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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02526082
Other study ID # HBS Group
Secondary ID
Status Active, not recruiting
Phase N/A
First received June 10, 2015
Last updated August 14, 2015
Start date January 1964
Est. completion date December 2040

Study information

Verified date August 2015
Source Helsinki University Central Hospital
Contact n/a
Is FDA regulated No
Health authority Finland: Ethics Committee
Study type Observational

Clinical Trial Summary

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.


Description:

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..


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 3490
Est. completion date December 2040
Est. primary completion date December 2040
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 31 Years to 46 Years
Eligibility Inclusion Criteria:

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

Exclusion Criteria:

- Non-participants

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Intervention

Other:
Intervention
Multifactorial intervention with lifestyle changes and drugs as needed

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Helsinki University Central Hospital

References & Publications (3)

Miettinen TA, Huttunen JK, Naukkarinen V, Strandberg T, Mattila S, Kumlin T, Sarna S. Multifactorial primary prevention of cardiovascular diseases in middle-aged men. Risk factor changes, incidence, and mortality. JAMA. 1985 Oct 18;254(15):2097-102. — View Citation

Strandberg AY, Strandberg TE, Stenholm S, Salomaa VV, Pitkälä KH, Tilvis RS. Low midlife blood pressure, survival, comorbidity, and health-related quality of life in old age: the Helsinki Businessmen Study. J Hypertens. 2014 Sep;32(9):1797-804. doi: 10.10 — View Citation

Strandberg TE, Salomaa VV, Naukkarinen VA, Vanhanen HT, Sarna SJ, Miettinen TA. Long-term mortality after 5-year multifactorial primary prevention of cardiovascular diseases in middle-aged men. JAMA. 1991 Sep 4;266(9):1225-9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Total mortality: national registers change from baseline up to 612 months No
Secondary Health-related quality of life: questionnaire data change from baseline up to 612 months No
Secondary Geriatric syndromes and disability: questionnaires, clinical examinations, registers change from baseline up to 612 months No
Secondary Morbidity: self-report, national registers, hospital and autopsy records change from baseline up to 612 months No
Secondary Medications: self-report, national registers change from baseline up to 612 months No
Secondary Cause-specific mortality: national registers, autopsy records change from baseline up to 612 months No
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