NCT06828302

Brief Summary

The goal of this feasibility study is to evaluate feasibility of Internet-delivered Parent-Child Interaction Therapy for parents of children 2-7 years with disruptive behaviors. The main questions it aims to answer are:

  1. 1.Could a brief online version of PCIT (iPCIT) be feasible for reducing disruptive behaviors and internalizing problems in young children, and for improving the quality of parent-child interaction?
  2. 2.How is iPCIT experienced by participating parents?

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
1mo left

Started Mar 2025

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress92%
Mar 2025Jun 2026

First Submitted

Initial submission to the registry

February 10, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

February 14, 2025

Completed
24 days until next milestone

Study Start

First participant enrolled

March 10, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2025

Completed
9 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2026

Expected
Last Updated

December 8, 2025

Status Verified

October 1, 2025

Enrollment Period

7 months

First QC Date

February 10, 2025

Last Update Submit

December 1, 2025

Conditions

Keywords

Internet-CBTParentChildrenParent-Child Interaction Therapy

Outcome Measures

Primary Outcomes (1)

  • Eyberg Child Behavior Inventory

    Caregiver report form measuring disruptive behaviors in children. 36 items with answers ranging from 1 (never) to 7 (always). Minimum value: 36. Maximum value: 252. A higher score means worse outcome.

    From pretreatment to 18 weeks

Secondary Outcomes (8)

  • Weekly assessment of Child Behavior Forms

    From pretreatment to 18 weeks

  • Child Behavior Checklist

    From pretreatment to 10 weeks

  • Dyadic Parent-Child Interaction Coding System

    From pretreatment to 10 weeks

  • Brunnsviken Brief Quality of Life Scale

    From pretreatment to 18 weeks

  • Perceived Stress Scale

    From pretreatment to 18 weeks

  • +3 more secondary outcomes

Other Outcomes (5)

  • Working Alliance Inventory

    Treatment week 3

  • Credibility Rating Scale

    Treatment week 3

  • The Client Satisfaction Questionnaire

    Posstreatment (treatment week 10)

  • +2 more other outcomes

Study Arms (1)

iPCIT

OTHER

Online parent management training (PMT) to teach parental skills (10 weekly online modules) combined with videosession for coaching of parental skills (5 biweekly sessions)

Behavioral: Internet-delivered Parent-Child Interaction Therapy

Interventions

Parent management training delivered online where Internet-modules are combined with video sessions for live coaching.

Also known as: Internet-CBT, Internet-delivered cognitive behavior therapy
iPCIT

Eligibility Criteria

Age2 Years - 7 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Children aged 2-7 years
  • Disruptive behaviors as assessed with Eyberg Child Behavior Inventory (ECBI) ≥126 for boys and ≥121 for girls (which corresponds to the 90th percentile according to Swedish norms)
  • Language ability equivalent to at least an average 2-year-old, defined as a vocabulary of ≥ 25 word and ability to understand simple instructions, assessed with a language screening form

You may not qualify if:

  • Severe autism spectrum condition (autism level 2 or 3 or equivalent functioning)
  • parents who are not proficient enough in the Swedish language to complete questionnaries and receive therapy without an interpreter
  • Presence of severe parental psychiatric disorders such as psychosis or suicidal ideations
  • Ongoing severe psychosocial distress such as custody dispute.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centre for Psychiatry Research, Karolinska Institutet

Stockholm, Sweden

Location

MeSH Terms

Conditions

Problem Behavior

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorChild Behavior

Study Officials

  • Marianne Bonnert, PhD

    Centre for Psychiatry Research, Karolinska Institutet & Stockholm Health Care Stockholm Sweden

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
Self-reported outcomes assessed online without any influence from study staff.
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: Uncontrolled feasibility study using pretest-posttest design with 2 mo FU as primary endpoint.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD, lic psych, principal investigator

Study Record Dates

First Submitted

February 10, 2025

First Posted

February 14, 2025

Study Start

March 10, 2025

Primary Completion

September 30, 2025

Study Completion (Estimated)

June 15, 2026

Last Updated

December 8, 2025

Record last verified: 2025-10

Locations