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临床试验/NCT05595161
NCT05595161已完成不适用

Dissemination and Implementation of the Bright Bodies Intervention for Childhood Obesity

Yale University6 个研究点 分布在 1 个国家目标入组 184 人开始时间: 2022年10月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
184
试验地点
6
主要终点
Change in %BMIp95

研究概览

简要总结

This study will evaluate the effectiveness of the Bright Bodies intervention in improving body mass index (BMI) among 7-13 year-old children with obesity simultaneously with the impact of the implementation strategy on adoption, reach, fidelity, cost, and maintenance of the intervention in three heterogenous settings serving patients disproportionately affected by obesity.

详细描述

The demonstrated efficacy of Bright Bodies in a well-designed randomized controlled trial (RCT) and a real-world effectiveness study reduce equipoise and challenge the ethics of a prospective RCT of implementing Bright Bodies in other settings. As such, this study is an observational, multiphase mixed methods design to evaluate effectiveness and implementation among three purposively selected heterogeneous sites serving low-income populations with racial and ethnic, rural-urban, and geographic diversity.

Children ages 7-13 years with BMI ≥85th percentile and their parent/caregivers hereafter referred to as parent will be recruited to participate in the evaluation study from among participants in the newly-established Bright Bodies programs at each of the three implementation sites. The aim is for each site to recruit approximately 40 children and their parents (a total of 120 children and 120 parents) to participate in the Bright Bodies program over the study's enrollment period. The primary outcome is change in BMI expressed as a percentage of the 95th percentile (%BMIp95) using EHR data collected as part of routine clinical care up to 36 months before and up to 15 months after enrollment in the intervention. Secondary outcomes include: (a) change in %BMIp95 at three and six months, (b) changes in parent BMI at three and six months, (d) parent-reported changes in health behaviors (sleep, physical activity, screen time, eating behaviors), via surveys at 3, 6 and 12 months, and (e) changes in parent-proxy reported weight-related quality of life, parent stress, and parent talk about weight via surveys at baseline, 6, and 12 months after enrollment. We will also describe implementation outcomes (reach, adoption, fidelity/adaptation, and cost) through qualitative and quantitative data collection from members of our study team throughout the process of implementation.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
7 Years 至 13 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children ages 7-13 years with BMI ≥85th percentile and their parents;
  • Child-parent dyads enrolled in the Bright Bodies intervention at each site will be eligible for inclusion in the evaluation study.

排除标准

  • Children and/or parents who do not speak the language in which the program will be delivered at each site;
  • Children and/or parents who plan to move away from the area within the next 15 months;
  • Children with a history of purging and/or dramatic weight loss prior to the trial;
  • Children who are currently participating in another high-intensity lifestyle intervention or other similar research study, or are planning to have bariatric surgery within the next six months
  • Children whose EHR data cannot be accessed by the study teams;
  • Children with chronic medical conditions limiting their ability to take food by mouth (e.g., g-tube fed, total parenteral nutrition), participate in physical activity (e.g., wheelchair bound), or meaningfully participate in group sessions (e.g., cognitive impairment);
  • Children with a sibling enrolled in the trial
  • Children who join the Bright Bodies program after the 4th week of a session (not including orientation)

研究组 & 干预措施

Intervention

Experimental

Bright Bodies

干预措施: Bright Bodies (Behavioral)

结局指标

主要结局

Change in %BMIp95

时间窗: Up to 36 months prior to baseline through up to 15 months after enrollment

Change in %BMIp95, calculated from height and weight. A negative percentage indicates that the participant's BMI has decreased since enrollment.

次要结局

  • Change in parent BMI(Baseline through 6 months after enrollment)
  • Change in weight-related quality of life(Baseline through 12 months after enrollment)
  • Change in weight-related health behaviors.(Baseline through 12 months after enrollment)
  • Change in binge eating behaviors.(Baseline through 12 months after enrollment)
  • Change in parent conversations about weight.(Baseline through 12 months after enrollment)
  • Per patient cost for participation in Bright Bodies(From enrollment through 12 months after enrollment)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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