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临床试验/NCT04175015
NCT04175015撤回不适用

The SMARTY Trial: Evaluating the Effects of Colour of Candy on Perceptions of Taste. A Randomised Trial

National University of Ireland, Galway, Ireland1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2019年11月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
入组人数
150
试验地点
1
主要终点
Taste

研究概览

简要总结

The purpose of this trial is to determine if the colour of sweets (candy) effects taste.

详细描述

The purpose of this trial is to increase children's awareness of randomised controlled trials and gain insights into the best way to conduct a fair comparison. Everyday children are faced with health claims, some reliable and some not so reliable. The purpose of the SMARTY trial is to help children critically assess and develop a critical eye when it comes to information they encounter every day, in particular when it comes to their health. The SMARTY trial is a pragmatic, two group, parallel, randomised trial.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Participant)

盲法说明

Single - Participant

入排标准

年龄范围
4 Years 至 18 Years(Child, Adult)
性别
All
接受健康志愿者
是

入选标准

  • •parental/guardian consent obtained

排除标准

  • •unable or unwilling to ingest intervention.
  • •medical conditions which prohibit ingestion of intervention (ie allergy, intolerance etc)

研究组 & 干预措施

Experimental

Experimental

Participants will be randomised to eat an orange coloured smartie©

干预措施: Smartie© sweet/candy (Other)

Control Group

Active Comparator

Participants will be randomised to eat a pink coloured smartie ©

干预措施: Smartie© sweet/candy (Other)

结局指标

主要结局

Taste

时间窗: 15 minutes

Participants will be asked to indicate on visual scale how much they like the taste of the smartie© they ate using the 'single-item sleep quality scale (SQS)' . The SQS is a self-administered visual analogue scale on which respondents rate the overall quality of sleep over a 7-day recall period on a likert type scaling option from 0 to 10, according to the following five categories: 0 = terrible, 1-3 = poor, 4-6 = fair, 7-9 = good, and 10 = excellent .

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Prof. Declan Devane

Scientific Director, HRB-Trials Methodology Research Network

National University of Ireland, Galway, Ireland

研究点 (1)

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