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临床试验/IRCT2016060428240N1
IRCT2016060428240N1已完成2 期

Clinical trial comparing the effectiveness of desensitization integration in preparation for childbirth classes to pregnant women anxiety that participate in regular classes in preparation for childbirth

Vice Chancellor for research; Shahroud University of Medical Sciences0 个研究点目标入组 76 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
76

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
20 years 至 35 years(—)
性别
Female

入选标准

  • Inclusion criteria consisted of: Causing the first being about 20 weeks gestational age, age between 20 and 35 years, the same anxiety (Business forget of 20 to 69 in Scale anxiety, including anxiety is mild to moderately severe), lack of medical-surgical diseases ( Blood pressure, diabetes),No history of psychiatric or mental illness, and the normal healthy fetus in the first trimester graphic examination (without any fetal abnormalities, the normal location of the placenta, normal cervical length)?No apparent obstacles for normal delivery at the time of sampling, any contraindications to vaginal delivery, having the symptoms of threatened abortion, have at least read and write, singleton pregnancy, non-smoking, drugs and alcohol, single spouse, Lack of recurrent miscarriage and infertility. Exclusion criteria: absence of more than two sessions, moved, and the unavailability of pregnant women and pregnancy termination for any reason before the end of counseling, the creation of any indication for cesarean delivery.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research; Shahroud University of Medical Sciences

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