Effectiveness of a Foster Parent Intervention: Results of a Trial

NCT ID: NCT01821755

Last Updated: 2013-04-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

63 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-01-31

Study Completion Date

2013-05-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The hypothesis of the study is that the intervention leads to a reduction in foster children's externalizing problems and foster parents' parenting stress and that this in turn leads to a reduction in the number of breakdowns of foster placements.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Problematic Behavior in Children Parent-child Problem

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Behavioral: Foster parent intervention

Foster parents receive a foster parent intervention consisting of 10 individual home visits and three group sessions. Duration of the intervention is four months

Group Type EXPERIMENTAL

Foster parent intervention

Intervention Type BEHAVIORAL

parent management training for foster parents, consisting of 10 individual home visits and 3 group sessions. Duration is four months

Control

waiting-list control group who receive care-as-usual

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Foster parent intervention

parent management training for foster parents, consisting of 10 individual home visits and 3 group sessions. Duration is four months

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* foster child has a borderline or clinical score on one of the small-band externalizing scales or the broad-band externalizing scale of the Child Behavior Checklist (CBCL)

Exclusion Criteria

foster child:

* has a mental retardation,
* autism,
* uses psychotropic medication in an inconsistent way,
* behavioral problems are the result of medical problems or medication, foster parents:
* have insufficient knowledge of Dutch,
* have low cognitive abilities,
* are already receiving professional support for the foster child's externalizing problems,
* are divorcing.

Moreover, foster placements were excluded if at least two of the following criteria were present:

* foster parents considered terminating the foster placement during the past two months
* were experiencing psychological distress (measured with the General Health Questionnaire (GHQ; Koeter \& Ormel, 1991) and defined as a score ≥ 2),
* their foster child had a sum score above 3 (for children \< 6 years) or 5 (for children ≥ 6 years) on the critical CBCL-items.
Minimum Eligible Age

3 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Vrije Universiteit Brussel

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Femke vanschoonlandt

PhD Student

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Vrije Universiteit Brussel

Brussels, Vlaams-Brabant, Belgium

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Belgium

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

ID0032

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Trial of Transition to Parenthood Program for Couples
NCT01907412 ACTIVE_NOT_RECRUITING NA
Holding a Foster Child's Mind in Mind
NCT05196724 ACTIVE_NOT_RECRUITING NA
Promoting Infant Mental Health in Foster Care
NCT00339365 COMPLETED PHASE2/PHASE3
Intervening Early With Neglected Children
NCT02093052 UNKNOWN PHASE1/PHASE2