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临床试验/NCT07569172
NCT07569172尚未招募不适用

Taabo Enhanced Nutrition and Development Through Economic Rewards

Swiss Tropical & Public Health Institute1 个研究点 分布在 1 个国家目标入组 1,040 人开始时间: 2026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
尚未招募
入组人数
1,040
试验地点
1
主要终点
Prevalence of Complementary Breastfeeding

研究概览

简要总结

The goal of this clinical trial is to learn if a conditional social transfer works to improve rates of complementary breastfeeding. It will also learn about the impacts of social transfers on maternal and child health and development. The main questions it aims to answer are:

  • Does the social transfer increase complementary breastfeeding rates at 24-months postpartum?
  • Does the social transfer increase complementary breastfeeding duration?
  • Does the social transfer impact child health and development?
  • Does the social transfer impact maternal physical and mental health?

Researchers will compare a conditional social transfer to a control group that only receives education about breastfeeding recommendations to see if a conditional social transfers works to increase complementary breastfeeding.

Participants will:

Receive a pamphlet explaining the current recommendations of breastfeeding Receive instructions that if they meet the recommendation to breastfeed until 24-months postpartum they receive a social transfer or receive no additional information Complete home visits at 12- and 24-months postpartum Complete detailed questionnaire

研究设计

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

入排标准

年龄范围
12 Years 至 —(Child, Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Are enrolled in the Taabo multigenerational birth cohort (MGC)
  • Completed the postpartum interview of the Taabo MGC
  • Have a child who is within two weeks of their 12-month birthday,
  • are breastfeeding at time of recruitment,
  • live in the Taabo HDSS, Côte d'Ivoire
  • have no illnesses that contraindicates breastfeeding,
  • had a healthy singleton infant with a birth weight of at least 2500 grams, and
  • agree to participate and sign an informed consent; if underage (12-17 years), a legal representative will also have to agree to sign the informed consent

排除标准

  • Plans to move permanently outside study area
  • Has a medical, intellectual or psychological disability
  • Contraindication for breastfeeding
  • Children born with < 2500 grams

研究组 & 干预措施

Social Transfer

Experimental

A social transfer is provided at the 24-month visit, conditional on the mother still breastfeeding at the time of the visit. They also receive education about current breastfeeding recommendations.

干预措施: Social Transfer (Other)

Control

No Intervention

No intervention is provided besides education on current breastfeeding recommendations.

结局指标

主要结局

Prevalence of Complementary Breastfeeding

时间窗: from 12 to 24 months postpartum

Prevalence of complementary breastfeeding at 24 months postpartum.

Complementary Breastfeeding Duration

时间窗: from 12 to 24 months postpartum

Duration of complementary breastfeeding in weeks.

次要结局

  • CREDI motor z-score(12 months; 24 months)
  • Weight-for-Age z-score(12 months; 24 months)
  • Child Health Outcomes(12 months; 24 months)
  • Percent weight loss(12 months; 24 months;)
  • Mother and Child Hemoglobin Levels(12 months; 24 months)
  • Maternal Depression(12 months; 24 months)
  • Height-for-age z-score(12 months; 24 months)
  • Mid-upper arm circumference (MUAC)(12 months; 24 months)
  • Mother and Child Anemia(12 months; 24 months)
  • Maternal weight change(12 months; 24 months;)
  • Change in systolic and diastolic blood pressure (mmHg)(12 months; 24 months;)
  • Caregiver Reported Early Development Instruments (CREDI) cognitive z-score(12 months; 24 months)
  • CREDI language z-score(12 months; 24 months)
  • CREDI social-emotional z-score(12 months; 24 months)
  • Maternal Anxiety(12 months; 24 months)

研究者

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

Jordyn Wallenborn

Project Leader

Swiss Tropical & Public Health Institute

研究点 (1)

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