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The Effect of Relactation Support Program on Milk Release

The Effect of Relactation Support Program on Milk Release, Mother-Infant Attachment and Maternity Role

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06437093
Enrollment
34
Registered
2024-05-31
Start date
2021-10-01
Completion date
2022-10-22
Last updated
2024-05-31

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

Conditions

Breast Feeding, Exclusive, Mother-Child Relations

Keywords

breast feeding, connecting, maternal role

Brief summary

Aim: This study aimed to determine the effect of relactation support program on milk release, mother-infant attachment and maternity role. Materials and Methods: This single-group pre-test post-test experimental study was conducted with 34 mothers who had 1-4 month old infants, stopped breastfeeding at least 15 days and at most 3 months ago and were registered in the family health centers of a province in the southern Turkey. The relactation support program was completed in 15 days, with eight home visits and seven telephone support sessions. The data were collected using a personal information form, a mother-infant follow-up form, the Maternal Attachment Inventory (MAI) and the Barkin Index of Maternal Functioning (BIMF). Keywords: Mother-Infant Attachment, Maternity Role, Midwifery, Relactation, Milk Release.

Detailed description

This is a single-group pre-test post-test experimental study. This study was conducted between October 2021 and October 2022 in Family Health Centers (FHCs) in province in southern Turkey. By using the G\*power 3.1 program, the sample size was determined to include 29 mothers/women under 5% margin of error, 95% confidence level, and 95% power of representation.

Interventions

OTHERTEACHING RELACTATION TECHNIQUES

In our midwifery intervention, the mother was firstly educated about breastfeeding and relactation, using educational brochures prepared by the researchers. Afterwards, the mother was taught nipple stimulation, skin-to-skin contact and finger feeding method, and the first feeding of the baby was performed together with the mother. After this first intervention in the FHC, all interventions were performed at home. The follow-ups continued for 15 days with one day of telephone support and one day of home visit. Since the majority of mothers did not accept video calls (privacy, etc.), telephone support was provided only verbally.

Sponsors

Inonu University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

This is a single-group pre-test post-test experimental study.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

For mothers; * Having no milk release, * Using no pharmacological agents that may increase milk release, * Being not pregnant, * Having no communication problem, * Being literate, * Being between the ages of 18-35 years, * Having singleton gestation in their last childbirth, * Using no medication that prevents breastfeeding (chemotherapy, etc.). For babies; * Being healthy * Having no congenital sucking problem (cleft palate, cleft lip, etc.)

Exclusion criteria

For mothers; * Using any pharmacologic agent to increase milk release, * Having a diagnosis of psychiatric illness. For babies; * Having any metabolic disease that may prevent breastfeeding (galactosemia, phenylketonuria, etc.) or any other chronic disease (advanced heart disease, etc.).

Design outcomes

Primary

MeasureTime frameDescription
QuestionnaireFirst dayMother-Infant Follow-Up Form filled out at the first meeting with the participants.This form was prepared by the researchers and includes information about the mothers' breastfeeding issues, breast health problems (cracks, mastitis, etc.), number of daily breastfeeding, number of daily milk release, amount of milk release, baby's weight and presence of sucking problems, which should be followed up during relactation.
Scale 1First dayMaternal Attachment Scale was used for pretest.This 4-point Likert-type scale has a total of 26 items, scoring as always =4, often =3, sometimes =2, and never =1. The lowest and highest scores on the scale are 26 and 104, respectively. Higher scale scores refer to greater maternal attachment.
Scale 2First dayBarkin Index of Maternal Functioning Scale was used for pretest. Index of Maternal Functioning consists of 16 items, scoring as completely disagree=0, disagree=1, partially disagree=2, undecided=3, partially agree=4, agree=5, completely agree=6. The lowest and highest scores on the scale are 0 and 96, respectively. The scale has five subscales: * Self-Care (2, 11, 13 items) * Maternal Psychology (8, 10 items) * Infant Care (items 12, 14, 15, 16) * Social Support (items 6, 7, 9) * Maternal adjustment (items 1, 3, 4, 5).

Secondary

MeasureTime frameDescription
Questionnaire1-16 daysMother-Infant Follow-Up Form was filled out every day for 15 days.Finally, it was filled on the 16th day.
Scale 1 Scale 1 (Attachment Inventory)16. dayMaternal Attachment Scale was used for posttest.
Scale 216. dayThe Barkin Index of Maternal Functioning was used for posttest.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026