Psychoeducation program for parents of children with Fetal Alcohol Spectrum Disorders
Evaluation of a Treatment Program Based on Psychoeducation of Parents of Children and Adolescents With Fetal Alcohol Spectrum Disorder (FASD)
This study is testing a program to help parents of kids with Fetal Alcohol Spectrum Disorders learn better ways to manage their children's behavior and improve family life.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 75 (estimated) |
| Ages | 2 Years to 18 Years |
| Sex | All |
| Sponsor | Sorlandet Hospital HF Government |
| Locations | 1 site (Arendal) |
| Trial ID | NCT05686473 on ClinicalTrials.gov |
What this trial studies
This research evaluates the effects of a standardized psychoeducation intervention program aimed at parents and professionals working with children and adolescents diagnosed with Fetal Alcohol Spectrum Disorders (FASD). The program focuses on enhancing caregivers' knowledge and skills to better manage behavioral problems and self-regulation deficits associated with FASD. Data will be collected on family empowerment, parenting skills, and child behavior before and after participation in the program to assess its effectiveness. The study hypothesizes that improved understanding of neurodevelopmental issues will lead to better outcomes for both parents and children.
Who should consider this trial
Good fit: Ideal candidates for this study are children and adolescents aged 2.5 to 18 years with a confirmed history of prenatal alcohol exposure.
Not a fit: Patients with known genetic syndromes, progressive brain diseases, or major sensory defects may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly improve parenting skills and child behavior in families affected by FASD.
How similar studies have performed: Other studies have shown positive outcomes with psychoeducational interventions for similar conditions, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
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: * 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: * Children with known genetic syndromes, progressive brain and neuromuscular diseases or major sensory defects (blindness or deafness).
Where this trial is running
Arendal
- Sørlandet Hospital — Arendal, Norway (Recruiting)
Study contacts
- Principal investigator: Jon S Skranes, Dr Med — Sørlandet Hospital HF
- Study coordinator: Anne Cecilie Tveiten, PhD student
- Email: Anne.Cecilie.Tveiten@sshf.no
- Phone: +47-370-75750
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.