overweight in the primary care setting using a randomized clinical trial design (RCT. The results of this pilot RCT will provide data integral to estimating the effect size for a more definitive RCT of the intervention in the future. The primary hypothesis is:
H1: LAUNCH will result in a significantly greater decrease in BMI z score compared to the standard of care at 12 months post-treatment.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 2
- Fase 1
Kontakter og lokationer
Studiesteder
-
-
Ohio
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Cincinnati, Ohio, Forenede Stater, 45229
- Cincinnati Children's Hospital Medical Center
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- child age between 2- 5 years;
- child > 95th percentile BMI for age and sex 12, but not more than 100% above the mean BMI;
- medical clearance from pediatrician; and
- at least one parent with a BMI > 25. -
Exclusion Criteria:
- non-English speaking;
- living more than 50 miles from the medical center;
- a disability/illness that would preclude engagement in at least moderate physical activity;
- medical condition/medication associated with weight gain; or 5) enrolled in another weight control program.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: Clinic and Home Behavioral Intervention
|
A 6-month intervention consisting of two phases: Phase I (Intensive Intervention), 12 weekly sessions that alternated between group-based clinic sessions (parent and child concurrent groups) and individual home visits and Phase II (Maintenance), 12 weeks of every other week sessions, alternating between group sessions in-clinic and home sessions.
Targeted 3 components: 1) Dietary education with age-specific caloric targets, healthy eating recommendations for children following the AAP guidelines used in the PC session; 2) Physical Activity education with age-specific activities for children and families; and 3) Parenting skills to achieve the diet and physical activity goals using behavioral management skills and parent modeling of eating and activity.
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Aktiv komparator: Pediatrician Counseling
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A one time 45-minute visit with a board certified pediatrician for each family that focused on the AAP guidelines for eating and physical activity for children
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
BMI z score
Tidsramme: Baseline, 6 months, 12 months
|
Baseline, 6 months, 12 months
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
Parent weight loss
Tidsramme: baseline, 24 weeks, 48 weeks
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baseline, 24 weeks, 48 weeks
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Child caloric intake
Tidsramme: baseline, 6 months, 12 months
|
baseline, 6 months, 12 months
|
Home food and activity environment
Tidsramme: baseline, 6 months, 12 months
|
baseline, 6 months, 12 months
|
Child physical activity
Tidsramme: baseline, 6 motnhs, 12 months
|
baseline, 6 motnhs, 12 months
|
Parent-child mealtime interactions
Tidsramme: baseline, 6 months, 12 months
|
baseline, 6 months, 12 months
|
Samarbejdspartnere og efterforskere
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Lori J Stark, Ph.D., Children's Hospital Medical Center, Cincinnati
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 103254
- K24DK059492 (U.S. NIH-bevilling/kontrakt)
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