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Long-term Follow-up of the Helsinki Businessmen Study (HBS)

2015年8月14日 更新者:Timo Strandberg、Helsinki University Central Hospital

Long-term Follow-up of the Helsinki Businessmen Study Cohort of Men Born in 1919-1934

The Helsinki Businessmen Study (HBS) is a clinico-epidemiological longitudinal study started in 1964. It also included a 5-year randomized, controlled multifactorial primary prevention trial of cardiovascular diseases between 1974-1980. The cohort is being actively followed-up through national registers since the 1980, and since 2000 with regular questionnaire surveys. Latest in 2015. Also clinical and laboratory studies have been performed in random subcohorts. Follow-up is ongoing with new hypothesis-generating research questions.

研究概览

地位

主动,不招人

详细说明

The Helsinki Businessmen Study (HBS) was originally a convenient cohort of male executives and businessmen (born 1919-1934, n=3490), who participated in health check-ups between 1964-1973, but since the beginning of 1970s it has developed into a clinico-epidemiological longitudinal study. Primary focus was on the prevention of cardiovascular diseases (CVD), but since 2000 focus has been shifting to geriatrics, and with its long follow-up (up to 50 years) HBS can be seen as a "life-course" study. Traditional CVD risk factors are available from the 1960s and in 1974 participants (available n=3310) were divided in groups according to their clinical status and CVD risk. Two high-risk groups (n=1222) and low-risk group (n=593) participated in a 5-year multifactorial primary prevention study in 1974-1980 (in-trial and post-trial results have been published in 1985 and 1991). The whole original cohort has been followed-up from national registers since 1985 and with regular questionnaire surveys since 2000. Random subcohorts have been studied clinically with laboratory and genetic examinations in 2003 and 2011. The latest questionnaire survey was performed in winter 2015 by which two thirds of the original cohort had died. Follow-up of the cohort is ongoing and new research questions formulated..

研究类型

观察性的

注册 (实际的)

3490

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

31年 至 46年 (成人)

接受健康志愿者

不

有资格学习的性别

男性

取样方法

非概率样本

研究人群

Originally a convenient cohort of male executives and businessmen (born 1919-1934, n=3490), who participated in health check-ups during 1964-1973, but since the beginning of 1970s it has developed into a clinic-epidemiological longitudinal study.

描述

Inclusion Criteria:

  • Participants of director studies at the Institute of Occupational Health in Helsinki, Finland, between 1964-1973

Exclusion Criteria:

  • Non-participants

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 观测模型:队列
  • 时间观点:预期

队列和干预

团体/队列
干预/治疗
Total, observational
Various cardiovascular risk groups described below
High-risk intervention
Healthy but at high risk in 1974
Multifactorial intervention with lifestyle changes and drugs as needed
High-risk control
Healthy but at high risk in 1974
Low-risk conrtol
Healthy and at low risk in 1974
Sick control
Medications or clinical disease in 1974
Refused
Refused or no response in 1974

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Total mortality: national registers
大体时间:change from baseline up to 612 months
change from baseline up to 612 months

次要结果测量

结果测量
大体时间
Health-related quality of life: questionnaire data
大体时间:change from baseline up to 612 months
change from baseline up to 612 months
Geriatric syndromes and disability: questionnaires, clinical examinations, registers
大体时间:change from baseline up to 612 months
change from baseline up to 612 months
Morbidity: self-report, national registers, hospital and autopsy records
大体时间:change from baseline up to 612 months
change from baseline up to 612 months
Medications: self-report, national registers
大体时间:change from baseline up to 612 months
change from baseline up to 612 months
Cause-specific mortality: national registers, autopsy records
大体时间:change from baseline up to 612 months
change from baseline up to 612 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Timo E Strandberg, MD、Helsinki University Central Hospital

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

1964年1月1日

初级完成 (预期的)

2040年12月1日

研究完成 (预期的)

2040年12月1日

研究注册日期

首次提交

2015年6月10日

首先提交符合 QC 标准的

2015年8月14日

首次发布 (估计)

2015年8月18日

研究记录更新

最后更新发布 (估计)

2015年8月18日

上次提交的符合 QC 标准的更新

2015年8月14日

最后验证

2015年8月1日

更多信息

与本研究相关的术语

其他相关的 MeSH 术语

其他研究编号

  • HBS Group

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