跳至主要内容
临床试验/ACTRN12624001159549
ACTRN12624001159549进行中(未招募)Unknown

A cluster-randomised controlled trial examining the effectiveness of a multicomponent school-based systems intervention (TransformUs Wellbeing) on determinants of childhood obesity within Victorian primary schools.

Deakin University0 个研究点目标入组 759 人开始时间: 2024年9月24日最近更新:
适应症

试验速览

阶段
Unknown
状态
进行中(未招募)
入组人数
759
主要终点
Wellbeing[The 23-item Paediatric Quality of Life Inventory 4.0 (PedsQL)TM questionnaire will be used to examine perceived health-related quality of life among participants. Grade 4 and Grade 5 at baseline, and immediately post-intervention (approx. 9-months after baseline). ]

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention

入排标准

年龄范围
7 Years 至 13 Years(—)
性别
All

入选标准

  • All children in Grade 2, 3, 4 and 5 in participating primary schools in the Warrnambool, Corangamite and Moyne LGAs of South-West Victoria will be invited to participate in the monitoring component (n=35 schools).This trial is conducted in the real-world school setting. Entire schools are randomised to intervention or control and individual participants are not singled out. Inclusion criteria for the group model building workshop sessions will be based on facilitators judgement of the best placed school/community leaders/stakeholders who can generate community interest and buy-in for a community-led obesity prevention effort. There are no school-based inclusion criteria.

排除标准

  • There are no exclusion criteria for the monitoring component. All children in Grade 2, Grade 3, Grade 4 and Grade 5 at participating schools will be invited to participate.There are no exclusion criteria set for the group model building workshop sessions and or intervention school enrolment.

结局指标

主要结局

Wellbeing[The 23-item Paediatric Quality of Life Inventory 4.0 (PedsQL)TM questionnaire will be used to examine perceived health-related quality of life among participants. Grade 4 and Grade 5 at baseline, and immediately post-intervention (approx. 9-months after baseline). ]

次要结局

未报告次要终点

研究者

相似试验