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家长培训作为治疗学龄前注意力缺陷/多动障碍的有效性:新森林育儿计划在日常临床实践中的随机对照多中心试验研究方案

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.

作者信息

Lange Anne-Mette, Daley David, Frydenberg Morten, Rask Charlotte U, Sonuga-Barke Edmund, Thomsen Per H

机构信息

Centre for Child & Adolescent Psychiatry, Research Department, Aarhus University Hospital, Risskov, Denmark.

出版信息

JMIR Res Protoc. 2016 Apr 13;5(2):e51. doi: 10.2196/resprot.5319.

Abstract

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 (Archived by WebCite at http://www.webcitation/6eOOAe8Qe).

摘要

背景

家长培训被推荐为学龄前儿童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)是一项基于证据的育儿计划,专门针对学龄前ADHD儿童制定。

目的

本试验的目的是调查在日常临床实践中,通过官方社区途径转诊的儿童,NFPP是否能有效实施。

方法

采用多中心随机对照平行组试验设计。有两个治疗组,即NFPP组和常规治疗组。NFPP包括八个单独进行的育儿课程,孩子要参加其中三个课程。在三个时间点(T1、T2、T3)进行结果检查:T1(基线)、T2(干预后第12周)和T3(6个月随访)。140名年龄在3至7岁之间、经发育与幸福感评估确诊为ADHD的儿童将参与试验,他们从丹麦的三个儿童和青少年精神科招募。随机分组按1:1进行,按年龄和性别分层。

结果

主要终点是在T2时通过学龄前ADHD评定量表(ADHD-RS)测量的ADHD症状变化。次要结果指标包括:T3时该指标的效果以及T2和T3时教师报告的学龄前ADHD-RS分数、家长和教师在优势与困难问卷上的评分、在孩子独自玩耍期间对ADHD行为的直接观察、亲子互动观察、家长的能力感以及家庭压力。结果将按照非药物治疗随机对照试验的《报告试验的统一标准》中规定的标准进行报告。

结论

该试验将提供证据,证明NFPP对学龄前ADHD的治疗是否比日常临床实践中通常提供 的治疗更有效。

试验注册

ClinicalTrials.gov NCT01684644;https://clinicaltrials.gov/ct2/show/NCT01684644?term= NCT01684644&rank=1(由WebCite存档于http://www.webcitation/6eOOAe8Qe)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7195/4848388/81674d488e17/resprot_v5i2e51_fig1.jpg

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