- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05413434
Exercise Training and Respiratory Muscle Training in Individuals With Metabolic Syndrome(METS) (METS)
The Effects of Exercise Training and Respiratory Muscle Training on Physical Fitness, Pulmonary Functions and METS Parameters in Individuals With METS
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Metabolic syndrome (METS) is a systemic endocrinopathy characterized by the presence of risk factors such as abdominal obesity, glucose intolerance or diabetes mellitus, atherogenic dyslipidemia, hypertension, and a persistent proinflammatory profile. According to the International Diabetes Federation (IDF) definition of METS, almost 20-25% of the adult world population has METS, and people with METS are at risk of heart attack, stroke, type 2 diabetes (T2D), all-cause and cardiovascular death (approximately three times higher). In addition, modifiable risk factors such as physical inactivity, diet, and sedentary behavior have all been associated with increased prevalence of METS. Increasing incidence of METS, increase in morbidity and mortality necessitated the implementation of preventive strategies and the implementation of pharmacological and non-pharmacological treatments.
Studies in the literature have shown that vagal tone decreases and sympathetic tone increases in patients with METS. At the same time, impaired baroreflex sensitivity and decreased heart rate variability are observed in these patients. Changes in autonomic modulation cause the release of some bioactive molecules by affecting the endocrine and immune systems. In this case, increased sympathetic autonomic tone creates a cardiometabolic risk. In adults with METS, autonomic dysfunction appears to be more prominent in women than in men. Autonomic functions are impaired due to changes such as loss of lean body mass, increase in fat mass, increase in body mass, redistribution of fat from the periphery to the middle parts of the body, especially in postmenopausal women. As a result, increased blood pressure, impaired endothelial function, decreased glucose tolerance, and atherogenic changes in lipid and coagulation profiles can be observed. This increases the incidence of METS in postmenopausal women. Therefore, strategies to reduce the risk of metabolic syndrome have often been studied on women in the literature, and there is a need for studies involving men and new strategies.
Physical activity and exercise training are recommended as key prescriptions for the prevention and treatment of METS and low-grade chronic inflammation . Increase in physical exercise has been recommended for the prevention and primary treatment of cardiovascular disease (CVD) and METS because of the cardioprotective benefits associated with improved cardiorespiratory fitness (CRF). There are many studies showing that aerobic exercise provides significant improvements in waist circumference, fasting glucose, high-density lipoprotein cholesterol (HDL-C), TG, systolic and diastolic blood pressure (SBP-DBP), and cardiorespiratory fitness on METS parameters . However, although the beneficial effects of physical activity are known, only half of the population adheres to the 150 minutes of moderate-intensity physical activity per week recommendation. It has been shown that one of the main barriers to reaping health benefits and being more active is "lack of time". High-intensity interval training (HIIT) is a type of training that uses near-maximal intensities in short-term sessions. HIIT has been used to improve compliance because it requires less time to treat patients with cardiometabolic disease. Compared to continuous aerobic exercise, this type of training is an effective alternative to improve maximum oxygen consumption (VO2max), blood pressure, heart function, glucose and lipid metabolism, and markers of oxidative stress and inflammation . However, it has been seen that there are not enough studies on HIIT effectiveness on METS parameters in the literature. Therefore, researchers aimed to show the effects of HIIT training applied together with respiratory muscle training on METS parameters in patients with METS.
It has shown the beneficial effects of exercise training as well as inspiratory muscle training (IME) on autonomic function in patients with hypertension and heart disease . In a study, it was shown that 7-day inspiratory muscle training improved respiratory muscle functions and cardiac autonomic functions in postmenopausal women . As a result of this study, inspiratory muscle training has been proposed as a nonpharmacological strategy to improve autonomic modulation and reduce risk factors in individuals with METS, but further studies are required to confirm the long-term effects or effects of inspiratory muscle training in addition to classical exercise training protocols such as aerobic, resistance or combined training. are needed.
In a study conducted in healthy and middle-aged men and postmenopausal women in 2021, it was proven that high resistance inspiratory muscle strength training can improve blood pressure control and vascular endothelial function, and reduce the risk of cardiovascular disease and other clinical disorders. In this study, researchers presented the first evidence that inspiratory muscle strength training increases NO bioavailability, decreases systemic inflammation, and causes potentially beneficial changes in the plasma metabolome by increasing endothelial NO synthase activation and decreasing oxidative stress. In conclusion, it has been shown that inspiratory muscle strength training can be used as a promising lifestyle intervention to improve cardiovascular function and reduce the risk of other clinical disorders .
Since the long-term effects of respiratory muscle training in individuals with METS have not been examined in the literature; researchers planned this study to examine the effects of inspiratory muscle strength training added to aerobic exercise training (HIIT) on physical fitness, respiratory functions and METS parameters in individuals with METS.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Ankara, Turkey
- Hacettepe University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- METS will be defined according to the National Adult Cholesterol Education Program Adult Treatment Panel III. Patients with at least three or more of the following five characteristics will be included in the study:
- Waist circumference ≥102 cm for men or ≥88 cm for women;
- blood pressure above 130/85 mmHg;
- Fasting blood glucose (FG) ≥100 mg/dL;
- Blood TG ≥150 mg/dL; and
- HDL-C < 40 mg/dL for men and < 50 mg/dL for women.
- Not participating in any physical activity program (≤2 physical activity days per week ≤ 30 minutes per session).
- 18 -65 years
- to walk and cooperate
- to participate in the research
Exclusion Criteria:
- heart failure,
- pectoris,
- of myocardial infarction or stroke in less than one year,
- hypertension,
- cardiovascular or kidney disease,
- with peripheral vascular disease and any disease associated with exercise intolerance will be excluded.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: HIIT with a supervisor
These individuals will be given HIIT training on the treadmill, accompanied by a physiotherapist, 3 days a week for 8 weeks.
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high-intensity interval training will be performed on the treadmill.
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Experimental: Hiit and respiratory muscle training with a supervisor
HIIT program and respiratory muscle training will be applied to these individuals 3 days a week for 8 weeks.
|
high-intensity interval training will be performed on the treadmill.
Respiratory muscle strength exercise will be performed with the respiratory muscle strengthening device 'POWERbreathe Classic Light Resistance'.
|
|
No Intervention: control group
The importance of physical activity will be explained and appropriate physical activity recommendations will be made.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
VO2max
Time Frame: 8 weeks
|
Cardiorespiratory fitness will be performed using a cardiopulmonary exercise test (CPET) with a treadmill, using the measurement method (breath by breath) with each breath.
The modified Bruce protocol will be applied.VO2max will be recorded in ml/kg/min.
|
8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
functional capacity
Time Frame: 8 weeks
|
Functional capacity will be evaluated with a 1 minute sit-stand test.
The number of sit-ups will be noted.
|
8 weeks
|
|
flexibility
Time Frame: 8 weeks
|
flexibility will be evaluated with the functional reach test and sit and reach test.
Results will be recorded in cm.
|
8 weeks
|
|
systolic and diastolic blood pressure
Time Frame: 8 weeks
|
Systolic and diastolic blood pressure will be measured using a digital sphygmomanometer (BP710, Omron, Tokyo, Japan) and results will be recorded in millimeters of mercury (mmHg).
After the participants rest for 5 minutes in a sitting position, two measurements will be taken with an interval of 1 minute.
The average of the two measurements will be recorded in mmHg.
|
8 weeks
|
|
C-Reactive Protein (CRP)
Time Frame: 8 weeks
|
Fasting blood samples will be taken from the patients before and after the 8-week training, after 12 hours of fasting, at Hacettepe University Hospital, Department of Internal Medicine, General Internal Medicine.
It will be held in the morning, 48 hours after the end of the training.
CRP will be recorded in mg/dl.
|
8 weeks
|
|
Low Density Lipoprotein Cholesterol (LDL-C)
Time Frame: 8 weeks
|
Fasting blood samples will be taken from the patients before and after the 8-week training, after 12 hours of fasting, at Hacettepe University Hospital, Department of Internal Medicine, General Internal Medicine.
It will be held in the morning, 48 hours after the end of the training.
LDL-C will be recorded in mg/dl.
|
8 weeks
|
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High Density Lipoprotein Cholesterol (HDL-C)
Time Frame: 8 weeks
|
Fasting blood samples will be taken from the patients before and after the 8-week training, after 12 hours of fasting, at Hacettepe University Hospital, Department of Internal Medicine, General Internal Medicine.
It will be held in the morning, 48 hours after the end of the training.
HDL-C will be recorded in mg/dl.
|
8 weeks
|
|
Total Cholesterol
Time Frame: 8 weeks
|
Fasting blood samples will be taken from the patients before and after the 8-week training, after 12 hours of fasting, at Hacettepe University Hospital, Department of Internal Medicine, General Internal Medicine.
It will be held in the morning, 48 hours after the end of the training.
Total Cholesterol will be recorded in mg/dl.
|
8 weeks
|
|
Triglycerides(TC)
Time Frame: 8 weeks
|
Fasting blood samples will be taken from the patients before and after the 8-week training, after 12 hours of fasting, at Hacettepe University Hospital, Department of Internal Medicine, General Internal Medicine.
It will be held in the morning, 48 hours after the end of the training.
TC will be recorded in mg/dl.
|
8 weeks
|
|
Fasting blood glucose
Time Frame: 8 weeks
|
Fasting blood samples will be taken from the patients before and after the 8-week training, after 12 hours of fasting, at Hacettepe University Hospital, Department of Internal Medicine, General Internal Medicine.
It will be held in the morning, 48 hours after the end of the training.
Fasting blood glucose will be recorded in mg/dl.
|
8 weeks
|
|
Hemoglobin A1c(HbA1c)
Time Frame: 8 weeks
|
Fasting blood samples will be taken from the patients before and after the 8-week training, after 12 hours of fasting, at Hacettepe University Hospital, Department of Internal Medicine, General Internal Medicine.
It will be held in the morning, 48 hours after the end of the training.
HbA1c will be described in %.
|
8 weeks
|
|
spot urinalysis
Time Frame: 8 weeks
|
In the urine analysis, albumin, protein and creatinine values will be recorded as mg/dl.
|
8 weeks
|
|
height
Time Frame: 8 weeks
|
A non-flexible and sensitive up to 0.1 cm tape measure will be used to measure the height of the participants.Height will be recorded in centimeter(cm) .
|
8 weeks
|
|
body weight
Time Frame: 8 weeks
|
Body Composition Scale will be used for body composition measurement .
Body weight will be recorded in kilogram(kg).
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8 weeks
|
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Body mass index(BMI)
Time Frame: 8 weeks
|
Weight and height will be combined to report BMI in kg/m^2.
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8 weeks
|
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Body fat ratio
Time Frame: 8 weeks
|
Body fat ratio will be measured with 'MI Scala 2'.
It will be recorded in %.
|
8 weeks
|
|
Respiratory function
Time Frame: 8 weeks
|
Pulmonary function test parameters will be performed with a portable spirometer device in sitting position, taking into account the criteria of the American Thoracic Society and the European Respiratory Society.
Forced Vital Capacity (FVC %), Forced expiratory volume (FEV1%) ,Peak expiratory flow (PEF %), forced mid-expiratory flow (FEF25-75%) will be recorded.
|
8 weeks
|
|
respiratory muscle strength
Time Frame: 8 weeks
|
Respiratory muscle strength will be evaluated with a portable intraoral pressure gauge ('Micro Medical( MicroRPM), Rochester, UK).
Maximal inspiratory pressure and maximal expiratory pressure values will be recorded in centimeters of water(cmH2O).
|
8 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: oğuz uyaroglu, PHD, Hacettepe University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HacettepeKPR
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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