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Pilot Trial of Family Partner - a Child Maltreatment Prevention Intervention

Family Partner -Co-development, Implementation and Evaluation of a Child Maltreatment Prevention Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04957394
Acronym
FAMPART
Enrollment
45
Registered
2021-07-12
Start date
2022-01-01
Completion date
2024-09-18
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

Child Maltreatment, Family, Parenting

Brief summary

Prior to this pilot study, it is unclear whether comparing a manualized version of the Family Partner Model to standard practice in the Child Welfare Services would be feasible. Results will inform whether and how to design a fully powered randomized controlled trial to test the effects of a manualized version of the Family Partner Model on child maltreatment. The specific results of the pilot study will inform 1) randomization procedures, 2) data sources to be used, 3) sample size calculations, and 4) adaptations to the design and measures for a fully powered randomized controlled trial.

Detailed description

The objective is to assess the adaptability and acceptability of the Family Partner Intervention, and the feasibility of a future randomised controlled trial. Our specific research questions are: 1. What is the adaptability, acceptability, and feasibility of the Family Partner intervention in a Norwegian municipal context? 2. What are the experiences and possible outcomes of the Family Partner intervention? 3. Is the trial design feasible for an RCT expansion? The investigators will pilot a parallel randomized trial (RCT), allocated to two groups (treatment and control). Families that fit to the target group, will be invited to take part in the study. Each family which fit the inclusion criteria and consent to participate will be randomized with a 1:1 allocation to experimental and control groups. Each Family Partner can serve 5 families at a time, and the Family Partner will serve families from 6-18 months. As families complete the programme, new families will be recruited. Hence, the recruitment and randomization will be an ongoing process. Any changes to methods after pilot trial commencement will be reported along with study results. In a future RCT, the objective is to evaluate the effectiveness of the Family Partner Intervention, i.e. whether introducing the intervention would improve the outcome of existing Child Welfare Services. Hence, the trial is a superiority trial, in which the Family Partner Intervention is hypothesized to be superior to existing service provision. The trial is designed according to an intention-to-treat principle, where all consented participants are included in the analyses, independent of their adherence to intervention.

Interventions

BEHAVIORALFamily Partner

The Family Partner intervention is based on well-known elements for preventing child abuse and neglect, such as 1) high intensity intervention with home visitations, 2) coordination of services, 3) an ecological perspective, 4) parental guidance, and 5) an emphasis on a therapeutic relationship with parents to create trust, change and agency. Family Partners must have relevant professional background and education, such as social work, child welfare services and other health/welfare occupations. They must have a personal attitude for relation-based service delivery in a home-setting, a long work experience and in-depth knowledge of municipal welfare services. Each practitioner will follow five families. The estimated duration of the intervention is 12 months, but might go over longer stretches of time if it is considered beneficial for the families. The minimum duration of the intervention is 3 months.

Sponsors

SOS Children's Villages, Norway
CollaboratorUNKNOWN
Øvre Eiker municipality
CollaboratorUNKNOWN
Lillehammer municipality
CollaboratorUNKNOWN
Oslo Metropolitan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* parents are 18 years or older, and * children are under 18 years, and * families with complex challenges who are already involved in the Child Welfare Services, and * children live under potentially harmful circumstances, and * parents struggle in several areas, e.g. employment, poverty, drug misuse, mental health

Exclusion criteria

None

Design outcomes

Primary

MeasureTime frameDescription
AcceptabilityAcceptability at 12 monthsIntervention Rating Profile (IRP-15)

Secondary

MeasureTime frameDescription
Relationship between the Family Partner and the parentsChange from Baseline WAI at 3, 6, 9, 12, 15 and 18 monthsThe Working Alliance Inventory (WAI)

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026