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LatchOn: a breastfeeding support study

LatchOn: a protocol for a multi-centre, randomised controlled trial of perinatal support to improve breastfeeding outcomes in women with overweight and obesity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14819650
Enrollment
220
Registered
2019-02-11
Start date
2019-05-01
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Breastfeeding Pregnancy and Childbirth

Interventions

Current interventions as of 03/09/2021: Randomisation will be 1:1 allocation. The randomisation will be performed stratified by Overweight: Obese in a 2:1 ratio (e.g. 20 Overweight for every 10 Obese)

Sponsors

University College Dublin
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Primiparous women 2. Singleton pregnancy 3. BMI =25 kg/m2 at booking visit 4. 26 – 34 weeks’ gestation at recruitment 5. Aged =18 years 6. Good understanding of English 7. Ability to give informed consent 8. Have a support partner available and willing to participate in the trial if they are randomised to the intervention group. This support partner may be the infant’s father, the pregnant woman’s male or female partner, the pregnant woman’s mother or sister or a friend.

Exclusion criteria

Exclusion criteria: 1. Preterm (<37 weeks’ gestation) delivery 2. Any condition requiring medication that is contraindicated for breastfeeding

Design outcomes

Primary

MeasureTime frame
Feeding method assessed using self-reported questionnaires completed by the mother, Questionnaire on Infant Feeding (O’Sullivan et al., 2017) at 3 months postpartum

Secondary

MeasureTime frame
1. Intention to breastfeed following the antenatal component of the intervention, assessed by open ended and closed ended questions in a questionnaire completed by the mother at pre-antenatal class 2. Initiation rates of breastfeeding, collected using hospital discharge data at discharge from hospital 3. Exclusive and any breastfeeding prevalence. assessed using a questionnaire completed by the mother, Questionnaire on Infant Feeding (O’Sullivan et al., 2017), at hospital discharge, 6 weeks and 6 months postpartum 4. Maternal and support partner attitudes toward breastfeeding, assessed by open ended and closed ended questions in a questionnaire completed by the mother at pre-antenatal class, 6 weeks, 3 months, and 6 months postpartum 5. Breastfeeding self-efficacy, assessed using Breastfeeding Self-Efficacy Short Form (Dennis, 2003) at pre-antenatal class, 6 weeks, 3 months, and 6 months postpartum

Countries

Ireland

Outcome results

None listed

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