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【ChiCTR2500108726】The effects of theory-guided multimodal educational (TIME) programme on the faecal occult blood test uptake rates among adults at average-risk of colorectal cancer: A randomized controlled trial

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基本信息

登记号

ChiCTR2500108726

试验状态

尚未开始

药物名称

药物类型

规范名称

首次公示信息日的期

2025-09-04

临床申请受理号

靶点

适应症

Colorectal cancer

试验通俗题目

The effects of theory-guided multimodal educational (TIME) programme on the faecal occult blood test uptake rates among adults at average-risk of colorectal cancer: A randomized controlled trial

试验专业题目

The effects of theory-guided multimodal educational (TIME) programme on the faecal occult blood test uptake rates among adults at average-risk of colorectal cancer: A randomized controlled trial

申办单位信息

申请人联系人

申请人名称

联系人邮箱

联系人邮编

联系人通讯地址

临床试验信息

试验目的

i) To develop and implement the TIME programme among adults at average-risk of colorectal cancer (CRC). ii) To examine the effects of TIME programme on CRC uptake rates, perceived susceptibility to CRC, perceived severity of CRC, perceived barriers to CRC screening, perceived benefits of CRC screening, and self-efficacy. iii) To evaluate the participants’ satisfaction with the TIME programme.

试验分类

试验类型

随机平行对照

试验分期

其它

随机化

Block randomization will be used to assign the participants to the intervention group or wait-list control group in a 1:1 ratio with a block size of 8. An independent statistician will use a computer to generate a random assignment sequence of group identifiers. The sequence of group identifiers will be printed on identical cards and inserted into sequentially numbered, sealed opaque envelopes.

盲法

Due to the nature of the educational intervention and the use of a wait-list control group in this study, it is not possible for the study participants to be blinded to their group allocation.

试验项目经费来源

N/A

试验范围

目标入组人数

104

实际入组人数

第一例入组时间

2025-08-15

试验终止时间

2026-08-31

是否属于一致性

入选标准

1. aged between 50 and 75; 2. Hong Kong residents; 3. no symptoms of CRC; 4. no history of CRC, polyps or inflammatory bowel disease; 5. no family history of CRC; 6. able to access WhatsApp Messenger or WeChat; 7. able to read Chinese and communicate in Cantonese; 8. willing to be followed up by telephone.；

排除标准

Individuals who have undergone a faecal occult blood test (FOBT) in the past 2 years, a sigmoidoscopy in the past 5 years, or a colonoscopy in the past 10 years, as well as those who do not have a smartphone, are mentally incapable, have hearing or visual impairments, or are unable to provide informed consent will be excluded.；

研究者信息

研究负责人姓名

试验机构

The Chinese University of Hong Kong

研究负责人电话

研究负责人邮箱

研究负责人邮编

联系人通讯地址

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