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Not yet recruiting NCT07336004

Breastfeeding: Influencing Determinants, Knowledge and Self-efficacy

— Observational Breastfeeding, Exclusive Breastfeeding Initiation

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Breastfeeding, Exclusive, Breastfeeding Initiation. Basic parameters: 15 years — 49 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 →

Unsure about the terms? Read our patient guide →

Official title

Breastfeeding: Influencing Determinants, Knowledge and Self-efficacy Among Lactating Mothers in Sohag Governorate

Overview

Our study will assess the prevalence of exclusive breastfeeding and the determinants and assess knowledge and self efficacy of lactating mothers towards breastfeeding

Primary outcome measures

  • timely initiation of breastfeeding [Time frame: two years]
  • exclusive breastfeeding [Time frame: two years]
Secondary outcome measures (2)
  • Breastfeeding knowledge [Time frame: two years]
  • Breastfeeding self-efficacy [Time frame: two years]

Eligibility criteria

Inclusion criteria

  • The study will include lactating mothers with children from day zero to 24 months.

Exclusion criteria

  • Mothers with absolute contraindications to breastfeeding as the infant having classic galactosemia
  • The mother having human immunodeficiency virus (HIV) will be excluded from the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07336004 · Soh-Med--25-12-3MD

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗