The Effect and Experience of the Parental Program AFFEKT

NCT05983705 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 198

Last updated 2026-04-16

No results posted yet for this study

Summary

This project is the first to evaluate the effect and experience of the parent program AFFEKT, through a randomized controlled trial and qualitative study, within primary health care. The project will recruit 200 parents of children with externalizing behaviors, and evaluate the effect of AFFEKT and psychoeducation versus psychoeducation alone, on children's behaviors and mental health, and the parent's strategies and mental health. Through interviews the experience of AFFEKT will be investigated.

Conditions

  • Behavior, Child
  • Parenting
  • Parent-Child Relations
  • Stress
  • Quality of Life

Interventions

BEHAVIORAL

AFFEKT - a manual based brief parent program for parents of children (aged 6-12 years) with externalizing behaviors.

The AFFEKT program includes five group sessions, two hours each, provided on a weekly basis. The program is delivered by therapist trained in Cognitive and Behavioral Therapy (CBT) and AFFEKT. The participants also receive a participation material, covering the same themes that are addressed in the program and working sheets for the home-assignments that are provided in-between sessions.

Sponsors & Collaborators

  • Medtanken Group AB

    collaborator OTHER
  • FoU i Västra Götalandsregionen

    collaborator UNKNOWN
  • Forte

    collaborator INDUSTRY
  • Göteborg University

    lead OTHER

Principal Investigators

  • Py Eriksson, Dr · Gothenburg University, Institute of Psychology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-23
Primary Completion
2025-10-30
Completion
2025-10-30

Countries

  • Sweden

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05983705 on ClinicalTrials.gov