跳至主要内容
临床试验/NL-OMON43819
NL-OMON43819招募中不适用

From expecting to experiencing: The role of parenting cognitions in the transition to parenthood - Parenthood: From expecting to experiencing

Vrije Universiteit0 个研究点目标入组 1,850 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,850

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
18 至 99(—)

入选标准

  • Inclusion criteria for samples I, II, and for sample C : First pregnancy or previous pregnancy which ended in a miscarriage before 10 weeks. Supplementary inclusion criteria sample II: Pregnancy in week 20-22 . Supplementary inclusion criteria sample III: pregnant women considered to be at higher risk of having a baby with a congenital abnormality, based on advanced ultrasonography between 14-32 weeks of gestation.
  • Supplementary inclusion criteria for sample C a. Pregnant women who have been in contact with mental health services or child protection agencies before the age of 18, who are currently in contact with mental health care or who had one or more traumatic experience before the age of 18. b.Positive screening for depression (BDI >13) and / or positive screening for anxiety disorder (STAI > 40) on at least one timepoint during pregnancy. c. Negative screening for depression (BDI<13) and anxiety disorder (STAI<40) at all time points during pregnancy. This sample (controle groep) is taken from the larger cohort of study II.
  • Supplementary inclusion criteria sample for Study VI: a. Participants from Sample C: childhood trauma, ACE score > 4. b.Participants from sample 2: Absence of childhood trauma, indicated by responses to the Adult Attachment Interview (question 9), negative screening depression and anxiety on all measurements (BDI <13 and STAI <40), and age mother between 18 and 35. Supplementary inclusion criteria Follow-up study (2 years postpartum): participation in study 1, 2 or project C. Supplementary inclusion criteria Follow-up study (4 years postpartum)- part A and B: participation in study 1, 2 or project C. Study 6: participation in Study 2 or C. Follow-up study (7 years postpartum): participation in study 1, 2 or project C.

排除标准

  • Exclusion criteria for sample I, II, III and sample C: Insufficient mastery of Dutch language. Supplementary exclusion criteria for sample II, and sample C: a. prenatal diagnosis of a congenital abnormality b. Abortion or interruption of pregnancy before 24 weeks pregnancy. Supplementary exclusion criteria for Sample III: a. Pregnant women considered to be at higher risk of having a baby with a congenital abnormality, based on invasive diagnostics early in pregnancy (10-12 weeks). b. Isolated growth delay of the fetus. c. Pregnant women with possible congenital abnormality, based on ultra-sound scans at a centre of primary care, but not confirmed at the VUmc or other specialized centres. d. Previous pregnancy of a child with a congenital abnormality. e. Insufficient mastery of Dutch or English language. Supplementary exclusion criteria for sample VI: participants from sample C: child with a congenital abnormality. Participants from sample 2:one or more childhood trauma's (AAI), positive screening anxiety and depression (STAI > 40 en/ of BDI >13) and child with a congenital abnormality.

研究者

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