Effectiveness of Midwife Phone Support With the to Reduce the Early Abandonment of Breastfeeding
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 220
- 主要终点
- Percentage of participants who breast-feed at 3 months of intervention
研究概览
简要总结
Objective: To evaluate the effectiveness of telephone support of the reference midwife, in relation to the abandonment of breastfeeding of primiparous mothers and to identify, both the risk factors and the protective factors for the early abandonment of breastfeeding.
Material and Method Randomized parallel controlled clinical trial.
详细描述
Sample: 220 primiparous mothers with access, during the 8 weeks postpartum, to a mobile phone to contact the midwife randomization of 110 mothers to the experimental group and 110 to the control group. The mothers of the experimental group will be offered the mobile phone number to contact their midwife after delivery. The mothers of the control group will receive the usual attention of the portfolio of services that includes the spontaneous visit in the center, the telephone call in the center, the home visit and the health education groups.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Primiparians who carry out the follow-up of pregnancy for the midwife
- •The pregnant woman is of low risk
- •Possibility of the mother to make calls to the mobile phone.
- •The pregnant woman wishes to participate in the study.
排除标准
- •Maternal or fetal pathology that can condition maternal breastfeeding.
- •idiomatic barrier.
- •Prematurity.
- •Baby with weight <2,500 gr. at birth
- •Home delivery during the puerperium
研究组 & 干预措施
Intervention group
Mothers received a phone support service with their midwife during the 8 weeks after childbirth.
干预措施: Phone care support by midwife (Other)
Control group
Mothers received standard postpartum care
结局指标
主要结局
Percentage of participants who breast-feed at 3 months of intervention
时间窗: 3 months
Women who still breastfeed 3 months after the intervention with respect to the control arm
次要结局
未报告次要终点