- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02294968
The Family Startup Program. A Randomized Controlled Trial of a Universal Group-based Parenting Support Program (FIV)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Some knowledge exists about effectiveness of high-intensity delivery of parenting support to subsets of at risk families. To the best of our knowledge, however, little is known about effects of universal primary prevention programs.
The Family Startup Program is a structured format for implementing pre- and postnatal parenting support groups that prepare new families for their roles as parents as well as focus on enhancing parents' social network. The Family Startup Program gathers couples in groups and introduces participants to informal sources of support (e.g. by meeting and interacting with other new families) and to a broad range of community resources (e.g. financial advisers, child dentist, local solicitors, family counselors) providing them with information and parenting skills. The program content includes handling family finance, choice of paternity leave, couple communication, breastfeeding, network formation, ensuring dental health, sensitivity toward child signals, child rearing discipline, help-seeking behavior, home safety, and more.
A second formulated rational behind the program is that strengthening father involvement, social network formation and access to family services will serve to enhance family relationships, including parenting, coparenting and couple relationship quality. Through participation in Family Startup, families receive a long term connection with a health visitor in the community and are introduced to a broad range of community services. This can be expected to benefit optimal health service utility and ease access to resources for families and children with need. Improved child outcome are the ultimate goal. No scientific evaluation of program effects of the Family Startup program on child or family outcome was previously conducted.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Aarhus N, Denmark, 8200
- Aarhus University Hospital, Skejby
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
-Parents, mothers as well as their partners, expecting their first child in the municipality of Aarhus are eligible for the study. This is because of the universal nature of the original program. Mothers are included if interested regardless of the fathers' decline. Biological fathers, registered partners, as well as non-registered partners are eligible.
Exclusion Criteria:
- Parents are excluded from the study if they are under the age of 18 years
- Not capable of managing own legal affairs
- Choose not to accept any routine pregnancy scans. These exclusion criteria are chosen to secure that study participants are legally responsible and that we are able to recruit them via the Department of Obstetrics and Gynaecology in connection with the nuchal translucency scan around week 12
- The father or partner is not included if the mother declines participation. The mother can choose to attend the Family Startup Program with a friend (i.e. a sister, friend or neighbor) but friends are not eligible for the study
- Finally, individuals are excluded if they are not able to understand the Danish oral presentation of the study information and hence cannot give informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Family Startup
Family Startup plus usual pre- and postnatal care
|
Manualized parenting support program; see Center for Socialt Ansvar (2013)
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|
No Intervention: Control
Usual pre- and postnatal care
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The Parenting Sense of Competence scale (PSOC)
Time Frame: measured when child is 9 months
|
measured when child is 9 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The Parenting Sense of Competence scale (PSOC)
Time Frame: measured when child is 18 months
|
measured when child is 18 months
|
|
Parenting Stress Scale
Time Frame: measured when child is 9 months
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measured when child is 9 months
|
|
Breastfeeding duration
Time Frame: Duration before child is 9 months
|
Duration before child is 9 months
|
|
Couple Satisfaction Index
Time Frame: measured when child is 9 months
|
measured when child is 9 months
|
|
Coparenting Relationship Scale
Time Frame: measured when child is 9 months
|
measured when child is 9 months
|
Other Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
number of visits to the general practitioner
Time Frame: measured when child is 9 months
|
measured when child is 9 months
|
|
Ages and Stages Questionnaire
Time Frame: measured when child is 9 months
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measured when child is 9 months
|
|
School starting age
Time Frame: Before child is 8 years old
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Before child is 8 years old
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Marianne Simonsen, PhD, University of Aarhus
Publications and helpful links
General Publications
- Trillingsgaard TL, Maimburg RD, Simonsen M. Group-based parent support during the transition to parenthood: Primary outcomes from a randomised controlled trial. Soc Sci Med. 2021 Oct;287:114340. doi: 10.1016/j.socscimed.2021.114340. Epub 2021 Aug 30.
- Trillingsgaard T, Maimburg RD, Simonsen M. The Family Startup Program: study protocol for a randomized controlled trial of a universal group-based parenting support program. BMC Public Health. 2015 Apr 21;15:409. doi: 10.1186/s12889-015-1732-3.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- FIV1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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