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Enrolling by invitationNCT04519229Updated Aug 12, 2026

Child-Parent Psychotherapy - a Feasibility Study for Children in Foster Care

An observational study in Child Abuse, Child Neglect and Post-Traumatic Stress Disorder in Children, sponsored by Kronoberg County Council. Enrolling by invitation at 1 site in Sweden. Open to participants aged 0 Years to 6 Years. Per ClinicalTrials.gov, last updated 2026-08-12.

Sponsored by Kronoberg County Council · Observational

Study type
Observational
Model
Ecologic or community
Time perspective
Prospective
Enrollment
20
Ages
0 Years to 6 Years
Sex
All
01

Study summary

Children in foster care have an increased risk of exposure to adverse experiences during childhood and across the lifespan. In current studies of interventions children in foster care are often excluded, or they are too few to be included in statistical analyses of outcomes. As a consequence, knowledge on feasibility of treatment methods for some of the most exposed and maltreated children in society is sparse.

Child-Parent Psychotherapy (CPP) is an intervention for children 0-6 years who have been exposed to adverse and traumatic events. CPP is currently being implemented in Sweden. The aim of this study is to investigate the feasibility of CPP for children in foster care.

Read the detailed description

Aim. The aim of the current study is to investigate the feasibility of CPP for young children who have an increased risk of exposure to adverse and traumatic experiences with negative effects on their health and development. Feasibility will be conceptualized as acceptance of the method by therapists, caregivers, and children; practical applications of the method; any need for modifications; and observed outcomes.

Research questions The main research question is: Is CPP feasible for children in foster care? Additional research questions are: 1) How do children in foster care experience participating in CPP? 2) How do foster parents experience participating in CPP? 3) How do clinicians experience using CPP with children in foster care and their caregivers? 4) What outcomes can be observed in treatment with children in foster care in terms of increased psychological health in children and foster parents; decrease in symptoms of post-traumatic stress in children and foster parents; and foster parents' experiences of their caregiving capacity and relationship with the child.

Method Design. The project has a naturalistic mixed-methods study design. Qualitative and quantitative research methods will be used to collect and analyze data. Qualitative data concerning childrens', caregivers', and clinicians' experiences of the treatment method as well as quantitative data concerning practical applications of the method, any modifications made, and reported levels of symptoms will be studied.

Participants. Nine agencies in different regions of Sweden offering CPP as part of their regular services have accepted to participate in the study. Participants are consecutively recruited at the participating agencies. Inclusion will be terminated when 20 children have been included (whereof at least 12 children aged 3-6 years).

Procedure. At treatment start caregivers and custodians (this can include foster parents, social services, and biological parents) will be informed about the study and asked for consent to participate. Because of their low age children aged 3-6 will be informed and asked for consent to participate in connection to the interviews. Quantitative data will be collected by self-report instruments completed by the foster parents before treatment and after 20 sessions or at termination, if treatment if terminated earlier. Participation, fidelity, and modifications are registered by clinicians continuously. Foster parents and clinicians will be asked to schedule interviews by one of the researchers in the project after 20 sessions or at termination, if treatment if terminated earlier.

Background information. Demographical and background data will be collected using a form designed for this purpose, before treatment and after 20 sessions or at termination, if treatment is terminated earlier.

Instrument. Qualitative interviews focusing acceptance and experiences of the method will be conducted with children, foster parents, and clinicians. The interviews will be conducted by child psychologists experienced in clinical treatment as well as in research with families with young children in in difficult life situations. The interviews will be recorded and transcribed verbatim. Clinicians will register participation, fidelity, and any modifications after each treatment session in a log-book. Quantitative data on outcome concerning exposure, symptoms of post-traumatic stress, psychological health, and caregiving experiences will be collected by self-report instruments completed by foster parents before treatment and after 20 sessions or at termination, if treatment is terminated earlier.

Analyses. The interviews will be analyzed by thematic analysis or interpretative phenomenological analysis, according to the applicability in relation to the research questions and data collected. Descriptive statistical methods will be used to describe exposure, symptoms pre- and post-treatment, and treatment modifications made. Non-parametric statistical methods will be used to analyze and describe indications concerning outcome.

02

Conditions studied

  • Child Abuse
  • Child Neglect
  • Post-Traumatic Stress Disorder in Children
  • Parent-Child Relations

Keywords

  • Children
  • Adverse childhood events
  • Post traumatic stress
  • Children in foster care
  • Psychotherapy
03

In context

Stress Disorders, Post-Traumatic

2,682 studies on the registry are indexed under Stress Disorders, Post-Traumatic; 601 are open to participants now.

This study's planned enrollment of 20 is below the median of 150 across 371 observational studies indexed under Stress Disorders, Post-Traumatic.

Browse Stress Disorders, Post-Traumatic studies →

Lead sponsor

Kronoberg County Council is the lead sponsor of 13 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
0 Years to 6 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Children in foster care offered Child-Parent Psychotherapy at any of the nine participating agencies.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 0-6 years
  • being offered Child-Parent Psychotherapy as part of their regular treatment

Exclusion criteria

Exclusion Criteria:

  • Families in need of translator for interviews.
05

Study design

Observational model
Ecologic or community
Time perspective
Prospective
Enrollment
20 participants (estimated)
Patient registry
No

Groups and cohorts

  • Children in fostercare in CPP-treatment

    Children in foster care taking part in Child-Parent Psychotherapy

    Behavioral: Child-Parent Psychotherapy

Interventions

  • BehavioralChild-Parent Psychotherapy

    Relationship-based trauma focused psychotherapy for Children 0-6 years old and their caregivers. The objective is to decrease symptoms of post-traumatic tress and re-establish a secure attachment for the child and good caregiving from the caregiver/s.

06

What researchers measure

Primary outcomes

  1. Change from baseline score on the Strengths and Difficulties Questionnaire - Parent version at 20 completed sessions or at termination of intervention if terminated earlier.

    Caregiver report of child psychopathology. Minimum score 0, maximum score 40, higher score indicating worse outcome.

    Time frame: After 20 completed sessions or immediately after termination of the intervention, if terminated earlier than 20 sessions

  2. Change from baseline score on the Trauma Symptom Checklist for Young Children at 20 completed sessions or at termination of intervention if terminated earlier.

    Caregiver report of child symptoms of post-traumatic stress. Minimum score 90, maximum score 360, higher score indicating worse outcome.

    Time frame: After 20 completed sessions or immediately after termination of the intervention, if terminated earlier than 20 sessions

  3. Change from baseline score on the Linköping Youth Life Experiences Scale at 20 completed sessions or at termination of intervention if terminated earlier.

    Caregiver report of child exposure to traumatic and adverse life events. Minimum score 0, maximum score 41, higher score indicating worse outcome.

    Time frame: After 20 completed sessions or immediately after termination of the intervention, if terminated earlier than 20 sessions

  4. Change from baseline score on the Child-Parent Psychotherapy Symptom Screener at 20 completed sessions or at termination of intervention if terminated earlier.

    Caregiver report of child symptoms of post-traumatic reactions. Minimum score 0, maximum score 93, higher score indicating worse outcome.

    Time frame: After 20 completed sessions or immediately after termination of the intervention, if terminated earlier than 20 sessions

Secondary outcomes

  1. Change from baseline score on the Hopkins Symptom Check List-25 at 20 completed sessions or at termination of intervention if terminated earlier.

    Caregiver report of psychological distress and symptoms. Minimum score 0, maximum score 100, higher score indicating worse outcome.

    Time frame: After 20 completed sessions or immediately after termination of the intervention, if terminated earlier than 20 sessions

  2. Change from baseline score on the Impact of Event Scale-Revised at 20 completed sessions or at termination of intervention if terminated earlier.

    Caregiver report of symptoms of post-traumatic stress. Minimum score 0, maximum score 80, higher score indicating worse outcome.

    Time frame: After 20 completed sessions or immediately after termination of the intervention, if terminated earlier than 20 sessions

  3. Change from baseline score on the Life Incidence of Traumatic Events Questionnaire at 20 completed sessions or at termination of intervention if terminated earlier.

    Caregiver report of exposure to traumatic and adverse life events. Minimum score 0, maximum score 41, higher score indicating worse outcome.

    Time frame: After 20 completed sessions or immediately after termination of the intervention, if terminated earlier than 20 sessions

  4. Change from baseline score on the Caregiving Helplessness Questionnaire at 20 completed sessions or at termination of intervention if terminated earlier.

    Caregiver report on caregiving experiences. Minimum score 18, maximum score 90, higher score indicating worse outcome.

    Time frame: After 20 completed sessions or immediately after termination of the intervention, if terminated earlier than 20 sessions

Other outcomes

  1. Adherence

    Log of clinicians' ratings of fidelity to the method of Child-Parent Psychotherapy and adaptions immediately after each session, up to 20 times

    Time frame: After 20 completed sessions or immediately after termination of the intervention if terminated earlier than 20 sessions

  2. Childrens' experiences of participating in Child-Parent Psychotherapy

    Qualitative data from interviews with children 3-6 years old

    Time frame: After 20 completed sessions or immediately after termination of the intervention if terminated earlier than 20 sessions

  3. Foster parents' experiences of participating in Child-Parent Psychotherapy

    Qualitative data from interviews with foster parents

    Time frame: After 20 completed sessions or immediately after termination of the intervention if terminated earlier than 20 sessions

  4. Clinicians' experiences of working with Child-Parent Psychotherapy with Children in foster care

    Qualitative data from interviews with clinicians

    Time frame: After 20 completed sessions or immediately after termination of the intervention if terminated earlier than 20 sessions

07

Study locations

1 site
  • Department of Research and Development, Region Kronoberg
    Vaxjo, 35112, Sweden
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jun 2019 (actual). Primary completion is estimated for Dec 2026, 90 months after the start.

Of 142 non-industry observational studies under Stress Disorders, Post-Traumatic, half reached primary completion within 34 months of starting (the median), counting those still running; a quarter within 13 and three quarters within 59. This study's planned 90 months is above that.

Counting every sponsor, half of 149 studies reached it within 34 months; a quarter within 14 and three quarters within 54.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 9, 2020
First posted
Aug 19, 2020
StartActual
Jun 30, 2019
Primary completionEst.
Dec 31, 2026
CompletionEst.
Dec 31, 2027
Last update
Aug 12, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04519229
Lead sponsor
Kronoberg County Council
Collaborators
Stiftelsen Allmänna Barnhuset
Responsible party
Sponsor
First posted
Aug 19, 2020
Start date
Jun 30, 2019
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Aug 12, 2026

Study contacts

Karin Pernebo, PhD
study director · Department of Psychology, Linnaeus University, Sweden and Department of Research and Development, Region Kronoberg, Sweden

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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