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随机对照试验评估针对肥胖风险幼儿的虚拟育儿干预:多伦多育儿干预与教练访视(PARENT)试验的研究方案。

Randomized controlled trial evaluating a virtual parenting intervention for young children at risk of obesity: study protocol for Parenting Addressing Early Years Intervention with Coaching Visits in Toronto (PARENT) trial.

机构信息

Department of Nutritional Sciences, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

Child Health Evaluative Sciences, The Peter Gilgan Centre for Research and Learning, The Hospital for Sick Children, Toronto, ON, Canada.

出版信息

Trials. 2023 Jan 4;24(1):8. doi: 10.1186/s13063-022-06947-w.

Abstract

BACKGROUND

The prevalence of overweight (15%) and obesity (6%) in children under 5 years of age in Canada are high, and young children with overweight and obesity are at increased risk of the development of chronic disease(s) in adulthood. Prior research has demonstrated very few published trials on effective obesity prevention interventions in young children at risk of obesity, within primary healthcare settings. The aim of this study is to determine if 18-48-month-old children at risk for obesity, who are randomized to receive the Parents Together program (i.e., intervention group), have reduced body mass index z-score (zBMI), compared to those not receiving the intervention, at a 12-month follow-up. Secondary clinical outcomes between the intervention and control groups will be compared at 12 months.

METHODS

A pragmatic, parallel group, 1:1, superiority, randomized control trial (RCT) through the TARGetKids! Practice Based Research Network will be conducted. Young children (ages 18-48 months) who are at increased risk for childhood obesity will be invited to participate. Parents who are enrolled in the intervention group will participate in eight weekly group sessions and 4-5 coaching visits, facilitated by a trained public health nurse. Children and parents who are enrolled in the control group will receive the usual health care. The primary outcome will be compared between intervention arms using an analysis of covariance (ANCOVA). Feasibility and acceptability will be assessed by parent focus groups and interviews, and fidelity to the intervention will be measured using nurse-completed checklists. A cost-effectiveness analysis (CEA) will be conducted.

DISCUSSION

This study will aim to reflect the social, cultural, and geographic diversity of children in primary care in Toronto, Ontario, represented by an innovative collaboration among applied child health researchers, community health researchers, and primary care providers (i.e., pediatricians and family physicians in three different models of primary care). Clinical and implementation outcomes will be used to inform future research to test this intervention in a larger number, and diverse practices across diverse geographic settings in Ontario.

TRIAL REGISTRATION

ClinicalTrials.gov NCT03219697. Registered on June 27, 2017.

摘要

背景

加拿大 5 岁以下儿童超重(15%)和肥胖(6%)的患病率较高,超重和肥胖的幼儿成年后患慢性疾病的风险增加。先前的研究表明,在初级保健环境中,针对有肥胖风险的幼儿的有效肥胖预防干预措施,发表的试验很少。本研究旨在确定在为期 12 个月的随访中,接受父母一起计划(即干预组)的有肥胖风险的 18-48 个月大的儿童,与未接受干预的儿童相比,其体重指数 z 分数(zBMI)是否降低。在 12 个月时,将比较干预组和对照组之间的次要临床结果。

方法

通过 TARGetKids!实践为基础的研究网络,将开展一项实用的、平行组、1:1、优势、随机对照试验(RCT)。将邀请有儿童肥胖风险的幼儿参与。参加干预组的父母将参加八周的小组会议和 4-5 次教练访问,由一名经过培训的公共卫生护士协助。参加对照组的儿童和父母将接受常规医疗保健。将使用协方差分析(ANCOVA)比较干预组之间的主要结果。将通过家长焦点小组和访谈评估可行性和可接受性,并使用护士填写的检查表测量对干预的保真度。将进行成本效益分析(CEA)。

讨论

本研究旨在反映多伦多安大略省初级保健中儿童的社会、文化和地理多样性,这是通过应用儿童健康研究人员、社区健康研究人员和初级保健提供者(即三种不同模式的儿科医生和家庭医生)之间的创新合作实现的。临床和实施结果将用于为未来的研究提供信息,以在安大略省更多不同地理环境的不同实践中测试该干预措施。

试验注册

ClinicalTrials.gov NCT03219697。注册于 2017 年 6 月 27 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4367/9811774/cacd77f45dbb/13063_2022_6947_Fig1_HTML.jpg

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