Compared to children receiving usual care, children receiving the NFP-intervention will have better birth outcome, growth and development, psycho-social outcomes and behavioral outcomes in the first years of life, and also later in life.
ID
Bron
Verkorte titel
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
At the start of the study women will be interviewd about their physical condition (diseases, diet, sigarette smoking, drug abuse, etc.), emotional (feelings of anxiety and depression, a history of abuse or neglect), relational (partner, social support), and social determinants (education, financiel problems, housing, use of current health care). Mothers' sense of control about her circumstances is determined. Partners are being asked to report emotional or behavioral problems. A urine sample will be taken to determine urinary infections.
During the entire study measurements of height and weight, breast- or bottle feeding, and development according to Van Wiechen, collected by the regular health system will be used in the study. Also, data of the delivery and first week after birth will be collected from the files of primary health care. At the age of 6 months, we measure development, anxiety and mother-child interactions. At the ages of 1 and 2 years the home situation will be observed according to safety, availability of food and fruit and of toys. At the age of 2 other determinants are: child abuse, finance, home, education, anti conception, pregnancies, stability relation with the father, psychopathology of the mother.
Achtergrond van het onderzoek
Implementation and research of the Nurse Family Partnership intervention, in which risk factors threathening the physical, the cognitive and the behavioral development during pregnancy and in the first 2 years of life are being reduced in yet-to-be-born children of high-risk mothers. The ultimate goal is to improve pregnancy and birth outcomes for mother and child, to improve personal development and the opportunities for education and work for the mothers in order to make her more available for her child.
The study design is besed on a trial with 456 selected pregnant hig-risk mother randomly divided into a control and an intervention group. The high-risk pregnant women will be visited regularly by nurses during pregnancy, after the child is born, and 6 months, 1 year and 2 years after birth. During these visits the nurses will systematically adress (1) changes in mothers' behavior to promote the infants' health and development and to improve mothers'living circumstances with an emphasis on the improvement of diet and physical health and the reduction of substance use during pregnancy, (2) the quality of supportive relationship, and (3) the link between the mother and the regular services.
Doel van het onderzoek
Compared to children receiving usual care, children receiving the NFP-intervention will have better birth outcome, growth and development, psycho-social outcomes and behavioral outcomes in the first years of life, and also later in life.
Onderzoeksproduct en/of interventie
The Nurse Family Partnership intervention exists of an intensive schedule of approximately 30 home visits (maximal 60) by experienced youth health nurses. The home visits will start from the 16th week of pregnancy en will last until the child is 2 years of age. The frequency is about 2 visits each month with a higher frequency (once a week) in the first month of the programme and the first 6 weeks after birth, with a declining frequency (once a month) in the last 4 months. Every home visit lasts 1 to 1.5 hours.
Control: care as usual.
Publiek
Van der Boechorststraat 7
Mieke Haan de
Amsterdam 1081 BT
The Netherlands
+ 31 20-4448108
mi.dehaan@vumc.nl
Wetenschappelijk
Van der Boechorststraat 7
Mieke Haan de
Amsterdam 1081 BT
The Netherlands
+ 31 20-4448108
mi.dehaan@vumc.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. No previous born child (a number of pregnant women did have an abortion);
2. Pregnancy duration of maximum 28 weeks;
3. Low education grade;
4. Some knowledge of the Dutch language; 5. Furthermore, one or more of the following secundary inclusion criteria: no (supportive) social network or partner, alcohol - or drugabuse, actual violence in family or partner, history of abuse, psychologic problems such as anxiety or depression, non-realistic approach about motherhood, drop-out of school, unemployed, financial or housing-problems.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Heavy psychiatric problems or obvious psychosis;
2. Heavy drugs- or alcohol-addiction.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL840 |
| NTR-old | NTR854 |
| Ander register | : N/A |
| ISRCTN | ISRCTN16131117 |