Effect of Ergonomic Practices on Quality of Breastfeeding
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: educational sessions and booklet, No Interventions.
- Who it may be relevant to
- Registry conditions: we Search for the Effect of Ergonomic Practices on Quality of Breastfeeding. Basic parameters: 18 years — 35 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Effectiveness of Ergonomic Practices on Quality of Breastfeeding Among Primiparous
Overview
This study aims to assess the effectiveness of ergonomic practices on quality of breastfeeding among primiparous.
Detailed description
Prolonged discomfort experienced during lactation can significantly impede a mother's adjustment to the maternal role. This discomfort arises from suboptimal body positioning and extended periods of sitting during breastfeeding and some mothers stop breastfeeding as a result of that. Consequently, the promotion of maternal comfort during breastfeeding will enhance the quality of breastfeeding, and this will be achieved by encouraging mothers to assume appropriate body mechanics, appropriate breastfeeding positions, and use breastfeeding pillows during breastfeeding. Therefore, the researcher will conduct the current study.
Interventions
- Other educational sessions and booklet
educational sessions and booklet about ergonomic practices during breastfeeding which include appropriate body mechanics , breastfeeding positions, and use of breastfeeding pillows. - Other No Interventions
In this group, the mothers will breastfeed their newborns according to the routine hospital postpartum instructions only.
Primary outcome measures
- A LATCH score [Time frame: At two weeks and two, four and six months after delivery]
Secondary outcome measures (1)
- Change in the growth chart of the infants [Time frame: At two weeks and two, four, and six months after delivery]
Eligibility criteria
Inclusion criteria
- 1\) Nulliparous women, 2) Mothers between the ages of 18 and 35, 3) Mothers who are in the third trimester, 4) Singleton pregnancy, 5) Mothers who have the intention of breastfeeding, and 6) Mothers who can read and write.
Exclusion criteria
- 1\) Mothers with nipple problems, such as flat or inverted nipples, and 2) Mothers with medical or surgical problems interfering with breastfeeding.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07098702 · effect of EP on QOB among pp