Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03659721
Other study ID # VIVE 100750-751
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 1, 2018
Est. completion date March 31, 2023

Study information

Verified date February 2023
Source VIVE - The Danish Center for Social Science Research
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial is a randomized controlled trial with the aim is to assess the effectiveness of Family Clinic and Municipality (FACAM) to improve mother-child relationship, maternal health, maternal mental health, and the development and well-being of the child.


Description:

Pregnant women who struggle with psychosocial challenges during pregnancy have a higher risk of preterm birth, giving birth to a child with low birth weight and a higher risk of complications during pregnancy both for mother and child. An early and coordinated intervention to reduce inequality in health may be important for this group of vulnerable women. The FACAM intervention is developed in Odense with the aim of reducing inequality in health by giving vulnerable pregnant women and their children the best possible start in life by offering an interdisciplinary coordinated support. The support will be offered by Odense municipality, the family clinic (Familieambulatoriet), and local voluntary organizations. The aim of the trial is to assess the effectiveness of FACAM to improve mother-child relationship, maternal health, maternal mental health, and the development and well-being of the child. The study is a Randomized Controlled Trial (RCT). A total of 320 pregnant women will be randomized to FACAM or Care as Usual. Participants are pregnant women categorized as antenatal care group 3 or 4, living in Odense and with a referral to Familieambulatoriet, OUH. Participants must be able to fill out questionnaires in Danish or English. Data will be collected at baseline (pregnancy), and when the child is 3 and 12 months old.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 332
Est. completion date March 31, 2023
Est. primary completion date March 31, 2023
Accepts healthy volunteers No
Gender Female
Age group 15 Years and older
Eligibility Inclusion Criteria: - Pregnant women admitted to the Familieambulatorium, and living in Odense municipality - Antenatal care group 3 or 4 according to the Danish health authorities' recommendations Exclusion Criteria: - Life-threatening illness in parent or child - Not able to fill out questionnaires in Danish or English - Child in out of home care after birth - Pregnancy with twins - Previous participation in the FACAM project

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
FACAM
Support person
Care as Usual
Usual care
COS-P
Attachment based therapy

Locations

Country Name City State
Denmark VIVE - The Danish Centre of Social Science Research Copenhagen
Denmark Odense University Hospital Odense

Sponsors (5)

Lead Sponsor Collaborator
VIVE - The Danish Center for Social Science Research Odense Kommune, Odense Patient Data Explorative Network, Odense University Hospital, Syddansk Universitet

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Maternal sensitivity Maternal sensitivity measured by the CIB (Coding Interactive Behavior) at child age 12 months
Secondary Maternal Sensitivity Maternal sensitivity measured by the CIB (Coding Interactive Behavior) at child age 3 months
Secondary Coding interactive bahavior (CIB) Parent child relationship Subscales: Intrusiveness, Limit setting, Involvement, Withdrawal, Reciprocity, Negative states child age 3 and 12 months
Secondary Ages and Stages Questionnaire-Social Emotional 2 (ASQ:SE-2) Child social-emotional Development Total score range 0-150 ( 3 months 15 items), 0-260 (12 months 26 items). Low score is better. child age 3 and 12 months
Secondary Edinburgh Postnatal depression Scale (EPDS) Depression Total score range 0-30. Low score is better child age 3 and 12 months
Secondary Warwick-Edinburgh Mental Well-being Scale Maternal mental Health 7 items. A total score i calculated by summing the 7 items and converting the raw score according to a published conversion table. Raw score range 7- 35. Converted score range 7-35. High is better outcome. child age 3 and 12 months
Secondary Prenatal Parental reflective functioning questionnaire (P-PRFQ) Parental reflective functioning for pregnant women. Total score range 14-98. Higher score is better. Three subscales:
Opacity of mental states (4 items), reflecting on the fetus-baby (3 items) and Dynamic of mental states (5 items)
Baseline
Secondary Parental reflective functioning questionnaire (PRFQ-1) Parental reflective functioning Three subscales score range 6-42: Pre-Mentalizing Modes (PRFQ-PM) 6 items. low score is better. Certainty about Mental States (PRFQ-CMS) 6 items high score is better. Interest and curiosity in mental states PRFQ-IC 6 items high score is better. child age 12 months
Secondary Parental Stress Scale (PSS) Parental stress Total score range 18-90 low score is better Cild age 3 and 12 months
Secondary Ages and Stages Questionnaire 3 (ASQ:3) Child development child age 3 months
Secondary Activities with child Singing and reading Total score range 0-70. High score is better. child age 12 months
Secondary Being a Mother (BAM-13) Maternal confidence. Total score range 0-39. Low score is better child age 3 and 12 months
Secondary Hospital Anxiety and Depression Scale (HADS) Two subscales Anxiety (range 0-21 low score is better) and depression (range 0-21 low score is better) Baseline, 3 and 12 months
Secondary Experiences in Close Relationship Scale-Short Form (ECR-S) Two subscales Anxiety (range 1-42 low score is better) and Avoidance (range 1-42 low score is better) Baseline