MTB: The Effectiveness of MInding the Baby in a Danish Community Sample

Sponsor
VIVE - The Danish Center for Social Science Research (Other)
Overall Status
Recruiting
CT.gov ID
NCT03495895
Collaborator
Yale University (Other), Metodecentret - Center for Effective Innovation in Social Services (Other)
250
1
2
71.7
3.5

Study Details

Study Description

Brief Summary

Minding the Baby is an intensive and preventive home-visiting programme that helps vulnerable or high risk mothers. MTB is delivered by an interdisciplinary team. Ten Danish sites will be randomized to training at time 1 or 2 and recruit usual care control families before they receive the training. Families are assessed before they give birth and when their child is three months, one and two years old with a range of assessments including maternal sensitivity, parent mental Health, child development, and health related register data. The aim of the trial is to assess the effectiveness of Minding the Baby to improve mother-child relations and the mental health of parents and children.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Minding the Baby
  • Behavioral: Usual Care
N/A

Detailed Description

Minding the Baby is an intensive and preventive home-visiting programme that helps vulnerable or high risk mothers. The focus of the intervention is to reduce negative infant and maternal outcomes and strengthen the attachment relationship. MTB is delivered by an interdisciplinary team of highly skilled practitioners, who have health and social work experience, integrating advanced practice nursing and mental health care for mothers and infants. In the proposed Randomised Control Trial (RCT) the investigators will study the efficacy of this innovative intervention across ten Danish sites. Site staff will be trained at two sessions one year apart. Sites are randomized to training at time 1 or 2. All sites will recruit treatment as usual control families before they receive the training and start offering the intervention to all families. Potential participants will be approached by a local front staff member (e.g. midwife, helath visitor or social worker) who will inform mothers of the project in the early pregnancy. Consenting eligible participants will be assessed before they give birth and when their child is three months, one and two years old.

The effectiveness of the MTB programme will be evaluated by assessing a range of maternal and infant outcomes, including maternal sensitivity, parent mental Health, child development, and register data on e.g. infant maltreatment and neglect, hospitalization, income, immunization. By combining parent report, observational and register data researchers will get a unique opportunity to advance knowledge regarding effective ways to support some of the youngest and most vulnerable children in Denmark.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
250 participants
Allocation:
Randomized
Intervention Model:
Sequential Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
As the intervention is a home visiting intervention participants and care providers cannot be blinded. Outcome assessor and data analyst will be blinded.
Primary Purpose:
Treatment
Official Title:
The Effectiveness of MInding the Baby in a Danish Community Sample
Actual Study Start Date :
Jun 10, 2018
Anticipated Primary Completion Date :
Jun 1, 2022
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Minding the Baby

Families are visited weekly beginning in the mother's third trimester of pregnancy up through the child's first birthday, at which point visits take place biweekly up through the child's second birthday.

Behavioral: Minding the Baby
Visits are carried out on an alternating basis by a team made up of a nurse practitioner (NP) and social worker.

Other: Control

Usual care control condition. Families in the control Group receive the usual care that is offered to families in the target group

Behavioral: Usual Care
Usual care condition

Outcome Measures

Primary Outcome Measures

  1. Maternal sensitivity measured by the CIB (Coding Interactive Behavior) [at child age 24 months]

    Maternal sensitivity

Secondary Outcome Measures

  1. Maternal sensitivity measured by the CIB (Coding Interactive Behavior) [Child age 12 months]

    Maternal sensitivity

  2. Coding interactive bahavior (CIB) [child age 12 and 24 months]

    Parent child relationship Subscales: Intrusiveness, Limit setting, Involvement, Withdrawal, Reciprocity, Negative states

  3. Ages and Stages Questionnaire-Social Emotional 2 (ASQ:SE-2) [3, 12 and 24 months]

    Child social-emotional Development Total score range 0-150 ( 3 months 15 items), 0-260 (12 months 26 items), 0-300 (24 months 30 items). Low score is better.

  4. Edinburgh Postnatal depression Scale (EPDS) [3, 12 , 24 months]

    Depression Total score range 0-30. Low score is better

  5. Warwick-Edinburgh Mental Well-being Scale [Baseline, 3, 12 , 24 months]

    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.

  6. 2-5 [24 months]

    The name of the measure is 2-5 and measures child Development. Subscales included: Perception (7 items) low score is better, Language (10 items) low score is better

  7. Prenatal Parental reflective functioning questionnaire (P-PRFQ) [Baseline]

    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)

  8. Parental reflective functioning questionnaire (PRFQ-1) [12 and 24 months]

    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.

  9. Parental Stress Scale (PSS) [12 ,24 months]

    Parental stress Total score range 18-90 low score is better

  10. Ages and Stages Questionnaire 3 (ASQ:3) [3 months]

    Child development

  11. Acitvities with child [12 and 24 months]

    Singing and reading Total score range 0-70. High score is better.

  12. SEAM Family profile [12 months]

    Family profile

  13. Parent behavior Inventory (PBI) [12 and 24 months]

    Parent Behavior. Two subscales Supportive/Engaged and Hostile/Coercive.

  14. Being a Mother (BAM-13) [3 months]

    Maternal confidence. Total score range 0-39. Low score is better

  15. Hospital Anxiety and Depression Scale (HADS) [Baseline, 3, 12,24 months]

    Two subscales Anxiety (range 0-21 low score is better) and depression (range 0-21 low score is better)

  16. PTSD-8 [Baseline, 12 and 24 months]

    A Short PTSD Inventory. Total score range 8-32, low score is better

  17. Experiences in Close Relationship Scale-Short Form (ECR-S) [Baseline, 12, 24 months]

    Two subscales Anxiety (range 1-42 low score is better) and Avoidance (range 1-42 low score is better)

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Pregnant vulnerable women
Exclusion Criteria:
  • Current severe substance abuse

  • Severe psychotic illness

  • Profound or severe learning disabilities

  • Life-threatening illness in parent or child

  • Non-Danish speaking

Contacts and Locations

Locations

Site City State Country Postal Code
1 VIVE - The Danish Centre of Applied Social Science Copenhagen Denmark 1052

Sponsors and Collaborators

  • VIVE - The Danish Center for Social Science Research
  • Yale University
  • Metodecentret - Center for Effective Innovation in Social Services

Investigators

  • Principal Investigator: Maiken Pontoppidan, Ph.D., VIVE

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Maiken Pontoppidan, Researcher, VIVE - The Danish Center for Social Science Research
ClinicalTrials.gov Identifier:
NCT03495895
Other Study ID Numbers:
  • VIVE
First Posted:
Apr 12, 2018
Last Update Posted:
Dec 17, 2021
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Maiken Pontoppidan, Researcher, VIVE - The Danish Center for Social Science Research

Study Results

No Results Posted as of Dec 17, 2021