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Clinical Trials/DRKS00019832
DRKS00019832
Completed
未知

Comparison of the effects of endurance and endurance-strength training on the endothelial dysfunction in women with abdominal obesity - ENDOFIT

The National Science Centre0 sites101 target enrollmentFebruary 26, 2020
ConditionsE66Obesity

Overview

Phase
未知
Intervention
Not specified
Conditions
E66
Sponsor
The National Science Centre
Enrollment
101
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 26, 2020
End Date
December 19, 2016
Last Updated
last year
Study Type
Interventional
Sex
Female

Investigators

Sponsor
The National Science Centre

Eligibility Criteria

Inclusion Criteria

  • Obesity (body mass index (BMI) \= 30 kg/m2\), waist circumference \> 80 cm; percentage of body fat assessed by bioimpedance \= 33% and stable body weight in the month prior to the trial (permissible deviation ± 1 kg).

Exclusion Criteria

  • Secondary form of obesity and/or secondary form of hypertension, type 2 diabetes mellitus, history of coronary artery disease, stroke (including transient ischaemic attack), congestive heart failure, clinically significant arrhythmias or conduction disorders, malignancy, history of use of any dietary supplements within 3 months before the study, poorly controlled hypertension (mean systolic blood pressure \> 140 mmHg and/or mean diastolic blood pressure \> 90 mmHg) during the month prior to the trial and/or necessity to modify antihypertensive treatment in the last 3 months, lipid disorders requiring the implementation of drug treatment in the last 3 months, abnormal liver, kidney, or thyroid gland function, clinically significant acute or chronic inflammatory process within the respiratory, digestive or genitourinary tract or in the oral cavity, pharynx or paranasal sinuses or connective tissue disease or arthritis, history of infection in the month, nicotine, alcohol or drug abuse, pregnancy or childbirth at enrolment or in the 3 months before enrolment, breast\-feeding in the 3 months prior to enrolment, any other condition that would make participation not in the best interests of the subject, or could prevent, limit or confound the efficacy of the study.

Outcomes

Primary Outcomes

Not specified

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