Clinical Trial to Evaluate the Acceptance and Viability of Three Strategies in Birth Cohort Hepatitis C Screening
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 609
- 试验地点
- 2
- 主要终点
- Acceptance of the interventions
研究概览
简要总结
The main purpose of the study is to compare the acceptance and viability of three strategies aimed to screen hepatitis C virus (HCV) infection in a birth cohort by: a) invitation letter offering HCV screening with dried blood spot (DBS) testing at the primary care center, b) invitation letter offering both HCV and colorectal cancer (CCR) screening with faecal occult test (FOT) at the primary care center, and c) invitation letter offering self-collected screening at home for HCV and CCR.
详细描述
This is a prospective, randomized, study in which subjects of four different health areas will be invited to participate in three different screening strategies for HCV.
Hepatologists from a tertiary care hospital and general practitioners from four health areas will participate coordinating the study, to first select potential candidates for the study (subjects between 50 and 70 years old of the four areas) and secondly, randomize and include 150 subjects of each area into the three strategies (50 subjects each). The strategies include offering by letter screening at the local primary care center for HCV by using dried blood spot (DBS) testing, screening for HCV and colorectal cancer (CCR) using faecal occult test (FOT) at the primary care center, and self-testing at home-collection with DBS and FOT to be performed by the subject and sent by postal office. Subjects will receive an invitation and informative letter and will be ask to sign the informed consent to participate.
In all the planned strategies subjects will be asked to complete a questionnaire that includes demographic variables. After two months of sending the letters without response, researchers will contact subjects by phone to complete a survey to confirm they received the letter and asking for factors of non-participation.
The hypothesis of the study is that subjects in the risk of having HCV are willing to be screened for HCV infection if offered and that the acceptance will be improved if attached to CCR screening and even higher if the tests are offered to be self-screened.
For the present study, a 15% improvement in the participation (acceptance of the screening strategy) was hypothesized in the group of patients receiving the strategy 2 (and 3) compared to the strategy 1. Taking into account a power of 80%, alpha error of 5% and losses of 20% will require 200 patients per group.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Diagnostic
- 盲法
- None
入排标准
- 年龄范围
- 50 Years 至 70 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age 50-70 years
- •Subjects attending selected primary care centers
- •Willing to participate (informed consent signed)
排除标准
- 未提供
研究组 & 干预措施
Self-testing at home for screening HCV and CCR
Patients assigned to the strategy 3 will receive an invitation letter for self-testing at home for HCV screening with DBS, and CCR screening with FOT
干预措施: Screening HCV attached onto CCR screening by self-testing (Behavioral)
Screening HCV with DBS at primary care centers
Patients assigned to the strategy 1 will receive an invitation letter for HCV screening with DBS at the primary care center to be performed by the general practitioner
干预措施: Screening HCV at primary care center (Behavioral)
Screening HCV and CCR with FOT at primary care centers
Patients assigned to the strategy 2 will receive an invitation letter for HCV screening with DBS and CCR screening with FOT at the primary care center to be performed by the general practitioner
干预措施: Screening HCV attached onto CCR screening (Behavioral)
结局指标
主要结局
Acceptance of the interventions
时间窗: 12 months
overall screening rate (number of subjects participating after enrollment)
次要结局
- Effectiveness of each strategy: rate of HCV positivity(12 months)
- Feasibility of the intervention measuring quality of spotted cards(12 months)
- Subject characteristics associated with participation and feasibility of the different strategies(12 months)
研究者
Manuel Hernandez-Guerra, MD
Principal Investigator
University of La Laguna
