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The Effect of 12-week Circuit Training on Insulin Sensitivity and Endothelial Function in Women With Insulin Resistance

Primary Purpose

Insulin Resistance

Status
Active
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Circuit training (combination of strength and endurance exercises)
Sponsored by
Poznan University of Physical Education
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Insulin Resistance focused on measuring circuit training, combined training, endothelial function, insulin sensitivity, lipid metabolism, inflammation, myokines, plantar stifness, back pain

Eligibility Criteria

25 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • women,
  • age: 25-45years,
  • menstruating,
  • BMI 18,5-29,9 kg/m2,
  • insulin resistance based on HOMA -IR (cut-off point 2.5),
  • not contraindicated to physical activity.

Exclusion Criteria:

  • type 1 and 2 diabetes,
  • poorly controlled hypertension (mean SBP >140mmHg and/or mean DBP >90mmHg) over the last month and/or need to modify the pharmacological treatment,
  • obesity: BMI > 30 kg/m2,
  • lipid disorders requiring implementation of pharmacological treatment in the last 3 months before or during observation,
  • a positive history of ischemic heart disease, carotid atherosclerosis and / or lower limb atherosclerosis,
  • clinically significant arrhythmias or conduction disorders,
  • chronickidney disease,
  • clinically significant liver dysfunction,
  • acute or chronic, clinically manifest inflammatory process,
  • an acute infection in the last month,
  • cancer,
  • taking dietary supplements within a month before inclusion and during observation,
  • taking medication that could interfere with the results of the tests,
  • other conditions that may pose any risk to the patient during the observation.

Sites / Locations

  • Poznan University of Physical Education

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Control

Arm Description

40 women with insulin resistance aged 25-45, BMI 18,5-29,9 will perform, for a period of 3 months, 3 times a week, strength training, interspersed with bouts of endurance exercise carried out on circuit machines integrated with the Milon computer software.

40 women with insulin resistance aged 25-45, BMI 18,5-29,9 will be asked to maintain their current level of physical activity and their diet for a period of 3 months.

Outcomes

Primary Outcome Measures

Homeostasis model assessment of insulin resistance (HOMA-IR)
Homeostasis model assessment of insulin resistance (HOMA-IR)
HbA1C [mmol/mol]
ELISA
HbA1C [mmol/mol]
ELISA
Insuline [mU/ml]
Radioimmunoassay
Insuline [mU/ml]
Radioimmunoassay
Systolic and diastolic blood pressure [mmHg]
Systolic and diastolic blood pressure [mmHg]
Pulse wave velocity (PWV) [m/s]
PWV will be performed using the SphygmoCor Px (Atcor Medical Blood Pressure Analysis System, Sydney, Australia.
Pulse wave velocity (PWV) [m/s]
PWV will be performed using the SphygmoCor Px (Atcor Medical Blood Pressure Analysis System, Sydney, Australia.
Glucose, Total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C) and triglycerides (TG) [mmol/l]
Dimension Flex Reagent Cartridge
Glucose, Total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C) and triglycerides (TG) [mmol/l]
Dimension Flex Reagent Cartridge
Irisin, Visfatin, Retinol-binding protein 4 (RBP-4) [pg/ml]
ELISA
Irisin, Visfatin, Retinol-binding protein 4 (RBP-4) [pg/ml]
ELISA
Apelin [ng/ml]
ELISA
Apelin [ng/ml]
ELISA
C Reactive Protein (hsCRP) [mg/l]
ELISA
C Reactive Protein (hsCRP) [mg/l]
ELISA
Interleukin-6 (IL-6), Interleukin-10 (IL-10) [pg/ml]
ELISA
Interleukin-6 (IL-6), Interleukin-10 (IL-10) [pg/ml]
ELISA
Endothelial nitric oxide synthase (eNOS) [ng/ml]
ELISA
Endothelial nitric oxide synthase (eNOS) [ng/ml]
ELISA
Muscle strength [kg]
Test 1RM will be performed for following groups of muscles: abdominal muscles; back of the thigh (biceps femoris muscle and muscles adjacent to it); latissimus dorsi muscle, shoulder girdle muscles and upper chest; erector spinae and other muscles of a back; gluteal muscles, hip adductor and abductor muscles.
Muscle strength [kg]
Test 1RM will be performed for following groups of muscles: abdominal muscles; back of the thigh (biceps femoris muscle and muscles adjacent to it); latissimus dorsi muscle, shoulder girdle muscles and upper chest; erector spinae and other muscles of a back; gluteal muscles, hip adductor and abductor muscles.

Secondary Outcome Measures

Plantar stiffness [N/m]
Biomechanical properties will be assessed with myotonometer device.
Plantar stiffness [N/m]
Biomechanical properties will be assessed with myotonometer device.
State of tension of erector spinae muscles [Hz]
Natural oscillation frequency [Hz], characterizing Tone or Tension will be assessed with myotonometer device.
State of tension of erector spinae muscles [Hz]
Natural oscillation frequency [Hz], characterizing Tone or Tension will be assessed with myotonometer device.
Low back pain intensity: questionnaire
Visual analogue scale (VAS) pain intensity questionare (reporting a score on a 10-point scale, the minimum (0) means no pain and the maximum (10) means a worst pain imaginable
Low back pain intensity: questionnaire
Visual analogue scale (VAS) pain intensity questionare (reporting a score on a 10-point scale, the minimum (0) means no pain and the maximum (10) means a worst pain imaginable
Disability caused by pain in the spine
Oswestry questionnaire. When completing the questionnaire, the subject answers questions concerning: pain intensity, independence, lifting objects, walking, sitting, standing, sleeping, social life, sexual activity and traveling. The answers to the questions help to classify how limited the functioning of the patient is while performing certain activities. Responses are graded from 0 to 5. The overall score is given on a 0-50 point scale, where the higher the score, the greater the disability.
Disability caused by pain in the spine
Oswestry questionnaire. When completing the questionnaire, the subject answers questions concerning: pain intensity, independence, lifting objects, walking, sitting, standing, sleeping, social life, sexual activity and traveling. The answers to the questions help to classify how limited the functioning of the patient is while performing certain activities. Responses are graded from 0 to 5. The overall score is given on a 0-50 point scale, where the higher the score, the greater the disability.

Full Information

First Posted
August 23, 2020
Last Updated
April 11, 2023
Sponsor
Poznan University of Physical Education
Collaborators
Poznan University of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT04528693
Brief Title
The Effect of 12-week Circuit Training on Insulin Sensitivity and Endothelial Function in Women With Insulin Resistance
Official Title
The Effect of 12-week Circuit Training (Combination of Strength and Endurance Exercises) on Insulin Sensitivity and Vascular Endothelial Function in Women With Insulin Resistance
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
August 17, 2020 (Actual)
Primary Completion Date
December 31, 2022 (Actual)
Study Completion Date
June 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Poznan University of Physical Education
Collaborators
Poznan University of Medical Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
During the last 10 years many studies concerning the impact of physical training on whole-body insulin sensitivity have been published, but there is a lack of an extended investigation on the potential clinical benefits of novel circuit training-based on strength and endurance exercises-relating to the optimization of insulin sensitivity and vascular endothelial function. It is of interest to precisely determine the physiological and biochemical effects of circuit training. An important aspect of the planned research will be the analysis of the effects of physical training on the released during muscle contraction myokines capable of modulating various metabolic processes. We hypothesized that in studied participants 12 weeks of the novel form of training would result in improving insulin sensitivity and vascular endothelial function mainly via myokines released by contracting skeletal muscles. The following questions will be asked: (1) whether the 12-week circuit training (combined strength and endurance exercises) performed by women with insulin resistance, improves insulin sensitivity, carbohydrate and lipid metabolism and promotes the efficiency of endothelial defense mechanisms? (2) whether the 12-week circuit training (combined of strength and endurance exercises) changes the concentrations of transcription factors regulating lipid and carbohydrate metabolism or the synthesis and/or secretion of myokines and adipokines in women with insulin resistance? (3) whether the 12-week strength training, interspersed with bouts of endurance exercise has a positive effect on cytokine profile? (4) whether there is a relationship between changes in body composition, HOMA-IR, and the level of myokines caused by physical training? (5) whether the 12-week circuit training reduces low back pain symptoms, plantar stifness and improve functioning of the patient in everyday life? A group of 80 women, aged 25 to 45 years, with diagnosed insulin resistance will participate in the planned study. Participants will be enrolled in the research program based on medical qualification. Before the intervention all women will have venous blood collected to determine fasting glucose, hemoglobin glycosylated (HbA1C) and insulin levels and insulin resistance by the homeostasis model assessment of insulin resistance (HOMA-IR) will be calculated. The inclusion criteria will be as follows: (1) women, age: 25-45 years, menstruating, (2) BMI 18,5-29,9 kg/m2, (3) insulin resistance based on HOMA-IR (cut-off point 2.5), (4) HbA1C ≤ 6.5%, (5) not contraindicated to physical activity. Participants meeting the inclusion criteria will be randomly divided into two groups. The first group of women will undergo circuit training, consisting of exercises performed on 7 machines arranged in a circuit. Thanks to the use of adequate software the machines will automatically adjust their parameters, such as seat height or resistance to the exercising person, and the training progress will be individually monitored. The planned training will last for 3 months, during which the patients will exercise 3 times a week for 30 minutes (2 circuits will be done during each session). The planned duration of the training session will be controlled (one minute for strength exercises, four minutes for endurance exercises and a 30-second break between each exercise). In the training group, one-repetition maximum exercise test (1RM) will be performed to determine the appropriate training load and later after the program to verify the increase in muscle strength. The range of maximum heart rate (HRmax) will also be determined in all exercising women. The second group of women, who will be asked to maintain their current level of physical activity and their diet for a period of 3 months will serve as a control group. Before and after the training program in all participants of the study pulse wave velocity, anthropometric parameters and body composition will be assessed. Concurrently venous blood will be taken to determine biochemical indicators related to carbohydrate and lipid metabolism, insulin resistance, vascular endothelium function, inflammation and adipocytokines and myokines. In both groups of women, the questioners concerning dietary intake and the level of daily physical activity will be administered. Results will be subjected to analysis involving descriptive, and advanced statistic method among them analysis of correlations, regression, variance and cluster analysis. All calculations and statistics will be performed using TIBCO Statistica 13.3 software (TIBCO).
Detailed Description
The training program will be performed on 7 machinesin a circuit. The devices will be controlled by a pre-programmed chip card, so that they will automatically adjust their parameters, such as seat height or resistance to the patient, and it will be possible to monitor the training progress of exercising women and their presence during training. Only two people will be allowed in the room during the training. The planned duration of the exercises will be controlled (one minute for strength exercises, four minutes for endurance exercisesand a 30-second break between each exercise) and for each trainee the load will be dosed using the electronic resistance motor system. Exercises in the training program are planned in such a way that the different muscle groups of women exercising are loaded alternately, which will ensure comprehensive training of the whole body. The range of movement, exercise duration and breaks will be controlled automatically by the system and the software of the devices and will not require additional training attention. In the training group, one-repetition maximum exercise test (1RM) will be performed to determine the appropriate training load and later after the program to verify the increase in muscle strength. The HR max range will be determined for exercising women by the indirect method using the formula: training HR = 220 -subject age. The characteristics of exercises in the circuit: The training circuit starts with an exercise on a cycloergometer -"bike", which lasts 4 minutes. The second exercise -"abdominal crunch", shapes the strength of the abdominal muscles and together with exercise number six, it not only improves muscle strength parameters, but also shapes balance and maintains the correct position of the body. The third exercisein a circuit-"leg curl", shapes the muscular strength of the back of the thigh (biceps femoris muscleand muscles adjacent to it). The fourth exercise -"lat pulldown", trains the strength of the latissimus dorsi muscle, shoulder girdle muscles and upper chest. In addition to improving the strength and function of the muscles mentioned above, the exercise also perfectly stimulates the auxiliary respiratory muscles. Fifth exercise -"crosswalker".This exercise trainsmost of the body's muscles, itlasts 4 minutes and, like training on a cycloergometer, primarily shapes thephysical capacity. The sixth exercise -"back extension"trains the strength of the abdominal muscles, erector spinae and other muscles of a back. The seventh exercise -"legabductor", the last in the series, is an exercise that shapes the gluteal muscles, as well as hip adductor and abductor muscles. This exercise fulfills the function of shaping strength and securing the hip joint, by training the muscle parts less frequently used in everyday life, the more difficult to be kept fit as the years go by and the level of physical activity decreases.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Insulin Resistance
Keywords
circuit training, combined training, endothelial function, insulin sensitivity, lipid metabolism, inflammation, myokines, plantar stifness, back pain

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study is designed as a prospective randomized clinical trial where subjects are randomally allocated to intervention group (study) or non-intervention group (control).
Masking
Care Provider
Masking Description
The qualifying physician does not know which of the examined persons will be allocated in the intervention or in the control group.
Allocation
Randomized
Enrollment
49 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
40 women with insulin resistance aged 25-45, BMI 18,5-29,9 will perform, for a period of 3 months, 3 times a week, strength training, interspersed with bouts of endurance exercise carried out on circuit machines integrated with the Milon computer software.
Arm Title
Control
Arm Type
No Intervention
Arm Description
40 women with insulin resistance aged 25-45, BMI 18,5-29,9 will be asked to maintain their current level of physical activity and their diet for a period of 3 months.
Intervention Type
Behavioral
Intervention Name(s)
Circuit training (combination of strength and endurance exercises)
Other Intervention Name(s)
Circuit training on machines integrated with the Milon computer software
Intervention Description
The intervention will last 3 months, exercises will take place 3 times a week and will consist of strength exercises, interspersed with bouts of endurance exercise carried out on circuit machines integrated with the Milon computer software for a total of 30 minutes per session.
Primary Outcome Measure Information:
Title
Homeostasis model assessment of insulin resistance (HOMA-IR)
Time Frame
pre-intervention
Title
Homeostasis model assessment of insulin resistance (HOMA-IR)
Time Frame
48 hours after the intervention
Title
HbA1C [mmol/mol]
Description
ELISA
Time Frame
pre-intervention
Title
HbA1C [mmol/mol]
Description
ELISA
Time Frame
48 hours after the intervention
Title
Insuline [mU/ml]
Description
Radioimmunoassay
Time Frame
pre-intervention
Title
Insuline [mU/ml]
Description
Radioimmunoassay
Time Frame
48 hours after the intervention
Title
Systolic and diastolic blood pressure [mmHg]
Time Frame
pre-intervention
Title
Systolic and diastolic blood pressure [mmHg]
Time Frame
48 hours after the intervention
Title
Pulse wave velocity (PWV) [m/s]
Description
PWV will be performed using the SphygmoCor Px (Atcor Medical Blood Pressure Analysis System, Sydney, Australia.
Time Frame
pre-intervention
Title
Pulse wave velocity (PWV) [m/s]
Description
PWV will be performed using the SphygmoCor Px (Atcor Medical Blood Pressure Analysis System, Sydney, Australia.
Time Frame
48 hours after the intervention
Title
Glucose, Total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C) and triglycerides (TG) [mmol/l]
Description
Dimension Flex Reagent Cartridge
Time Frame
pre-intervention
Title
Glucose, Total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C) and triglycerides (TG) [mmol/l]
Description
Dimension Flex Reagent Cartridge
Time Frame
48 hours after the intervention
Title
Irisin, Visfatin, Retinol-binding protein 4 (RBP-4) [pg/ml]
Description
ELISA
Time Frame
pre-intervention
Title
Irisin, Visfatin, Retinol-binding protein 4 (RBP-4) [pg/ml]
Description
ELISA
Time Frame
48 hours after the intervention
Title
Apelin [ng/ml]
Description
ELISA
Time Frame
pre-intervention
Title
Apelin [ng/ml]
Description
ELISA
Time Frame
48 hours after the intervention
Title
C Reactive Protein (hsCRP) [mg/l]
Description
ELISA
Time Frame
pre-intervention
Title
C Reactive Protein (hsCRP) [mg/l]
Description
ELISA
Time Frame
48 hours after the intervention
Title
Interleukin-6 (IL-6), Interleukin-10 (IL-10) [pg/ml]
Description
ELISA
Time Frame
pre-intervention
Title
Interleukin-6 (IL-6), Interleukin-10 (IL-10) [pg/ml]
Description
ELISA
Time Frame
48 hours after the intervention
Title
Endothelial nitric oxide synthase (eNOS) [ng/ml]
Description
ELISA
Time Frame
pre-intervention
Title
Endothelial nitric oxide synthase (eNOS) [ng/ml]
Description
ELISA
Time Frame
48 hours after the intervention
Title
Muscle strength [kg]
Description
Test 1RM will be performed for following groups of muscles: abdominal muscles; back of the thigh (biceps femoris muscle and muscles adjacent to it); latissimus dorsi muscle, shoulder girdle muscles and upper chest; erector spinae and other muscles of a back; gluteal muscles, hip adductor and abductor muscles.
Time Frame
pre-intervention
Title
Muscle strength [kg]
Description
Test 1RM will be performed for following groups of muscles: abdominal muscles; back of the thigh (biceps femoris muscle and muscles adjacent to it); latissimus dorsi muscle, shoulder girdle muscles and upper chest; erector spinae and other muscles of a back; gluteal muscles, hip adductor and abductor muscles.
Time Frame
48 hours after the intervention
Secondary Outcome Measure Information:
Title
Plantar stiffness [N/m]
Description
Biomechanical properties will be assessed with myotonometer device.
Time Frame
pre-intervention
Title
Plantar stiffness [N/m]
Description
Biomechanical properties will be assessed with myotonometer device.
Time Frame
48 hours after the intervention
Title
State of tension of erector spinae muscles [Hz]
Description
Natural oscillation frequency [Hz], characterizing Tone or Tension will be assessed with myotonometer device.
Time Frame
pre-intervention
Title
State of tension of erector spinae muscles [Hz]
Description
Natural oscillation frequency [Hz], characterizing Tone or Tension will be assessed with myotonometer device.
Time Frame
48 hours after the intervention
Title
Low back pain intensity: questionnaire
Description
Visual analogue scale (VAS) pain intensity questionare (reporting a score on a 10-point scale, the minimum (0) means no pain and the maximum (10) means a worst pain imaginable
Time Frame
pre-intervention
Title
Low back pain intensity: questionnaire
Description
Visual analogue scale (VAS) pain intensity questionare (reporting a score on a 10-point scale, the minimum (0) means no pain and the maximum (10) means a worst pain imaginable
Time Frame
48 hours after the intervention
Title
Disability caused by pain in the spine
Description
Oswestry questionnaire. When completing the questionnaire, the subject answers questions concerning: pain intensity, independence, lifting objects, walking, sitting, standing, sleeping, social life, sexual activity and traveling. The answers to the questions help to classify how limited the functioning of the patient is while performing certain activities. Responses are graded from 0 to 5. The overall score is given on a 0-50 point scale, where the higher the score, the greater the disability.
Time Frame
pre-intervention
Title
Disability caused by pain in the spine
Description
Oswestry questionnaire. When completing the questionnaire, the subject answers questions concerning: pain intensity, independence, lifting objects, walking, sitting, standing, sleeping, social life, sexual activity and traveling. The answers to the questions help to classify how limited the functioning of the patient is while performing certain activities. Responses are graded from 0 to 5. The overall score is given on a 0-50 point scale, where the higher the score, the greater the disability.
Time Frame
48 hours after the intervention

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: women, age: 25-45years, menstruating, BMI 18,5-29,9 kg/m2, insulin resistance based on HOMA -IR (cut-off point 2.5), not contraindicated to physical activity. Exclusion Criteria: type 1 and 2 diabetes, poorly controlled hypertension (mean SBP >140mmHg and/or mean DBP >90mmHg) over the last month and/or need to modify the pharmacological treatment, obesity: BMI > 30 kg/m2, lipid disorders requiring implementation of pharmacological treatment in the last 3 months before or during observation, a positive history of ischemic heart disease, carotid atherosclerosis and / or lower limb atherosclerosis, clinically significant arrhythmias or conduction disorders, chronickidney disease, clinically significant liver dysfunction, acute or chronic, clinically manifest inflammatory process, an acute infection in the last month, cancer, taking dietary supplements within a month before inclusion and during observation, taking medication that could interfere with the results of the tests, other conditions that may pose any risk to the patient during the observation.
Facility Information:
Facility Name
Poznan University of Physical Education
City
Poznań
ZIP/Postal Code
61-871
Country
Poland

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
21778224
Citation
Srikanthan P, Karlamangla AS. Relative muscle mass is inversely associated with insulin resistance and prediabetes. Findings from the third National Health and Nutrition Examination Survey. J Clin Endocrinol Metab. 2011 Sep;96(9):2898-903. doi: 10.1210/jc.2011-0435. Epub 2011 Jul 21. Erratum In: J Clin Endocrinol Metab. 2012 Jun;97(6):2203.
Results Reference
background
PubMed Identifier
28879026
Citation
Bird SR, Hawley JA. Update on the effects of physical activity on insulin sensitivity in humans. BMJ Open Sport Exerc Med. 2017 Mar 1;2(1):e000143. doi: 10.1136/bmjsem-2016-000143. eCollection 2016.
Results Reference
background
PubMed Identifier
18511528
Citation
Lambers S, Van Laethem C, Van Acker K, Calders P. Influence of combined exercise training on indices of obesity, diabetes and cardiovascular risk in type 2 diabetes patients. Clin Rehabil. 2008 Jun;22(6):483-92. doi: 10.1177/0269215508084582.
Results Reference
background
PubMed Identifier
28025491
Citation
Oh KJ, Lee DS, Kim WK, Han BS, Lee SC, Bae KH. Metabolic Adaptation in Obesity and Type II Diabetes: Myokines, Adipokines and Hepatokines. Int J Mol Sci. 2016 Dec 22;18(1):8. doi: 10.3390/ijms18010008.
Results Reference
background
PubMed Identifier
30170598
Citation
Ormazabal V, Nair S, Elfeky O, Aguayo C, Salomon C, Zuniga FA. Association between insulin resistance and the development of cardiovascular disease. Cardiovasc Diabetol. 2018 Aug 31;17(1):122. doi: 10.1186/s12933-018-0762-4.
Results Reference
background

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The Effect of 12-week Circuit Training on Insulin Sensitivity and Endothelial Function in Women With Insulin Resistance

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