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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

机译:父母培训作为学前教育注意力缺陷/多动障碍治疗的有效性:在日常临床实践中对新森林育儿计划进行随机对照,多中心试验的研究方案

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摘要

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
机译:背景:建议对学龄前儿童进行父母培训,作为注意力缺陷/多动障碍(ADHD)的一线治疗方法。新森林育儿计划(NFPP)是专门针对学龄前儿童多动症而开发的循证育儿计划。目的:该试验的目的是调查NFPP是否可以有效地提供给在日常临床实践中通过官方社区途径推荐的儿童方法:采用多中心随机控制的平行臂试验设计。有两个治疗分支,NFPP和常规治疗。 NFPP由八个单独分娩的育儿课程组成,孩子在三个课程中参加。在三个时间点(T1,T2,T3)检查结果:T1(基线),T2(干预后第12周)和T3(6个月随访/随访)。从发展和健康评估中获悉,并从丹麦的三个儿童和青少年精神病学部门招募的140名3到7岁的儿童具有多动症的临床诊断。结果:按年龄和性别分层,以1:1为基础。结果:主要终点是ADHD症状的变化,该变化通过T2的学前儿童ADHD评分量表(ADHD-RS)进行测量。次要结局指标包括:在教师报告的学前儿童ADHD-RS评分的T3,T2和T3度量上对该度量的影响,在“力量与困难问卷”中父母和教师的评分,直接观察儿童独奏时ADHD行为,对父母的观察互动,父母的能力和家庭压力。将使用《非药物治疗随机对照试验的试验报告合并标准声明》中规定的标准来报告结果。日常临床实践。试验注册:ClinicalTrials.gov NCT01684644; https://clinicaltrials.gov/ct2/show/NCT01684644?term= NCT01684644&rank = 1

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