To identify high risk groups who are in need for more and specific help and guidance, and to offer appropriate counselling.
ID
Source
Brief title
Condition
- Congenital and hereditary disorders NEC
- Anxiety disorders and symptoms
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
• Symptoms of PTSD.
• Symptoms of psychopathology.
Secondary outcome
1. cognitive appraisals childbirth
2. cognitive coping
Background summary
o What is the prevalence of probable PTSD and psychopathology in general two
years after the diagnosis of congenital anatomical anomalies?
o Does the amount of symptoms of PTSD and of psychopathology become less in
time?
o Which factors (medical, psychological, demographic) have an influence on the
amount of symptoms of PTSD and on the amount of symptoms of psychopathology?
Study objective
To identify high risk groups who are in need for more and specific help and
guidance, and to offer appropriate counselling.
Study design
A prospective design.
Study burden and risks
Parents will be followed from the diagnosis of congenital anatomical anomalies
until two years after the birth of their child.
Inclusion will start after the prenatal diagnosis as from 20 weeks gestation OR
after the postnatal diagnosis 6 weeks after the birth of the child.
Then measurements will be done 6 months, 1 year, and 2 years after the birth of
the child. At each measurement parents will receive a set of 3 - 4
questionnaires; it will take approximately 30 minutes to fill these in.
Dr. Molewaterplein 60
3000 CB ROTTERDAM
NL
Dr. Molewaterplein 60
3000 CB ROTTERDAM
NL
Listed location countries
Age
Inclusion criteria
Parents who are expecting a child with major congenital anatomical anomalies will be asked to participate. The anomalies are:
1.(isolated or associated) congenital diaphragmatica hernia,
2. (isolated or associated) esophageal atresia,
3. and (isolated) intestinal atresia.
Exclusion criteria
1. Parents who are expecting a child with other major congenital anomalies than a congenital diaphragmatica hernia, esophageal atresia or intestinal atresia.
2. Single parent families.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| CCMO | NL13825.078.06 |