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临床试验/NCT02458833
NCT02458833已完成不适用

Home Plate: A Randomized Controlled Trial of a Community-Engaged Intervention to Improve Home Food Preparation Practices and Health During Early Childhood

Children's Hospital of Philadelphia1 个研究点 分布在 1 个国家目标入组 115 人开始时间: 2015年6月1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
115
试验地点
1
主要终点
Dietary Energy Density (Child Participants)

研究概览

简要总结

This study aims to test the effectiveness of a community-based, peer-mentored intervention to improve home food preparation practices in families with young children.

详细描述

Barriers to healthy eating and active living are at the heart of the obesity epidemic. This study focuses on a key factor underlying healthy eating: home food preparation. This study aims to test the effectiveness of a community-based, peer-mentored intervention to improve home food preparation practices in families with young children. The investigators will partner with community-based organizations serving families with children ages 1 to 3 years in West Philadelphia aiming specifically to:

  1. Test the intervention's effect on diet and physical health.

Hypothesis 1: The intervention group will have improved home food preparation practices and a healthier diet compared to the control group. 2. Test the intervention's effect on family health.

Hypothesis 2: The intervention group will report improved parenting skills and more hopeful patterns of thinking. 3. Identify factors present at baseline and during engagement with the intervention that distinguish intervention participants who have improved diet, physical health, and family health from those who do not.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •English-speaking
  • •Able to give informed consent.
  • •Legal guardian and caregiver of at least one child, age 1-3 years
  • •Inclusion Criteria: children
  • •1-3 year old children of mentee primary caregivers enrolled in the study
  • •If a mentee caregiver has more than one child, then all their eligible children (ages 1-3 years) will be enrolled in the study.
  • •Inclusion Criteria: peer mentors
  • •Eligible peer mentors should meet the inclusion criteria set forth above for mentees. (Children of peer mentors will not be eligible for this study.)
  • •In addition,
  • •The study team will decide which participants will be invited to be peer mentors, based on attributes including interest, leadership ability, and home food preparation skills.

排除标准

  • •Caregivers and children not meeting the inclusion criteria above.
  • •Caregivers who are pregnant at the time of enrollment.
  • •Caregivers or children with a medical condition that significantly affects their diet or eating habits. (The study team will ask during the time of recruitment if subjects or their children have a medical condition that significantly affects diet or eating habits.)
  • •Subjects who, in the opinion of the Investigator, may be unable to participate in the study schedules or procedures.

研究组 & 干预措施

Intervention

Experimental

Behavioral: Home Plate intervention

干预措施: Home Plate (Behavioral)

Delayed Entry Control

Experimental

This Arm will receive the Home Plate intervention 3 months after the Intervention Arm completes the intervention.

干预措施: Home Plate (Behavioral)

结局指标

主要结局

Dietary Energy Density (Child Participants)

时间窗: 19-30 weeks from baseline

Child participants' 24-hour dietary recalls will be collected by trained study staff from adult caregivers. 24-hour dietary recalls will be collected on a minimum of 2 and a maximum of 3 separate days. The results will then be used to calculate the energy density of the child's diet.

次要结局

  • Emotional and Family Health(19-30 weeks from baseline)
  • Home Food Environment(19-30 weeks from baseline)
  • Diet Quality(19-30 weeks from baseline)
  • Home Food Preparation Practices(19-30 weeks from baseline)
  • Household Routines(19-30 weeks from baseline)
  • Body mass index(19-30 weeks from baseline)
  • Dietary Energy Density (Adult Participants)(19-30 weeks from baseline)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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