ChiCTR2200065425招募中Unknown
The effectiveness of patient navigator intervention in promoting the uptake of colorectal cancer screening for the average risks older adults in Hong Kong: a pilot study
适应症
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- CRC screening uptake
研究概览
简要总结
Phase 1
- Develop a training program for lay navigators in facilitating CRC screening uptake.
- Evaluate the effectiveness of the training program in improving the knowledge of CRC of the lay navigators by completing pretest and posttest related to the CRC knowledge.
- Evaluate the self-efficacy of lay navigators in providing PN intervention by completing pretest and posttest of self-efficacy scale.
- Evaluate the satisfaction of the program by the lay navigators after training. Phase 2
- Develop and implement an evidenced-based PN intervention to enhance the uptake of CRC screening for the average risk of older adults in Hong Kong.
- Evaluate the feasibility and acceptability of PN intervention by assessing the screening rate, recruitment rate, percentage of eligibility, consent rate, withdrawal rate during recruitment, attrition rate of the participants and satisfaction rate of the participants.
- Evaluate the preliminary effect of the PN intervention by the uptake rate of the CRC screening of the average risk older adults compared to control arm at baseline and 3 months after the intervention.
- Determine the preliminary effects of PN intervention on knowledge, perceived susceptibility, severity, benefits and barriers on CRC screening.
研究设计
- 研究类型
- Interventional
- 主要目的
- 随机平行对照
- 盲法
- The participants will be blinded for the allocation of intervention or control group.
入排标准
- 年龄范围
- 50 至 75(—)
- 性别
- Male
入选标准
- •Older adults aged 50-75 years;
- •Speak fluent Cantonese;
- •Education level up to secondary school to facilitate the delivery of the CRC information;
- •Have experience in CRC screening by using FOBT/FIT;
- •Willing to complete the training programme and act as lay navigator for the target participants.
- •Average-risk older adults who age 50 -75 will be recruited as participants in this study;
- •He/She should have no history of CRC, no chronic inflammation of the bowel, no first-degree relatives having CRC and have never screened for CRC.
排除标准
- •Have mental and cognitive problems;
- •Prior CRC cancer.
研究组 & 干预措施
干预组
Patient navigator intervention
对照组
wait-list control
结局指标
主要结局
CRC screening uptake
时间窗: 3 months after baselines
次要结局
未报告次要终点
研究者
研究点 (1)
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