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RecruitingNCT05686473NorFASDPEduUpdated May 21, 2025

Psychoeducation of Parents to Children With FASD

An interventional study of Program of psychoeducation of parents and professionals in Fetal Alcohol Spectrum Disorders, Behavior Problem and Adaptive Behavior, sponsored by Sorlandet Hospital HF. Recruiting at 1 site in Norway. Open to participants aged 2 Years to 18 Years. Per ClinicalTrials.gov, last updated 2025-05-21.

Sponsored by Sorlandet Hospital HF · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Started May 2025; still recruiting 1 year 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
75
Allocation
Not applicable
Ages
2 Years to 18 Years
Sex
All
01

Study summary

By longitudinal, prospective research in children and adolescents with Fetal Alcohol Spectrum Disorders (FASD) and their parents to explore the beneficial effects of participating in a standardized intervention program in order to treat and reduce the consequences of early brain damage. By using elements from international programs based on psychoeducation and parent training, the investigators aim to help parents to better understand and respond to the neurodevelopmental disabilities of their children, and thereby improving behavioral problems and self-regulation deficits.

Read the detailed description

The main aim of this research project is to evaluate the effects of a standardized intervention program for parents and professionals working with children and adolescents with FASD. Focus will be on care-persons' knowledge and skills and psychoeducation with regard to improved handling of behavioral problems and deficits in self-regulation due to FASD.

To achieve this aim objectives will be:

  • to collect and analyse data on family empowerment, parenting skills and stress before and after participation in the intervention program.
  • to collect and analyse data on the child's behavior and deficits in self-regulation before and after participation in the intervention program.
  • to collect and analyse data on professionals' knowledge of FASD before and after participation in the intervention program.

The current study hypothesizes that caregivers who understand and view their children's behavior from a neurodevelopmental perspective are more likely to feel competence, use antecedent strategies, and thereby reduce child problem behavior and improve functional outcome (Fig. 2). The investigators hypothesize that participation in this program will improve parental empowerment and child self-regulation and behavior compared with baseline assessments.

02

Conditions studied

  • Fetal Alcohol Spectrum Disorders
  • Behavior Problem
  • Adaptive Behavior
  • Learning Disorders

Keywords

  • FASD
  • Psychoeducation
  • Parenting
  • Information program
03

In context

Fetal Alcohol Spectrum Disorders

65 studies on the registry are indexed under Fetal Alcohol Spectrum Disorders; 13 are open to participants now.

This study's planned enrollment of 75 is close to the median of 74 across 57 interventional studies indexed under Fetal Alcohol Spectrum Disorders.

Browse Fetal Alcohol Spectrum Disorders studies →

Lead sponsor

Sorlandet Hospital HF is the lead sponsor of 74 studies on the registry; 12 are open to participants now.

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

04

Who can participate

Ages eligible
2 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

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.

All children and adolescents (age 2,5-18 years) referred to the Regional Competence Centre for children with prenatal alcohol exposure in Arendal, Norway will be invited to participate in the current research project.

Inclusion criteria

Inclusion criteria:

  • Valid information about alcohol exposure in fetal life. Exceptions to this inclusion criterion are children who have been adopted and with dysmorphic features that are consistent with full Fetal Alcohol Syndrome.

Exclusion criteria

Exclusion Criteria:

  • Children with known genetic syndromes, progressive brain and neuromuscular diseases or major sensory defects (blindness or deafness).
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
75 participants (estimated)

Study arms

  • Experimental
    Patient group

    Single arm study. The family with child with FASD will act as its own control in the period before intervention starts.

    Behavioral: Program of psychoeducation of parents and professionals

Interventions

  • BehavioralProgram of psychoeducation of parents and professionals

    The program consists of a standardized manual-based treatment package as an easily accessible treatment tool for use by professionals in the specialist health services, who have treatment responsibilities for children diagnosed with FASD in Norway. The intervention program will last for about 2 months and includes eight sessions, including six digitally based, interactive psychoeducational sessions. Topics will be: 1. General information about FASD 2. Intervention strategies in kindergartens/schools for children with FASD 3. Families living with FASD - activities of daily living 4. Self-regulatory deficits - how to cope 5. Executive functions in daily life 6. Social development in children with FASD 7. Guidance in social settings 8. Challenging behavior - what can be done

06

What researchers measure

Primary outcomes

  1. The Children's Global Assessment Scale (CGAS)

    To evaluate effects of the intervention program well-known standardized, validated measures will be used. Primary outcome measure for the child will be The Children's Global Assessment Scale, which is a numeric scale used by mental health clinicians to rate the general functioning of youths under the age of 18. The scale targets the number of behavioral problems and the frequency of their occurrence.The child or young person is given a single score between 1 and 100. Higher score means better functioning.

    Time frame: up to 10 months

  2. The Family Empowerment Scale (FES)

    Primary outcome measure for parents will be The Family Empowerment Scale to evaluate the magnitude of empowerment in the parent-child system. FES is a 34-item rating scale where the participants rate each item on a 5-point Likert-type rating scale. Scores will range between 34 and 170 points. Increasing scores indicate a positive significance regarding family empowerment.

    Time frame: up to 10 months

Secondary outcomes

  1. The Eyberg Child Behavior Inventory (ECBI)

    In addition, several well-known secondary measures will be used to evaluate additional effects of program. The ECBI questionnaire will be used to evaluate the number of behavioral problems and the frequency of their occurrence before and after the intervention program. ECBI provides a list of 36 problem behaviors commonly reported by parents. The inventory assesses behavior on two dimensions: 1) the frequency of the behavior; 2) whether parents consider it a problem. The frequency ratings range from 1 (never) to 7 (always), and are summed up to arrive at an overall problem behavior Intensity Score, ranging from 36 to 252. Higher score means more behavioral problems.

    Time frame: up to 10 months

  2. The Social Responsiveness Scale, Second Edition (SRS-2)

    The SRS-2 questionnaire will be used to evaluate the severity of social impairment and lack of flexibility in children and adolescents before and after participation in the intervention program. Each domain's T-scores are organized by gender and respondent age, with each domain having varied but similar ranges of possible scores from 32 points-114 points. All T-scores have a mean of 50 points with a standard deviation of 10 points. Higher score means more deficits in social interaction.

    Time frame: up to 10 months

  3. The Behavior Rating Inventory of Executive Function, Second Edition (BRIEF-2)

    The BRIEF-2 will be used to evaluate any change in executive functions after participation. Norms tables give T-scores, percentiles, and 90% confidence intervals for four developmental age groups, by gender. Three broad indexes are calculated (Behavior Regulation, Emotion Regulation, and Cognitive Regulation). Higher score means worse outcome.

    Time frame: up to 10 months

  4. The Parenting Stress Index (PSI)

    The PSI questionnaire will be used to evaluate parental stress and load before and after participation in the program.The PSI yields a total score, three domain scores, and 15 subscales. Higher raw scores indicate higher levels of stress.

    Time frame: up to 10 months

07

Study locations

1 of 1 sites recruiting
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References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 21, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05686473
Lead sponsor
Sorlandet Hospital HF
Responsible party
Sponsor
First posted
Jan 17, 2023
Start date
May 1, 2025
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
May 21, 2025

Study contacts

Anne Cecilie Tveiten, PhD student
Contact
Anne.Cecilie.Tveiten@sshf.no
+47-370-75750
Gro CC Løhaugen, PhD
Contact
Gro.lohaugen@sshf.no
+47-370-75750
Jon S Skranes, Dr Med
principal investigator · Sørlandet Hospital HF

Oversight

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

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