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The Effect of Lullaby During Bath Time on Mother-Infant Bonding, Postpartum Depression, and Parental Self-Efficacy in Infants

I

Istanbul University - Cerrahpasa

Status

Begins enrollment in 3 months

Conditions

Self Efficacy
Bonding
Postpartum Depression (PPD)
Newborn Infant

Treatments

Behavioral: Maternal Lullaby Singing

Study type

Interventional

Funder types

Other

Identifiers

NCT07370025
2025/728

Details and patient eligibility

About

This randomized, single-blind controlled trial aims to evaluate the effects of maternal lullaby singing during infant bathing on mother-infant bonding, postpartum depressive symptoms, and perceived parenting self-efficacy in mothers of healthy term infants. The postpartum period represents a critical phase for maternal psychological adjustment, during which stress, depressive symptoms, and low parenting confidence may negatively affect the quality of mother-infant interaction and bonding. Low-cost, culturally meaningful, and non-pharmacological interventions that support maternal well-being and early bonding are therefore of particular importance.

The study will be conducted with mothers who have delivered healthy term infants in a public hospital. Eligible participants will be randomly assigned to either an intervention group or a control group. Mothers in the intervention group will receive a structured bathing education and will be instructed to bathe their infants three times per week for two consecutive weeks while singing a lullaby using their own voice in a calm and quiet home environment. Live-recorded music will not be used. The intervention emphasizes sensory interaction, emotional closeness, and maternal voice as key components. Each bathing session is expected to last approximately 10-15 minutes. The control group will receive routine postpartum care without a structured lullaby-based bathing intervention.

Outcome measures include mother-infant bonding, postpartum depressive symptoms, and perceived maternal parenting self-efficacy. Data will be collected at two time points: prior to hospital discharge (within the first 24 hours postpartum) and at the end of the two-week intervention period. Validated self-report instruments will be used for all outcome assessments.

The findings of this study are expected to provide evidence on the effectiveness of a simple, culturally embedded caregiving practice in supporting maternal mental health, strengthening mother-infant bonding, and enhancing parenting confidence during the early postpartum period. Results may inform postpartum care practices, parental counseling programs, and midwife-led supportive interventions.

Enrollment

98 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Mothers who have had an uncomplicated pregnancy and delivery
  • Mothers who are healthy enough to care for their baby
  • Mothers who have suitable conditions at home to bathe their baby
  • Babies born at term (≥ 37 weeks of gestation) and with stable general health after birth

Exclusion criteria

  • Mothers with a history of serious postpartum complications (such as postpartum hemorrhage)
  • Mothers diagnosed with psychiatric illness
  • Mothers who are unable to participate directly in the care of their baby (due to severe disability, mandatory bed rest, etc.)
  • Mothers who cannot participate in the lullaby program due to hearing impairment
  • Infants who experience serious respiratory, cardiac, or neurological problems at birth or thereafter, who have a skin disease or dermatological condition that limits bathing, who have a history of admission to the neonatal intensive care unit, or who have a chronic disease or congenital anomaly

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

98 participants in 2 patient groups

Lullaby Group
Experimental group
Treatment:
Behavioral: Maternal Lullaby Singing
Control Group
No Intervention group

Trial contacts and locations

1

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Central trial contact

Elif DOGAN

Data sourced from clinicaltrials.gov

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