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临床试验/NCT02302729
NCT02302729已完成不适用

Professor, Department of Pediatrics, University of Maryland School of Medicine

University of Maryland, Baltimore1 个研究点 分布在 1 个国家目标入组 1,730 人开始时间: 2015年2月16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
1,730
试验地点
1
主要终点
Change in cognitive, motor, social-emotional development from baseline to 12 months

研究概览

简要总结

Over 200 million children under the age of 5 years in low and middle-income countries do not reach their developmental potential, largely due to lack of adequate nutrients and lack of psychosocial stimulation. Stunting (length-for-age < -2 z-scores) is an indication of chronic undernutrition. Guatemala has the high rates of stunting in the Western Hemisphere (over 40%). This trial examines the effect of providing a micronutrient powder manufactured in Guatemala vs. placebo and an early learning environment vs. no early learning environment on the growth, health, and development of young children in Guatemala.

详细描述

The plan is to implement a clustered randomized placebo controlled trial with an infant phase (6-12 months of age) and a preschool phase (36-48 months of age). For the infant phase, the investigators will use ProPAN (Process for the Promotion of Child Feeding) in the development of the evaluation and intervention, with modifications as necessary for the Guatemalan context. ProPAN is a tool developed and distributed by the Pan American Health Organization to develop, implement, and evaluate interventions and programs to improve infant and young child diet and feeding. ProPAN includes four modules:

Module 1: Assessment Module 2: Testing Recipes and Recommendations Module 3: Intervention Module 4: Monitoring and Evaluation

For the preschool phase, the investigators will use an evidence-based school readiness intervention (Little By Little) that has been shown to be effective with Hispanic preschoolers. The intervention will be implemented through the Association for the Prevention and Study of HIV/AIDS who will train and supervise the community health workers. By working directly with a local non-profit organization, the project will be well positioned to inform strategies to scale up the intervention on a community wide basis, if beneficial effects are shown.

The project examines the effects of an integrated intervention that includes both micronutrient powder added to food and responsive feeding for infants or school readiness for preschoolers. The primary aim is to examine how an integrated micronutrients + responsive feeding/school readiness intervention changes the development (primary outcome), growth and micronutrient status (secondary outcomes) of young children. The investigators will focus on infants (6-12 months) when the risk for micronutrient deficiencies is high, as they transition from breast feeding to complementary feeding and the family diet. The investigators will focus on preschoolers (36-48 months) to examine if micronutrients + a school readiness intervention can improve children's school readiness skills. The design includes neighborhood clusters randomized into four groups: 1) micronutrients plus responsive feeding/school readiness 2) micronutrients only, 3) placebo plus responsive feeding/school readiness, and 4) placebo only.

The investigators will test the following hypotheses:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
6 Months 至 4 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Child speaks Spanish.
  • Child is age 6-12 months or age 36-48 months.
  • Child must be undernourished (length and height for age < -1 z-score).
  • Child does not have any obvious health or developmental problems that would interfere with growth, nutrition, or development.
  • Child will remain in the area for the subsequent year.
  • Parent or legal guardian of the child is age 18 years or older.
  • Parent or legal guardian speaks and understands Spanish.
  • Parent or legal guardian lives with child in study community.

排除标准

  • Child is not age 6-12 months or 36-48 months.
  • Child has severe stunting (length and height for age < -3 z-scores).
  • Child has identified conditions that could interfere with their development and growth.
  • Child is severely anemic (hemoglobin < 7).

研究组 & 干预措施

Placebo and No responsive caregiving

Placebo Comparator

Placebo and No responsive caregiving

干预措施: Placebo (Dietary Supplement)

Micronutrients No responsive feeding

Experimental

Micronutrient powder and no responsive feeding

干预措施: Micronutrients (Dietary Supplement)

Placebo and Responsive Feeding

Placebo Comparator

Placebo (vitamin B2) and Responsive Feeding

干预措施: Responsive feeding (Behavioral)

Placebo and Responsive Feeding

Placebo Comparator

Placebo (vitamin B2) and Responsive Feeding

干预措施: Placebo (Dietary Supplement)

Micronutrients and Responsive caregiving

Experimental

Micronutrients and Responsive feeding intervention

干预措施: Micronutrients (Dietary Supplement)

Micronutrients and Responsive caregiving

Experimental

Micronutrients and Responsive feeding intervention

干预措施: Responsive feeding (Behavioral)

结局指标

主要结局

Change in cognitive, motor, social-emotional development from baseline to 12 months

时间窗: Baseline, 12 months

Cognitive and social-emotional assessments

次要结局

  • Change in micronutrient status from baseline to 12 months(Baseline, 12 months)
  • Change in Growth from baseline to 12 months(Baseline, 12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Maureen Black

Professor

University of Maryland, Baltimore

研究点 (1)

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