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Fat-Associated Cardiovascular Organ Dysfunction

Fat-Associated Cardiovascular Organ Dysfunction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02805478
Acronym
FATCOR
Enrollment
618
Registered
2016-06-20
Start date
2009-09-05
Completion date
2017-04-30
Last updated
2020-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Overweight

Brief summary

This is an observational study of cardiovascular risk factors and arterial or cardiac function in subjects with overweight or obesity. Subjects must be between 30 and 65 years of age, have a body mass index \>27.0 kg/m2 and free from known heart disease and digestive or psychiatric disorders. Study aims include identifying sex-differences in traditional cardiovascular risk factors and structural and functional abnormalities in arteries and the heart in subjects with overweight or obesity, and how this is influenced by physical fitness.

Detailed description

FATCOR is an observational study of women and men with overweight or obesity. In particular prevalences of conventional cardiovascular risk factors and subclinical arterial or cardiac dysfunction are explored. The study aims at identifying sex differences in presence and clustering of cardiovascular risk factors and presence of subclinical cardiovascular organ damage. The influence of physical fitness on these factors will also be assessed. All participants undergo extensive cardiovascular risk factor assessment including oral glucose tolerance test and ambulatory blood pressure recording. Subclinical cardiovascular dysfunction is assessed by carotid and femoral vascular ultrasound, echocardiography and carotid-femoral pulse wave velocity using applanation tonometry. Physical fitness is assessed from peak oxygen uptake during maximal exercise testing on a treadmill.

Interventions

OTHERThere is no intervention

This is a prospective observational cohort study without any intervention

Sponsors

Haukeland University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* body mass index \> 27.0 kg/m2

Exclusion criteria

* known heart disease * digestive disorder * psychiatric disorder * unfamiliar with Norwegian language

Design outcomes

Primary

MeasureTime frameDescription
Abnormal left ventricular geometryAt study baselineEchocardiography
Dilated left atriumAt study baselineEchocardiography

Secondary

MeasureTime frameDescription
Relation of physical fitness to prevalence of cardiovascular risk factorsAt study baselineCardiopulmonary exercise
Relation of sex to prevalence of hypertensionAt study baselineAmbulatory blood pressure recording
Relation of sex to abnormal left ventricular geometryAt study baselineEchocardiography
Relation of sex to arterial stiffnessAt study baselineApplanation tonometry

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026