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临床试验/IRCT2017041810426N16
IRCT2017041810426N16已完成未知

Evaluation of the effect of consultation based on Bristol tool on self-efficacy and continuation of breast- feeding among primi-parous women undergoing cesarean section.

Hamadan University of Medical Sciences0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
15 years 至 49 years(—)
性别
Female

入选标准

  • Cesarean section delivery; primiparous; literacy; Residency in Hamadan city; Having a mobile number for follow-ups; Singleton birth and term delivery. Exclusion criteria: Inability to do breastfeeding according to physician’s approval; Problems after cesarean section such as bleeding and anesthesia related problems; Underlying disease in mother such as cardiac, pulmonary, chronic and infection diseases; Addiction; Neonatal abnormality and diseases.

排除标准

  • 未提供

研究者

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