Actively Recruiting
Client-Centered Breastfeeding Support: Effects on Primipara Mothers in a Randomized Trial Breastfeeding Self-Efficacy, Attitudes, and Problems in Primiparous Mothers: A Randomized Controlled Trial
Led by Pamukkale University · Updated on 2024-11-19
45
Participants Needed
1
Research Sites
104 weeks
Total Duration
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AI-Summary
What this Trial Is About
Study Description The goal of this randomized controlled trial is to examine the effects of a client health behavior interaction model-based breastfeeding support program on breastfeeding self-efficacy, attitudes, and problems in primipara mothers. The main questions it aims to answer are: 1. How does the program influence mothers' self-efficacy in breastfeeding? 2. What impact does the program have on mothers' attitudes towards breastfeeding and the problems they encounter? Participants will: 1. Receive breastfeeding support through an interactive health behavior model. 2. Participate in assessments of their breastfeeding self-efficacy and attitudes at designated intervals throughout the study duration. There is a comparison group: 1\. Researchers will compare the intervention group (mothers receiving the structured program) to a control group (mothers receiving standard care) to see if there is a significant difference in outcomes related to breastfeeding self-efficacy, attitudes, and encountered problems.
CONDITIONS
Official Title
Client-Centered Breastfeeding Support: Effects on Primipara Mothers in a Randomized Trial Breastfeeding Self-Efficacy, Attitudes, and Problems in Primiparous Mothers: A Randomized Controlled Trial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Primiparous mothers
- Gestational age between 32 and 40 weeks
- Ability to communicate effectively
- Ownership of a smartphone
- Minimum education level of primary school graduate
You will not qualify if you...
- Infants with health issues
- Mothers with medical or pregnancy-related complications that hinder breastfeeding, including heart disease, cancer, nephritis, active or untreated tuberculosis, HIV/AIDS, active herpes lesions on the breast, or severe malnutrition
- Participants undergoing infertility treatment with IVF
AI-Screening
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Trial Site Locations
Total: 1 location
1
Pamukkale University Family Health Center
Denizli, Pamukkale, Turkey (Türkiye), 20100
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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