跳至主要内容
临床试验/ChiCTR2200065425
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

Hong Kong Metropolitan University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年11月9日最近更新:
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

  1. Develop a training program for lay navigators in facilitating CRC screening uptake.
  2. 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.
  3. Evaluate the self-efficacy of lay navigators in providing PN intervention by completing pretest and posttest of self-efficacy scale.
  4. Evaluate the satisfaction of the program by the lay navigators after training. Phase 2
  5. 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.
  6. 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.
  7. 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.
  8. 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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