Preschool Based Obesity Prevention Effectiveness Trial
調査の概要
状態
詳細な説明
BACKGROUND:
Obesity is epidemic in the U.S. and is associated with increased risk for numerous medical problems. Many obesity-related risk factors are strikingly apparent in minority populations. Ethnic differences in obesity related risk factors begin as early as six to nine years of age. Thus, the need for overweight prevention efforts as early as the preschool years is critical.
This study builds upon the findings of the "Hip-Hop to Health" program. The primary aim of Hip-Hop was to compare changes in body mass index (BMI [kg/m2]) in two groups of 3- to 5-year-old minority children randomized to a Weight Control Intervention (WCI) or a General Health Control Intervention (GHI). Results for the children at the Year 1 and 2 follow-ups showed that children in the WCI had significantly smaller relative changes in BMI compared to children in the GHI control group. The success was among the schools that served predominantly Black children. Hip-Hop to Health was an efficacy trial delivered by trained specialists in early childhood education, and the first efficacy trial to document change in BMI in preschool children.
DESIGN NARRATIVE:
This study will test a 14-week teacher-delivered weight control intervention (TD-WCI) to a 14-week teacher delivered general health control intervention (TD-GHI) in a randomized community trial occurring in 16 preschools in the Chicago School District. The study has the following aims: 1) to compare children in these two conditions on changes in BMI post intervention and at Year 1 follow-up; 2) to compare children in these two conditions on changes in television viewing, physical activity, and fat, fiber, fruit and vegetable intake at post-intervention and Year 1 follow-up; and 3) to compare classroom teachers in these two conditions on nutrition and exercise knowledge, nutrition attitudes, and support for healthy eating post-intervention and Year 1 follow-up.
The study completion date listed in this record was obtained from the "End Date" entered in the Protocol Registration and Results System (PRS) record.
研究の種類
入学 (予想される)
段階
- 適用できない
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Have received an annual physical
- Parent or guardian willing to give informed consent
- Parent or guardian willing to provide demographic and anthropometric data and agree to complete food intake and physical activity information for their child
Exclusion Criteria:
- Requires a specialized diet outside of that served by the Chicago Public Schools
- Has a chronic physical or behavioral disorder that requires participant to be under close medical psychological supervision and routinely absent from the study
研究計画
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：防止
- 割り当て：ランダム化
- 介入モデル：並列代入
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的：1
Teacher-Delivered Weight Control Intervention
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The teacher-delivered weight control intervention (TD-WCI) is implemented over 14 weeks with three lessons per week.
Many lessons include the use of colorful, friendly, hand-made puppets that represent the seven food groups of the food pyramid (Miss Grain, Miss Fruit, Mr. Vegetable, Mr. Protein, Miss Dairy, Mr. Fat and Miss Sugar).
Please see Appendix IX for complete curriculum and pictures of puppets.
There are three 40-minute lessons per week that consist of a 15-20 minutes interactive healthy eating and exercise didactic session and then 20 minutes of ongoing physical activity (5 minutes warm-up, 15 minutes aerobic activity composed of a number of games and dances with music, 5 minutes cool-down).
In addition to the child-based curriculum the WCI has parent newsletters.
These newsletters are distributed on a weekly basis and provide information that parallels the children's curriculum
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他の：2
Teacher-Delivered General Health Intervention
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The teacher-delivered general health intervention (TD-GHI) serves as the control group in the proposed study.
TD-GHI is a general health intervention that is similar in structure and length to TD-WCI.
Topics include those related to general health and safety, such as car safety, being a good friend, poison safety, disease prevention, etc.
An example of an activity is the 911 emergency call.
The children learn what 911 is and what would be an appropriate call.
They then practice calling 911 on play telephones and relating the important information: nature of the emergency, their name, their address, etc.
They learn also to stay on the phone with the 911 dispatcher until someone comes to help them.
In addition to the child-based curriculum the GHI has parent newsletters.
Like TD-WCI these newsletters are distributed on a weekly basis and provide information that parallels the children's curriculum
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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
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Body height and weight
時間枠：Sept 2006- May 2009
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Sept 2006- May 2009
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Healthy Start Knowledge Quiz
時間枠：Sept 2006- May 2009
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Sept 2006- May 2009
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24-hour diet observation and recall
時間枠：Sept 2006- May 2009
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Sept 2006- May 2009
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Physical activity
時間枠：Sept 2006- May 2009
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Sept 2006- May 2009
|
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Television viewing (child outcomes, measured immediately after the study and at a 1-year follow-up visit)
時間枠：Sept 2006- May 2009
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Sept 2006- May 2009
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Score on short Acculturation Scale (parent outcome, measured immediately after the study and at a 1-year follow-up visit)
時間枠：Sept 2006- May 2009
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Sept 2006- May 2009
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Nutrition and exercise knowledge
時間枠：Sept 2006- May 2009
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Sept 2006- May 2009
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Self-efficacy for eating and exercise behaviors
時間枠：Sept 2006- May 2009
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Sept 2006- May 2009
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Score on Nutrition Attitudes Scale
時間枠：Sept 2006- May 2009
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Sept 2006- May 2009
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Support and role modeling for healthy eating (teacher outcomes, measured immediately after the study and at a 1-year follow-up visit)
時間枠：Sept 2006- May 2009
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Sept 2006- May 2009
|
協力者と研究者
捜査官
- 主任研究者：Marian Fitzgibbon、University of Illinois at Chicago
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
心臓疾患の臨床試験
-
Novartis Pharmaceuticals完了EC-MPS による治療に関心があり、コア研究の 12 か月の治療期間を無事に完了した患者 (de novo Heart Recipients)