- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06874998
Effects of "Parenting in Sweden" on Trust in Social Services (PiSRCT)
Effects of "Parenting in Sweden" on Trust in Social Services - a Randomized Controlled Trial
Supporting Parents in a New Country
Adjusting to parenthood in a new country presents significant challenges. Many immigrant parents face language barriers, financial difficulties, and cultural differences that can complicate their ability to support their children's adaptation to Swedish society. These challenges can contribute to increased stress within the family and, in some cases, elevate the risk of child maltreatment-particularly in socioeconomically disadvantaged areas. However, research suggests that strong social support and positive parenting strategies can mitigate these risks.
Sweden, known for its high levels of trust in authorities, has implemented various initiatives to assist families, especially those new to the country. One such initiative is Parenting in Sweden (PiS), a structured program designed to help foreign-born parents navigate Swedish society, understand their rights, and support their children's development. Delivered in five sessions, the program covers key topics such as the Swedish school system, healthcare services, parental rights, and challenges related to raising teenagers.
This study aims to assess whether participation in PiS increase parents' trust in social services. Additionally, it explores whether the program encourages parents to enroll their children in extracurricular activities, which are known to support child development. Another important aspect under investigation is whether the program can help reduce the risk of parents resorting to harsh disciplinary practices.
To evaluate these outcomes, the study follows a randomized controlled trial (RCT) design. Immigrant parents of children aged 0-17 are invited to participate, with half assigned to complete the full five-session program and the other half (control group) placed on a waiting list, receiving a group meeting to discuss films related to moving to Sweden. All participants will complete surveys assessing their trust in social services, their children's participation in extracurricular activities, and their parenting practices. These surveys will be administered before and after the program, as well as six months later, to track any changes over time.
The primary objective is to determine whether participation in PiS leads to increased trust in social services. Additional expected benefits (exploratory analysis) include promoting positive parenting behaviors, such as seeking help when needed and actively engaging children in structured activities outside of school.
By examining the effectiveness of parental support programs facilitating integration, this study aims to contribute to a deeper understanding of how structured interventions can help families navigate life in Sweden. If the program proves successful in fostering trust and encouraging positive parenting, it may have long-term benefits for both parents and children, ultimately supporting their well-being and integration into Swedish society.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Anna MS Dahl, Medical Doctor
- Phone Number: +46735350411
- Email: anna_dahl@live.se
Study Contact Backup
- Name: David Ebbevi, Md, PhD
- Phone Number: +468-12383373
- Email: david.ebbevi@ki.se
Study Locations
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Stockholm, Sweden
- Stockholm - distibuted
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- All parents invited to participate in PiS can take part in the study.
- Eligibility extends to parents born outside of Sweden who have children aged 0 to 17 years.
- There are no restrictions regarding the length of time since their migration to Sweden; i.e., participants may have lived in Sweden for decades prior to joining. - - Literacy is not a requirement for participation.
Exclusion Criteria:
- Individuals who are unable, physically or not willing, to sign a consent form will not be eligible to participate in the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Parenting in Sweden
The intervention group will be given the full program straight after recruitment ("Structured group discussions").
The program consists of five 3-hour sessions once a week.
The themes for the five sessions are: Family in a new country, School, girls and boys, Health and health care system, Parents rights and obligations and parenting a teenager.
Each session combines lectures and group discussions on topics critical to families adapting to life in Sweden.
The sessions are held by a trained group leader and, if needed, interpreters.
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A group-based program for immigrant parents of children aged 0-17, providing essential information on key aspects of family life in Sweden. The intervention consists of five weekly three-hour sessions, combining lectures, group discussions, and interactive exercises, led by a trained group leader and, when necessary, an interpreter. The following topics are discussed:
Other Names:
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Placebo Comparator: Waitlist
The control group will be placed on a waiting list for 6 months ("Unstructured group meeting").
After 6 weeks the control group is offered a session with two short films from the Swedish Educational Broadcasting Company (UR), followed by a brief discussion.
The first film explores how one can establish a place in society, the second film illustrates how hard it can be to create a new social context.
The intention with the short films is not to give a short version of PiS, but to engage parents in the study and the program so they will complete them.
The control group is then offered to participate in the whole program after 6 months.
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Parents in the control group are asked to participate in a gathering where they will watch two short films from the Swedish Educational Broadcasting Company (UR), followed by a brief discussion.
The films have been handpicked by representatives from BRIS and PLUS together with the researchers to create an opportunity for a meeting.
The first film "A way in - first meeting" shows a family from Iran living in Sweden for 1,5 years and explores how one can establish a place in society.
In the second film "Make new friends" it is illustrated how hard it can be to create a new social context.
The intention with the short films is not to give a short version of PiS, but to engage parents in the study and the program so they will complete them.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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What are the effects of PiS on the level of trust in social services among parents born outside of Sweden?
Time Frame: From enrollment to 6 months after.
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The research question will be assessed through the question, "Overall, to what extent do you trust that those who work in Social services (SS) do their job?" ranked on a 5-point Likert scale.
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From enrollment to 6 months after.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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How valid and reliable is an adapted government trust scale for measuring trust in social services?
Time Frame: From enrollment to 6 months after.
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By using an adjusted version of a validated scale for the measure of trust in government, trust in social services will be assessed. The instrument measures on a 5-point Likert scale. English translation:
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From enrollment to 6 months after.
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Does participating in PiS increase enrollment of children in organized after-school activities
Time Frame: The question is asked in the baseline survey at enrollment and asked again at the 6-month follow-up.
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The number of children attending organized after-school activities will be measured through a forced-choice question: Do your children attend any organized after-school activities?
If the answer is no, parents are given a number of options to tick .
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The question is asked in the baseline survey at enrollment and asked again at the 6-month follow-up.
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Does participating in PiS decrease risk factors of child maltreatment?
Time Frame: From enrollment to 6 months after.
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Risk factors for use of child abuse will be assessed through a validated questionnaire, Brief Child Abuse Potential Inventory (BCAP) developed by Ondersma et al.
BCAP is a shortened version of the screening tool for detecting potential child maltreatment, the Child Abuse Potential Inventory (CAPI).
The CAP Inventory is a self-report measure of 160 forced-choice (agree/disagree) questions.
But some characteristics, such as the length of the questionnaire and the complex scoring system, limit the screening tool's usefulness, which is why the shorter version was developed.
BCAP contains seven factors: Distress, Family Conflict, Rigidity, Happiness, Feelings of Persecution, Loneliness, and Financial Insecurity.
These factors are not used to produce individual factor scores but to ensure the Abuse Risk scale includes a range of dimensions associated with physical child abuse risk.
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From enrollment to 6 months after.
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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What are the mechanisms behind the effectiveness of the program?
Time Frame: From enrollment to 6 months after.
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To understand the mechanisms behind the effectiveness of the program and to perform exploratory subgroup analysis, group leaders will also provide information.
Through a baseline questionnaire, they are asked about their age, gender, which languages they speak, their native country and when they moved to Sweden if applicable, their highest education, their occupation, how many Parenting in Sweden groups they have led or if they have led any other groups in parental support programs, and how they assess their own knowledge regarding social services.
They will also supply information through a self-assessment form regarding their leadership abilities, the content of the session, and parent engagement after every session.
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From enrollment to 6 months after.
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2024-06868-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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