跳至主要内容
临床试验/NCT06972160
NCT06972160招募中不适用

Interventions to Increase Adherence to Colorectal Cancer Screening in Barcelos/Esposende: a Randomized Clinical Trial

Local Health Unit Barcelos/Esposende, Public Health Unit1 个研究点 分布在 1 个国家目标入组 1,038 人开始时间: 2025年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
1,038
试验地点
1
主要终点
Adherence to colon and rectal screening [Time Frame: 6 weeks]

研究概览

简要总结

An experimental study through a randomized clinical trial, without blinding (for participants and the research team), with a control group (not subject to intervention) and an intervention group (subject to two text messages, an automated non-human call or a call made by the administrative assistant, and a phone call made by a physician).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Screening
盲法
None

入排标准

年龄范围
49 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Participants must be registered in the ULS of
  • •Barcelos/Esposende and meet the following criteria:
  • •Age between 50 and 74 years.
  • •No symptoms such as weight loss in the last 6 months or gastrointestinal symptoms.
  • •No prior diagnosis of CRC.
  • •No diagnosis of inflammatory bowel disease (ulcerative colitis or Crohn's disease).
  • •No family history of CRC in first- and second-degree relatives diagnosed before age
  • •No prior fecal occult blood test (FOBT) in the 11 months before receiving the collection kit or no prior sigmoidoscopy or colonoscopy in the last 24 months.

排除标准

  • •Participants who did not receive the screening kit at home.
  • •Participants without a phone number.
  • •Participants who do not answer the phone or refuse to participate in the study.
  • •Participants unable to consent or perform the screening due to physical, mental, or other conditions that seriously impair comprehension.

研究组 & 干预措施

Interventional Group

Experimental

The interventional group will be subjected to interventions to increase the adherence to screening, including text messages via phone as well as phone calls.

干预措施: Arm1: intervention 1 (SMS+call) (Other)

Control group

Placebo Comparator

The control group will not be subjected to any interventions to increase the adherence to screening.

干预措施: Control group (Other)

结局指标

主要结局

Adherence to colon and rectal screening [Time Frame: 6 weeks]

时间窗: From April 2025 to June 2025 (6 weeks)

Increase in adherence to colon and rectal screening Proportion/cumulative proportion of patients who performed colon and rectal cancer screening among those who were invited to undergo it, after step 1 (SMS1), step 2 (SMS2), step 3 (administrative call) and step 4 (medical doctor call)

次要结局

未报告次要终点

研究者

发起方
Local Health Unit Barcelos/Esposende, Public Health Unit
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

David Nascimento Moreira

Public Health Medical Doctor, Local Health Authority

Instituto de Saude Publica da Universidade do Porto

研究点 (1)

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