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Impact of the Korea Early Childhood Home-visiting Intervention (KECHI)

Seoul National University logo

Seoul National University

Status

Active, not recruiting

Conditions

Maternal Distress
Child Development
Parenting
Pregnancy Related
Infant Development

Treatments

Behavioral: Targeted nurse-led home visiting

Study type

Interventional

Funder types

Other

Identifiers

NCT04749888
KCT0005579 (Registry Identifier)
RS-2025-00516414 (Other Grant/Funding Number)
C-1911-150-1083
HI19C0481, HC19C0048 (Other Grant/Funding Number)

Details and patient eligibility

About

Maternal and early childhood home visits have been proposed as an effective strategy to improve the health and development of disadvantaged children. In South Korea (hereafter, Korea), a maternal and early childhood home visit program has been implemented since 2013 in Seoul, and then was adopted in 2019 by the central government as a national policy for child health and development.

The Korea Early Childhood Home-visiting Intervention (KECHI) encompasses 25-29 home visits, group activities, and community service linkage by social workers from the prenatal period until the child reaches the age of 2 years; as such, it is a complex intervention involving various domains to address a wide range of outcomes. Each home visit is implemented based on the family's needs, and individualized interventions are provided to improve parenting and the home environment in order to promote children's health and development and maternal health.

This study is a randomized controlled community trial conducted in Korea to examine the impact of targeted home visits led by nurses in the prenatal and early childhood period on children's health and development and maternal health.

This study is a superiority trial with two parallel groups from pregnancy until the child reaches 2 years of age. Pregnant women with two or more risk factors will be recruited to participate in the study after they provide informed consent. Participants will then be randomly assigned to the intervention or control group with a 1:1 allocation through an independent web-based random allocation system. We expect a total of 800 families (400 families in each group) to be recruited. The intervention group will receive the KECHI program and the control group will receive existing maternal and child health services (usual care), but not multiple home visits by nurses. Both groups will receive gift cards of 30,000 Korean won (about 27 USD) for each round of surveys.

The intervention and control groups will be surveyed on the outcome variables of home environment, child development, breastfeeding, maternal health, child hospital visits due to injuries, and community service linkage at four home visits by trained research nurses at baseline and at 6 months, 12 months, and 24 months after birth. Telephone contact will also be made at 6 weeks and 18 months after birth for both groups. Outcome measurements will be performed by research nurses and data management will be conducted by statistical analysts. The analysis will be conducted for the intention-to-treat (ITT) and per-protocol (PP) groups, with an interim analysis of outcomes up to the 6-month follow-up. For the primary outcomes and certain secondary outcomes, subgroup analyses will be performed based on factors such as region, fertility status, number of risk factors, presence of depression, education level, etc. Furthermore, this study will utilize administrative data available for all study participants to evaluate both short and long-term impacts of the KECHI intervention on maternal and child outcomes.

Enrollment

800 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Pregnant women with two or more risk factors at the time of screening
  • Pregnant women at less than 37 weeks of gestation
  • Pregnant women who can read and answer questionnaires in Korean

Exclusion criteria

  • Pregnant women who have experienced any critical event such as termination of pregnancy, stillbirth, or child death
  • Pregnant women who plan to move abroad or to other regions where the KECHI service is not available within the next 6 months

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

800 participants in 2 patient groups

Targeted nurse-led home visiting
Experimental group
Description:
The intervention group will receive 25-29 home visits during pregnancy and the first 2 years of life conducted by child health nurses. The frequency of home visits will be determined by nurses based on the needs of the families. The content of each home visit is individually tailored to the mother's needs, skills, strengths, and capacity using parenting education materials.
Treatment:
Behavioral: Targeted nurse-led home visiting
Control group
No Intervention group
Description:
The control group will receive existing maternal and child health services (usual care) except for the targeted nurse-led home visits.

Trial contacts and locations

2

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Central trial contact

Yu-Mi Kim, MD, PhD; Young-Ho Khang, MD, PhD

Data sourced from clinicaltrials.gov

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