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Can involving partners in breastfeeding counselling help first-time mothers breastfeed exclusively for six months?

Partner-inclusive postpartum counselling versus breastfeeding friendly hospital initiative (BFHI) standard care to improve six-month exclusive breastfeeding among primiparous women

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN54832662
Enrollment
214
Registered
2026-06-26
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Improving exclusive breastfeeding at six months among primiparous postpartum women. Pregnancy and Childbirth

Interventions

This is a two-arm, parallel-group randomized controlled trial. Eligible primiparous postpartum women and their partners will be randomly allocated in a 1:1 ratio to either the intervention or control

Sponsors

University Malaya Medical Centre
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Primiparous women aged 18 years or older 2. Delivered a healthy singleton term infant (=37 completed weeks' gestation) 3. Intend to exclusively breastfeed their infant 4. Recruited within 24–48 hours postpartum prior to hospital discharge 5. Able to understand the study information and provide written informed consent 6. Have a partner who is available, willing to participate in the counselling session and follow-up assessments, and able to provide written informed consent

Exclusion criteria

Exclusion criteria: 1. Mothers with medical contraindications to breastfeeding 2. Infants requiring prolonged neonatal intensive care unit (NICU) admission or with significant medical conditions that preclude breastfeeding 3. Mothers or partners unable to understand the study information or communicate in the study languages 4. Mothers or partners with major psychiatric illness, cognitive impairment, or any condition that would limit participation or informed consent 5. Women who screen positive for intimate partner violence (IPV) using the HARK screening tool 6. Partners who are unavailable or unwilling to participate in the counselling session and follow-up assessments

Design outcomes

Primary

MeasureTime frame
Exclusive breastfeeding at six months postpartum measured using the WHO 24-hour infant feeding recall method at 6 months postpartum

Secondary

MeasureTime frame
Maternal breastfeeding self-efficacy measured using the Breastfeeding Self-Efficacy Scale–Short Form (BSES-SF) at baseline, 3 months postpartum, 6 months postpartum;Partner breastfeeding attitudes measured using the Iowa Infant Feeding Attitude Scale for Partners (IIFAS-P) at baseline, 3 months postpartum, 6 months postpartum

Countries

Malaysia

Contacts

Public ContactChieng Han Ling
lingchienghan@ummc.edu.my+60 03-79494422

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Jul 23, 2026