From expecting to experiencing: The role of parenting cognitions in the transition to parenthood
- Conditions
- congenitale aandoeningen, niet nader gespecificeerdnvt10002861
- Registration Number
- NL-OMON43819
- Lead Sponsor
- Vrije Universiteit
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 1850
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.
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method