- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04711928
The Association Between Sedentary Behaviour and Cardiometabolic Health in Trained Athletes (HPAC)
March 14, 2022 updated by: Bert Op't Eijnde, Hasselt University
Do Trained Athletes Also Suffer From the Sedentary Behaviour Paradigm?: the Association Between Sedentary Behaviour and Cardiometabolic Health
Physical inactivity is one of the major contributing factors for the development of chronic diseases and highly correlated with increased all-cause mortality.
In the last decade an exponential growth in research concerned with the study of sedentary behaviour and the potential for detrimental effects on health have been published.
In this field increasing evidence suggests that prolonged periods of sedentary time, independent of the amount of physical activity, also increases the risk for the development of several chronic conditions and all-cause mortality.
Here, sedentary behaviour is defined as "any waking behaviour, characterized by a low energy expenditure (≤1.5 METs), while being in a sitting or reclining posture".
Interestingly, the advised moderate-to-vigorous bouts of exercise recommended by the various guidelines cannot compensate the negative impact on health risks arising from prolonged periods of sitting.
In other words, it seems that people compensate their total amount of physical activity after exercise training by decreasing their physical activity levels throughout the rest of the day.
Here, it appears that frequent, even low-intensity interruptions of periods of sitting are required for good cardiometabolic health.
Therefore, not only physical activity but also prolonged sitting should be targeted to optimize cardiometabolic health.
Nevertheless, a recent harmonized meta-syntheses indicated that the association between self-reported sitting with all-cause and cardiovascular disease mortality are only partially independent of physical activity, but were particularly evident in those who undertake insufficient physical activity (<150min/week).
However, it is unclear whether high amounts of objectively measured physical activity attenuates or even eliminates the detrimental effects of prolonged sitting.
In addition, it is still unclear whether high amounts of physical activity can preserve a healthy cardiometabolic risk profile, despite prolonged sitting.
Therefore, in this study we want to investigate the association between sedentary behaviour, physical activity and cardiometabolic health in highly physically active adults.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Limburg
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Diepenbeek, Limburg, Belgium, 3590
- Wouter Franssen
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 45 years (ADULT)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Active individuals with at least 4 training hours per week and between 18 and 45 years of age.
Description
Inclusion Criteria:
- Active individuals with at least 4 training hours per week
Exclusion Criteria:
- pregnancy
- Any known contradiction for physical activity
- Systolic blood pressure >160mmHg, diastolic blood pressure >100mmHg
- More than 20 alcohol consumptions per week
- Participants diagnosed with any known chronic disease
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Trained athletes
Active individuals with at least 4 training hours per week.
|
Athletes with a high physical activity and a low or high sedentary time
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Sedentary time (min/day)
Time Frame: day 1
|
Main outcome parameter of sedentary behaviour indication measured with ActivPAL3
|
day 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Moderate-to-vigorous physical activity time (min/day)
Time Frame: day 1
|
Physical activity parameter measured with ActivPAL3
|
day 1
|
Light physical activity time (min/day)
Time Frame: day 1
|
Physical activity parameter measured with ActivPAL3
|
day 1
|
Blood glucose concentration
Time Frame: day 1
|
Parameter of glucose homeostatis
|
day 1
|
Blood insulin concentration
Time Frame: day1
|
Parameter of glucose homeostatis
|
day1
|
Blood total cholesterol concentration
Time Frame: day 1
|
Parameter of lipid metabolism
|
day 1
|
Blood triglyceride concentration
Time Frame: day 1
|
Parameter of lipid metabolism
|
day 1
|
Blood high density lipoprotein concentration
Time Frame: day 1
|
Parameter of lipid metabolism
|
day 1
|
Blood low density lipoprotein concentration
Time Frame: day 1
|
Parameter of lipid metabolism
|
day 1
|
Fat mass (kg)
Time Frame: day 1
|
Parameter of body composition measured with DEXA-scan
|
day 1
|
Lean mass (kg)
Time Frame: day 1
|
Parameter of body composition measured with DEXA-scan
|
day 1
|
Systolic blood pressure
Time Frame: day 1
|
Parameter of cardiovascular health
|
day 1
|
Diastolic blood pressure
Time Frame: day 1
|
Parameter of cardiovascular health
|
day 1
|
Maximal oxygen uptake
Time Frame: day 1
|
Parameter of oxygen capacity measured with cardiopulmonary exercise testing
|
day 1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
January 10, 2021
Primary Completion (ACTUAL)
August 1, 2021
Study Completion (ACTUAL)
October 1, 2021
Study Registration Dates
First Submitted
January 13, 2021
First Submitted That Met QC Criteria
January 14, 2021
First Posted (ACTUAL)
January 15, 2021
Study Record Updates
Last Update Posted (ACTUAL)
March 15, 2022
Last Update Submitted That Met QC Criteria
March 14, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- CME2020/012
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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