- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01515254
The Feeding Dynamic Intervention: Self Regulation of Intake in Preschoolers (FeeDIn)
The Feeding Dynamic Intervention Study
연구 개요
상세 설명
Childhood obesity is a significant public health problem. In the last three decade, there has been a marked increase in the prevalence of childhood obesity. Currently, 23% of preschoolers (2-5 years) in the United States are overweight or obese, a critical period to target in hopes of reversing this trend. The purpose of this study is to test the efficacy of a novel obesity intervention program for preschool-aged children. Emerging consensus indicates that excessive, intrusive, overt control in feeding or a chaotic non-structured feeding environment are risk factors for childhood obesity. The 2007 Expert Committee Recommendations on the Prevention, Assessment, and Treatment of Childhood Obesity specifically identified maternal feeding practices as important, categorically stating there is consistent evidence to support "avoiding overly restrictive feeding behaviors." The guidelines emerged from a growing body of literature indicating that overly controlling caregiver feeding behaviors, in particular, significantly increase children's obesity risk.
Despite the evidence for the importance of feeding dynamics, no childhood obesity interventions focused on this area have been rigorously tested. The Feeding Dynamic Intervention (FDI) is a 12-week educational intervention. The intervention will be delivered in a closed group setting and will consist of 6 intervention sessions lasting 90 minutes each. We will recruit 84 mothers with 3- to 5-year-old obese children, randomly assigned to either the FDI or a comparison to a waiting list control group (WLG). At the end of the 6 month study we will assess knowledge and behavioral changes between the groups on (i) maternal self-reported feeding practices; (ii) improving energy compensation (COMPX), decreasing Eating in the Absence of Hunger (EAH) and increasing mother-reported satiety responsiveness in their child. Finally, we will investigate an exploratory hypothesis that children in the FDI group, compared to children in the wait-list control group, will demonstrate a lower increase in body mass index (BMI) z-score over 6 months.
연구 유형
등록 (실제)
단계
- 해당 없음
연락처 및 위치
연구 장소
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Ohio
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Columbus, Ohio, 미국, 43205
- Nationwide Children's Hospital
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- The child is between ages 3-5 years (36 to 71 months). [Note if a family has more than one qualifying child we will choose the child with the lower CEBQ SR score and if they are equal we will randomly select the target child for the study dyad.]
- Child's body mass index > 85th percentile for age and sex
- This will be calculated based on age, weight and height using the Center for Healthy Weight and Nutrition BMI calculator [if mother is unsure of the weight and height ask whether she has been told her child is overweight or obese by the PCP]
- Child has significantly abnormal parent-reported impairment of energy regulation (Rating of 2.8 or lower on the CEB-Q).
- The mother is fluent in English (measures are limited to English at this time)
- Mother (or female caregiver) has primary legal and physical custody of the child and is primarily responsible for feeding the child. Specifically the child is not in a non-parental home daycare more than 20 hours/week. Structured child care centers are not included in this limitation because they use structure care and feeding techniques similar to those taught in the FeeDIn Program.
Exclusion Criteria:
- Child has a medical condition or takes a medication that affects appetite, eating, or growth;
- Child has food allergies or dietary restrictions that interfere with feeding or the study tests (i.e., milk, gluten and eggs?)
- Child has any developmental or behavioral diagnosis that might affect his/her ability to respond to a behaviorally-based intervention, e.g., cognitive impairment, language delay, or autism.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 하나의
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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간섭 없음: No intervention- control group
Visits to physicians, WIC offices, nutrition program etc will be tracked.
The subjects will undergo the energy regulation tests at baseline and 3 months.
They will complete surveys and have their weight taken.
The control group subjects will have the opportunity to receive the intervention at the end of the study
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|
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실험적: lifestyle counseling, parental feeding
Intervention group subjects will undergo a Feeding Dynamic Intervention (FDI).
The intervention will be delivered in a closed group setting and will consist of 6 intervention sessions lasting 90 minutes each.
Visits to physicians, WIC offices, nutrition program etc will be tracked.
The subjects will undergo the energy regulation tests at baseline and 3 months.
They will complete surveys and have their weight taken.
|
Intervention group subjects will undergo a Feeding Dynamic Intervention (FDI).
The intervention will be delivered in a closed group setting and will consist of 6 intervention sessions lasting 90 minutes each.
Visits to physicians, WIC offices, nutrition program etc will be tracked.
The subjects will undergo the energy regulation tests at baseline and 3 months.
They will complete surveys and have their weight taken.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Increased Energy Regulation
기간: Change from baseline in energy compensation at 3 months and Change from baseline in energy compensation at 6 months
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Children in the FDI group, compared to children in the wait-list control group will show improved energy compensation regulation (COMPX), decreased Eating in the Absence of Hunger (EAH), and increasing Satiety Responsiveness (CEBQ-SR).
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Change from baseline in energy compensation at 3 months and Change from baseline in energy compensation at 6 months
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Reduce BMI
기간: Change from baseline in BMI-z score at 3 months and Change from baseline in BMI-z score at 6 months
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Children in the FDI group, compared to children in the wait-list control group, will demonstrate a lower increase in body mass index (BMI) z-score over 6 months.
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Change from baseline in BMI-z score at 3 months and Change from baseline in BMI-z score at 6 months
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공동 작업자 및 조사자
수사관
- 수석 연구원: Ihuoma Eneli, MD, MS, Nationwide Children's Hospital
간행물 및 유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .