- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03986879
Relationship of the Physical Activity Practice and Its Different Domains With Cardiac Autonomic Modulation
November 13, 2023 updated by: Bruna Thamyres Ciccotti Saraiva
Relationship of the Intensity of Physical Activity Practice and Its Different Domains With Cardiac Autonomic Modulation in Adult Individuals
Overall objective: To analyze the relationship of the physical activity practice measured directly with the autonomic cardiac modulation in adults.
Specific objectives: i) to verify through the Baecke questionnaire whether the different domains of physical activity (work, leisure and occupational activities) are related in the same way to the autonomic cardiac modulation; ii) Analyze whether high blood pressure and resting heart rate values are related to poor cardiac autonomic modulation regardless of nutritional status.
Study Overview
Status
Active, not recruiting
Conditions
Detailed Description
Cardiovascular disease is a major public health problem and has contributed to a high mortality rate in the adult population.
One of the precursors of these diseases is low cardiac autonomic modulation.
Thus, factors that may be related to greater cardiac autonomic modulation should be investigated with the aim of preventing cardiovascular diseases.
One of these factors that may contribute to increases in cardiac autonomic modulation is the practice of physical activity.
However, the studies investigating this relationship have been controversial, generally evaluating the practice of physical activity in a subjective way, and there is no clarity as to whether the different domains of physical activity would be related differently to cardiac autonomic modulation.
Overall objective: To analyze the relationship of the physical activity practice measured directly with the autonomic cardiac modulation in adults.
Specific objectives: i) to verify through the Baecke questionnaire whether the different domains of physical activity (work, leisure and occupational activities) are related in the same way to the autonomic cardiac modulation; ii) Analyze whether high blood pressure and resting heart rate values are related to poor cardiac autonomic modulation regardless of nutritional status.
Implications: The results of this study will contribute to clarify the relationship between physical activity practice and cardiac autonomic modulation considering a large sample of subjects (n = 252), as well as whether the different domains of physical activity are related to autonomic modulation cardiac.
These results may help in the elaboration of health promotion strategies.
Study Type
Observational
Enrollment (Estimated)
252
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
-
-
Sao Paulo
-
Presidente Prudente, Sao Paulo, Brazil, 19060-900
- Diego Giulliano Destro Christofaro
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
The sample will be composed of adults aged 18 years or older from the city of Santo Anastácio-SP located in the southeastern region of Brazil.
Description
Inclusion Criteria:
- 18 years or older
- be resident of the city of Anastácio-SP (Brazil)
- sign the informed consent form
Exclusion Criteria:
- use less than 5 valid accelerometer days
- present an error in heart rate variability greater than 5%
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
- Observational Models: Other
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cardiac autonomic modulation
Time Frame: through study completion, an average of 1 year
|
The heart rate variability will be collected by means of the POLAR V800.
|
through study completion, an average of 1 year
|
Physical activity level - objective measure
Time Frame: through study completion, an average of 1 year
|
Will be collected 7 days of accelerometry by ActiGraph's triaxial accelerometer wGT3X-BT giving the measure in counts per minute.
|
through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Self-reported physical activity level questionnaire
Time Frame: through study completion, an average of 1 year
|
Physical activity in different domains will be evaluated by the Baecke et al. (1982).
This instrument evaluates the practice of physical activity through 16 questions in the last twelve months, considering the physical effort at work, the practice of sports activities or systematized exercises in leisure and leisure activities.
At the end, this instrument offers a dimensionless score for each of the domains and the sum of the score of the three domains also determines the total amount of physical activity practiced by each of the evaluated individuals.
|
through study completion, an average of 1 year
|
Systolic Blood pressure
Time Frame: through study completion, an average of 1 year
|
The systolic blood pressure will be measured by means of the omron digital oscillometric device.
|
through study completion, an average of 1 year
|
Diastolic Blood pressure
Time Frame: through study completion, an average of 1 year
|
The diastolic blood pressure will be measured by means of the omron digital oscillometric device.
|
through study completion, an average of 1 year
|
Self-reported practice of physical activity in childhood and adolescence
Time Frame: through study completion, an average of 1 year
|
To evaluate the practice of physical activity in childhood (age 7 to 10 years) and adolescence (11-17 years) two questions will be asked: if they practiced some kind of sport in these phases of life with supervision of a teacher, with two alternatives of answer: yes or no.
|
through study completion, an average of 1 year
|
Resting Heart Rate
Time Frame: through study completion, an average of 1 year
|
The resting heart rate will be measured by means of the omron digital oscillometric device.
|
through study completion, an average of 1 year
|
Body Mass
Time Frame: through study completion, an average of 1 year
|
Individuals will be evaluated barefoot wearing light clothing.
Body mass will be measured by means of a digital scale (Plenna, Brazil)
|
through study completion, an average of 1 year
|
Height
Time Frame: through study completion, an average of 1 year
|
Individuals will be evaluated barefoot wearing light clothing.
The height will be evaluated by a fixed stadiometer on the wall.
|
through study completion, an average of 1 year
|
Body Mass Index
Time Frame: through study completion, an average of 1 year
|
The body mass index (BMI) will be calculated by dividing the body mass by the square of the height.
Individuals classified up to 24.99 kg/m² will be considered as normal weight, those classified as having a BMI varying from 25.00 kg/m² up to 29.99 kg/m² will be classified as overweight and those with BMI ≥ 30 kg/m² as obese.
|
through study completion, an average of 1 year
|
Waist Circumference
Time Frame: through study completion, an average of 1 year
|
The waist circumference will be evaluated by an inextensible tape (Sanny, Brazil) and will consider the smallest circumference between the last rib and the iliac crest.
Abdominal obesity will be considered in men with waist circumference ≥102 cm and women at 88 cm, following the recommendations of the World Health Organization (WHO, 1997).
|
through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Diego GD Christofaro, PhD, Universidade Estadual Paulista - UNESP
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Tebar WR, Ritti-Dias RM, Mota J, Saraiva BTC, Damato TM, Delfino LD, Farah BQ, Vanderlei LCM, Christofaro DGD. Relationship of Cardiac Autonomic Modulation with Cardiovascular Parameters in Adults, According to Body Mass Index and Physical Activity. J Cardiovasc Transl Res. 2021 Oct;14(5):975-983. doi: 10.1007/s12265-021-10101-3. Epub 2021 Jan 22.
- Tebar WR, Ritti-Dias RM, Saraiva BTC, Gil FCS, Delfino LD, Damato TMM, Aguilar BAS, Silva SCB, Mota J, Vanderlei LCM, Christofaro DGD. The relationship between physical activity intensity and domains with cardiac autonomic modulation in adults: An observational protocol study. Medicine (Baltimore). 2019 Oct;98(41):e17400. doi: 10.1097/MD.0000000000017400.
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)
November 10, 2018
Primary Completion (Actual)
November 10, 2023
Study Completion (Estimated)
December 10, 2023
Study Registration Dates
First Submitted
May 30, 2019
First Submitted That Met QC Criteria
June 11, 2019
First Posted (Actual)
June 14, 2019
Study Record Updates
Last Update Posted (Estimated)
November 14, 2023
Last Update Submitted That Met QC Criteria
November 13, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 72191717.9.0000.5402
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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