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The Mother in Norway Study

The Mother in Norway Study - A Randomised Trial of Nurse-Family Partnership (NFP)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05895604
Acronym
MiNS
Enrollment
700
Registered
2023-06-08
Start date
2023-06-01
Completion date
2042-12-31
Last updated
2025-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Injuries, Maternal Behavior, Mental Health Wellness, Violence

Brief summary

The Norwegian government is implementing the Nurse Family Partnership program (NFP) to combat child abuse and social inequality. This study will examine NFP with an individually randomized controlled parallel-group trial. The study will enroll 700 mothers over three years, with half receiving NFP services and the other half receiving standard care. The primary outcome is violence towards mothers and their children, assessed through questionnaires and observation tests. The study will also evaluate the program's effects on various health-related outcomes using administrative data. Cost-effectiveness analyses will be conducted to compare NFP to existing services and improve its delivery efficiency.

Detailed description

The Norwegian government has since 2015 been in the process of implementing the Nurse Family Partnership program (NFP) in Norway, as a possibly important part in their strategy to combat child abuse and social inequality. This study employs an individually randomized controlled parallel-group trial where participants are randomly assigned to experimental and control groups. The planned study population consists of 700 mothers to be enrolled over 3 years (June 2023-2026). Each participant will be individually randomized with a 50 percent probability of being assigned to the treatment group, and a 50 percent probability of being assigned to the control group. NFP services will be provided to those in the treatment group through the child's second birthday (2025-2029). The control group will receive the standard of care and whatever other programs and services are available in the community. Primary outcome is violence towards first-time mothers and their children. In their last trimester, and when the child is 6, 12 and 24 months old, mothers included in the study will receive a questionnaire assessing perceived partner violence, parenting skills, coping, control, and the child's development and language. At 24 months, staff at health stations will perform the Bayley observation test of the child´s development and language. The study will also utilise administrative data to assess the effects of NFP on a wide range of health- and health related outcomes. All analyses are carried out blinded. The investigators estimate intention-to-treat (ITT) effects and per-protocol analysis. Cost-effectiveness analyses will be conducted to compare the value of NFP to existing services, and to improve the efficiency in the delivery of NFP.

Interventions

Nurse-Family Partnership is a prenatal and infancy home visiting program providing regular visits to first-time mothers until the child is two years old

Sponsors

University of Oslo
CollaboratorOTHER
Norwegian Institute of Public Health
CollaboratorOTHER_GOV
The Norwegian Directorate for Children, Youth and Family Affairs
CollaboratorOTHER
Norwegian Center for Violence and Traumatic Stress Studies
CollaboratorOTHER
Regional centre for children and youth mental health and welfare
CollaboratorOTHER
Oslo Metropolitan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
16 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Female; No previous live births; Currently pregnant; Gestation period less than 28 weeks (i.e., less than or equal to 27 weeks, 6 days) at time of recruitment; Live within an area serviced by a NFP Implementing Agency; Not currently enrolled in the study; professionals are concerned about the pregnancy / impending parenthood

Exclusion criteria

Women who have had a previous live birth; Women who are not currently pregnant; Women who are past their 28th week of gestation (i.e., greater than or equal to 28 weeks, 0 days) at time of recruitment; Women who live outside of an area serviced by a NFP Implementing Agency; Women who are currently enrolled in the study; professionals are not concerned about the pregnancy / impending parenthood

Design outcomes

Primary

MeasureTime frameDescription
Domestic violence (change is being assessed)baseline, in last trimester, at 6, 12 and 24 months postpartumComposite Abuse Scale - Revised Short Form (CASr-SF). Items are scored on a scale ranging from 1-5, where higher scores indicate worse outcomes
Child maltreatment (change is being assessed)at 12 and 24 months postpartumBrief Child Abuse Potential Inventory (BCAPI). Items are scored on a dichotomous range (agree/disagree), where higher scores indicate better outcomes
Child welfare service reports24 months postpartumTotal number of reports to the child welfare service due to violence since birth
Child welfare service measures24 months postpartumTotal number of provided measures and care takeovers due to violence since birth
Injuries (change is being assessed)at delivery, 6, 12 and 24 months postpartumHospital admissions

Secondary

MeasureTime frameDescription
Health-related Quality of Life (change is being assessed)baseline, in last trimester, at 6, 12 and 24 months postpartumEQ-5D (the EuroQol Instrument), Items are scored on a scale ranging from 1-5, where higher scores indicate worse outcomes
Self-Efficacy (change is being assessed)at baseline, and at 6, 12 and 24 months postpartumGeneral Self-Efficacy Scale (GSE). Items are scored on a scale ranging from 1-4, where higher scores indicate better outcomes
Health behaviour (change is being assessed)baseline, in last trimester, at 6, 12 and 24 months postpartumUse of tobacco, alcohol, drugs
Parental Locus of Control (change is being assessed)at 6, 12 and 24 months postpartumParental locus of control (PLOC). Items are scored on a scale ranging from 1-5, where lower scores indicating internal control and higher scores indicating external control
Child Developmentat 24 months postpartumBayley scale of infant development
Parental skills (change is being assessed)at 6, 12 and 24 months postpartumParenting Sense of Competence Scale (PSOC). Items are scored on a scale ranging from 1-6, where higher scores indicate better outcomes
Interaction between mother and childat 12 months postpartumEmotional Availability Scale. Items are scored on a scale ranging from 1-7, where higher scores indicate better outcomes

Countries

Norway

Contacts

Primary ContactAnne Grete Tøge, phd
Anne-Grete.Toge@oslomet.no+47 67 23 81 58
Backup ContactEirin Pedersen, phd
Eirin.Pedersen@oslomet.no+47 936 36 150

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026