The Effectiveness of Parent Training as a Treatment for Preschool Attention-Deficit/Hyperactivity Disorder: Study Protocol for a Randomized Controlled, Multicenter Trial of the New Forest Parenting Program in Everyday Clinical Practice

Autor: Anne-Mette Lange, Morten Frydenberg, Per Hove Thomsen, Edmund J.S. Sonuga-Barke, Charlotte Ulrikka Rask, David Daley
Rok vydání: 2015
Předmět:
Psychological intervention
Social Sciences
ADULT ADHD
clinical
law.invention
psycho-social
non-pharmacological
0302 clinical medicine
DIFFICULTIES QUESTIONNAIRE
Randomized controlled trial
law
Medicine and Health Sciences
Child and adolescent psychiatry
Clinical endpoint
Protocol
TEACHER RATINGS
GENERAL-POPULATION
child
treatment
treatment as usual
PSYCHIATRIC-DISORDERS
05 social sciences
parents
General Medicine
Multi-centre study
Psychology
RCT
INTERVENTIONS
050104 developmental & child psychology
Clinical psychology
medicine.medical_specialty
DEFICIT HYPERACTIVITY DISORDER
preschool
REPORT SCALE ASRS
03 medical and health sciences
Multicenter trial
medicine
Attention deficit hyperactivity disorder
ADHD
CHILDRENS ADHD
0501 psychology and cognitive sciences
Consolidated Standards of Reporting Trials
medicine.disease
RCT
clinical

parent training
Parent training
COMMUNITY SAMPLE
multi-centre
psychological
TAU
030217 neurology & neurosurgery
Zdroj: JMIR Research Protocols
JMIR RESEARCH PROTOCOLS
Lange, A-M, Daley, D, Frydenberg, M, Rask, C U, Sonuga-Barke, E & Thomsen, P H 2016, ' The Effectiveness of Parent Training as a Treatment for Preschool Attention-Deficit/Hyperactivity Disorder : Study Protocol for a Randomized Controlled, Multicenter Trial of the New Forest Parenting Program in Everyday Clinical Practice ', JMIR research protocols, vol. 5, no. 2, e51 . https://doi.org/10.2196/resprot.5319
ISSN: 1929-0748
Popis: Background: Parent training is recommended as the first-line treatment for attention-deficit/hyperactivity disorder (ADHD) in preschool children. The New Forest Parenting Programme (NFPP) is an evidence-based parenting program developed specifically to target preschool ADHD.Objective: The objective of this trial is to investigate whether the NFPP can be effectively delivered for children referred through official community pathways in everyday clinical practice.Methods: A multicenter randomized controlled parallel arm trial design is employed. There are two treatment arms, NFPP and treatment as usual. NFPP consists of eight individually delivered parenting sessions, where the child attends during three of the sessions. Outcomes are examined at three time points (T1, T2, T3): T1 (baseline), T2 (week 12, post intervention), and T3 (6 month follow/up). 140 children between the ages of 3-7, with a clinical diagnosis of ADHD, informed by the Development and Well Being Assessment, and recruited from three child and adolescent psychiatry departments in Denmark will take part. Randomization is on a 1:1 basis, stratified for age and gender.Results: The primary endpoint is change in ADHD symptoms as measured by the Preschool ADHD-Rating Scale (ADHD-RS) by T2. Secondary outcome measures include: effects on this measure at T3 and T2 and T3 measures of teacher reported Preschool ADHD-RS scores, parent and teacher rated scores on the Strength & Difficulties Questionnaire, direct observation of ADHD behaviors during Child’s Solo Play, observation of parent-child interaction, parent sense of competence, and family stress. Results will be reported using the standards set out in the Consolidated Standards of Reporting Trials Statement for Randomized Controlled Trials of nonpharmacological treatments.Conclusions: The trial will provide evidence as to whether NFPP is a more effective treatment for preschool ADHD than the treatment usually offered in everyday clinical practice.Trial Registration: ClinicalTrials.gov NCT01684644; https://clinicaltrials.gov/ct2/show/NCT01684644?term= NCT01684644&rank=1
Databáze: OpenAIRE