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The Effect of Mother Touch on High-Risk Newborns and Mothers

The Effect of Mother Touch on High-Risk Newborns and Mothers

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0010573
Enrollment
50
Registered
2025-06-01
Start date
2024-12-24
Completion date
Unknown
Last updated
2025-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Others(Mother Touch) : Mother Touch = Mother's Touch a total of six hospital stays three times a week / about two weeks Through a 20-minute program in which the mother gives high-risk newborns touch t

Sponsors

Eulji University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) a high-risk newborn ? A high-risk newborn with stable vital signs under the judgment of the medical staff ? a high-risk newborn with no symptoms of infection (2) a mother of a high-risk newborn ? Mother who understood the purpose of the study and agreed to participate in this study ? Mother who can understand and write the contents of the survey ? A mother whose child has never been admitted to a neonatal intensive care unit in the past

Exclusion criteria

Exclusion criteria: (1) a high-risk newborn ? High-risk newborns admitted to neonatal intensive care units for less than two weeks ? a high-risk newborn with a birth defect ? High-risk newborns with skin disorders and infectious diseases (2) a mother of a high-risk newborn ? Mothers in need of treatment as postpartum complications limit her daily life ? a mother who doesn't want to breastfeed ? a mother who is subject to drug-induced breastfeeding

Design outcomes

Primary

MeasureTime frame
the amount of feeding;Growth;Physiological reaction;Behavioral State;Mother-Child Attachment

Secondary

MeasureTime frame
Postpartum Depression

Countries

Korea, Republic of

Contacts

Public ContactHEEJEE JO

Eulji University Uijeongbu Campus

yellowmint@naver.com+82-31-951-3816

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026