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Effects of Exercise Training in Individuals Undergoing Bariatric Surgery

Primary Purpose

Obesity

Status
Completed
Phase
Not Applicable
Locations
Cyprus
Study Type
Interventional
Intervention
Functional Exercise Training Group
Home Exercise Training Group
Sponsored by
Eastern Mediterranean University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity focused on measuring Bariatrics, Obesity, Bariatric Surgery

Eligibility Criteria

20 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Between the ages of 20-60 years,
  • Those who have passed 1 month to 2 years after the operation,
  • Lack of a regular exercise program for the last 6 months (3 and 20 minutes per week.

Exclusion Criteria:

  • Uncontrollable Hypertension (systolic≥160, diastolic≤90 mmHg), Diabetes, Cancer and Cardiovascular Disease
  • Those who have orthopedic, neurological or mental illnesses that prevent them from exercising
  • Previous bariatric surgery
  • Use of drugs that will affect body composition that will cause weight or energy expenditure
  • Having vision, hearing and communication problems

Sites / Locations

  • Hayriye Tomaç

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Functional Exercise Training Group

Home Exercise Training Group

Arm Description

A program including stretching, aerobics, strengthening and balance training will be implemented under the supervision of a physiotherapist with the instructions of the physiotherapist.They will apply a total of 24 sessions of exercise program for 60-80 minutes, 3 days a week, 8 weeks.

Individuals in the home exercise training program will be asked to follow the program in accordance with the home exercise brochure given for 8 weeks, 3 days a week. The program will include stretching, aerobics, strengthening and balance training. The home exercise program will consist of a brochure prepared from a program similar to a functional exercise program.

Outcomes

Primary Outcome Measures

Insulin Resistance
Laboratory tests for the insulin resistance of the individuals will be obtained from the findings that are routinely requested and made by the doctor. For Insulin Resistance; Insulin resistance (HOMA-IR) test will be done by taking a blood test in the laboratory (Blood glucose taken after 8-10 hours of fasting and fasting insulin level will be multiplied by each other and divided by 405 and the insulin resistance level called HOMA-IR will be revealed.)

Secondary Outcome Measures

Body Analysis Monitor
Body composition will be evaluated with the Tanita brand body analysis monitor (MC-780MA). Tanita MC-780 is the multi frequency segmental body composition analyzer. This consists of a stand-alone unit where the subject has to step on barefoot and segmental values will be indicate by the end of the analysis on the digital screen.
Waist and hip circumference
Waist and hip circumference will be measured. Waist / hip circumference ratio will be calculated.
Muscle Strength
A leg and back dynamometer will be used to measure leg and back muscle strength. A hand dynamometer will be used for hand grip strength measurement. Both measurements will be made bilaterally.
Sorensen Test
Sorensen Test; For trunk extensor muscle endurance
Trunk Flexor Muscle Endurance Test
Trunk Flexor Muscle Endurance Test; For trunk flexor muscle endurance
Side Bridge Test (bilateral)
Side Bridge Test (bilateral); For arm muscles providing lateral stability
Squat Test
Squat Test; It will be applied for lower extremity muscle endurance
Posture Analysis
Postural evaluation will be carried out using the photographic method. For this purpose, the photograph of the individual will be taken.
Foot Sense Assessment
Foot sense will be evaluated by light touch and vibration sense measurement.
Time Up & Go Test
This test is an objective, reliable and simple measure of balance and functional movement. It was developed by Podsiadlo and Richardson in 1991. The person will be asked to get up from a seat, walk 3 m, turn around, walk back to the seat and sit. It will be recorded how many seconds he finished the test.
Chair Sit & Go Test
Subjects will be asked to sit in a chair with their hands crossed on their chests. They will be asked to sit up and stand up as fast as possible five times in a row. The test will be started in sitting position and the test will be terminated at the last take-off. The time in seconds will be kept. The test will be performed 2 times and the best score will be recorded.
Normal walking speed
For normal walking, the person will be asked to walk a distance of 4 meters at a normal pace as in daily life, and the time to walk the 4 meters distance will be calculated in seconds. The test will be performed 2 times and the best score will be recorded.
Fast walking speed
For fast walking, the person will be asked to walk a distance of 4 meters as fast as possible. The test will be done only once and the achieved grade will be recorded. Normal walking and fast walking speed will be recorded in m/s by dividing the distance by the recorded times.
One Foot Stand Test
The time in seconds for individuals to stand on one leg, without shoes, by supporting their hands on their waists and bending their knees will be recorded. It will be done 2 times for each leg and the best score will be recorded.
Total physical capacity score
As a result of the tests, the total physical capacity score will be obtained. Individuals '' Timed Up & Go Test (sec), Chair Sit & Go Test (sec), normal (m / sec) and fast walking speed (m / sec) and One Foot Stand Test (right / left average, sec) '' will be applied.
Balance
Lower extremity Y balance test will be applied for Dynamic Balance. For Static Balance, eyes will be evaluated with open and closed eyes on one leg.
Short-Form Mcgill Pain Questionnaire
Pain will be assessed by the Short-Form Mcgill Pain Questionnaire (SF-MAA). This form provides information about perceptual, sensory and severity components in pain perception. 15 descriptive adjectives (11 sensory and 4 affective) are used to determine the perception of pain. Descriptive adjectives in the pain perception of the cases are evaluated with a numerical value scale (0 = absent, 1 = mild, 2 = moderate, 3 = severe). In addition, ın this form have a visual analog scale of 10 cm is used to measure the pain intensity felt during the evaluation. They will be asked to indicate the pain they felt during the evaluation with an "X" mark on a 10 cm scale. According to this scale, a value of "0" indicates no pain, and "10" indicates the most severe pain. The distance between the marked point and the starting point is measured in cm.
Visual Analog Scale
Visual analog scale of 10 cm is used to measure the pain intensity felt during the evaluation. They will be asked to indicate the pain they felt during the evaluation with an "X" mark on a 10 cm scale. According to this scale, a value of "0" indicates no pain, and "10" indicates the most severe pain. The distance between the marked point and the starting point is measured in cm. Accordingly, 0 means no pain, 10 means the most unbearable pain. Pain intensity increases as go to 10.
Exercise Benefits Barriers
Exercise Benefits Barriers Scale will be evaluated to determine exercise benefit and obstacle perceptions of obese women.The scale is evaluated over the total score (min=24, max= 96). Higher scores indicate perceived greater exercise benefits and fewer exercise barriers.
Exercise Self-Efficacy
With Exercise Self-Efficacy Scale, questions will be asked to measure the self-efficacy of obese women in exercising.A high total score from the scale indicates that the individual's self-efficacy perception is at a good level.
Exercise Beliefs
Obese women will be asked to score according to the VAS scale to determine their physical activity beliefs. According to the VAS scale by asking the question "How important is physical activity for you?" It will be asked to mark on the scale. Accordingly, a score between 0 and 10 is made. 0 means no pain, 10 means the most unbearable pain. Pain intensity increases as go to 10
Self respect
The Rosenberg Self-Esteem Scale will be used to evaluate the self-esteem of individuals. Low score in scale scoring means high self-esteem; a high score indicates low self-esteem. 0-1 points as high self-esteem, 2-4 points as medium self-esteem, 5-6 points as low self-esteem
Body Image
Body Image Scale will be used to evaluate the body image satisfaction level of individuals. The most positive statement gets 5 points, and the most negative statement gets 1 point. An increase in the total score obtained from the scale indicates an increase in satisfaction with one's body parts or function, and a decrease in a score indicates a decrease in satisfaction.
Life quality
Obesity Specific Quality of Life Scale will be used to assess the quality of life. As the total score from the scale approaches 0, the quality of life decreases, and as it approaches 100, the quality of life increases.
Functional Exercise Capacity
Six Minute Walk Test will be applied. The Six Minute Walk Test is a submaximal exercise test that evaluates exercise tolerance and exercise-related cardiorespiratory changes.
Lipid Profile
Laboratory tests for the lipid profile of the individuals will be obtained from the findings that are routinely requested and made by the doctor. For this, blood findings will be taken in the analysis laboratory. For Lipid Profile; Triglycerides (TG), High-density lipoprotein cholesterol (HDL-C), Low-density lipoprotein cholesterol (LDL-C), Total cholesterol (TC), Glucose, Glycosylated Hemoglobin (HbA1c), C Reactive Protein (CRP) values will be checked in the results of blood tests. .
İnsulin Resistance
Laboratory tests for the insulin resistance of the individuals will be obtained from the findings that are routinely requested and made by the doctor. For this, blood findings will be taken in the analysis laboratory. Insulin resistance test; The blood glucose taken after 8-10 hours of fasting will be multiplied by the fasting insulin level and divided by 405 and the insulin resistance level called HOMA-IR will appear. In this test, it will be checked as a result of blood tests to be taken in the laboratory.
Body weight
Body weight will be evaluated in kg by measuring on a Tanita Brand body analysis monitor (MC-780MA).
Height
Height is measured without shoes, heavy outer garments and hair ornaments. The back of the head, shoulder blades, buttocks and heels are touching the tape measure attached to the wall.The value in cm is taken.
Body mass index
The Body Mass Index measurement will be obtained by dividing the weight in kilograms by the square of the height in meters (kg/m²) to arrive at a single reported value.

Full Information

First Posted
May 24, 2021
Last Updated
January 16, 2023
Sponsor
Eastern Mediterranean University
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1. Study Identification

Unique Protocol Identification Number
NCT05085015
Brief Title
Effects of Exercise Training in Individuals Undergoing Bariatric Surgery
Official Title
Effects of Exercise Training on Cardiometabolic Risk Factors and Functional Capacity in Individuals Undergoing Bariatric Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Completed
Study Start Date
December 10, 2021 (Actual)
Primary Completion Date
July 1, 2022 (Actual)
Study Completion Date
December 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Eastern Mediterranean University

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
The subject of the research; Effects of exercise training on cardiometabolic risk factors and functional capacity in individuals undergoing bariatric surgery. Purpose of the research; Cardiometabolic risk factors, body composition, muscle strength and endurance, posture, foot sense, physical exercise capacity, balance, pain, exercise benefits - barriers, exercise self-efficacy, exercise beliefs, to evaluate the effects on body esteem, body image and quality of life. Method of Research: Post-surgical interventions are important in individuals who have undergone bariatric surgery. Intervention programs that include exercise, encourage the change in the lifestyle of individuals, effectively and accurately reduce post-surgical obesity. Functional Exercise Training, which can also be used for obesity treatment, consists of stretching, aerobics, strengthening and balance training. Therefore, it has a positive effect on body systems. In addition, Home Exercise Training can be used within the scope of obesity treatment. Exercise is one of the alternative methods by providing the adaptation of the individual to the exercise. Socio-demographic and physical characteristics of individuals will be recorded. Laboratory tests will be ordered for cardiometabolic risk factors. Body composition will be determined by Tanita brand body analysis monitor (MC-780MA). Posture will be evaluated by photogrammetry technique. Muscle strength assessment will be evaluated by leg, back and hand dynamometer instrument, muscle endurance tests, sensory assessment by foot sense assessment, physical capacity with physical exercise capacity tests, balance static and dynamic balance tests and pain questionnaire. Exercise benefits-barriers will be assessed by Exercise Benefits Barriers Scale, exercise self-efficacy by Exercise Self-Efficacy Scale. Exercise beliefs will also be questioned with a questionnaire. Self-esteem will be evaluated for all groups before and after treatment. The self respect will be evaluated by using the Rosenberg Self-Esteem Scale, body image with the Body Image Scale, with the quality of life using the Obesity-Specific Quality of Life Scale.The training will be carried out 3 days a week for 8 weeks, approximately 1 hour. Sufficient number of assessments and exercises will be used for individuals to become familiar with the equipment and training protocol.
Detailed Description
Obesity is defined as abnormal or excessive fat accumulation in the body to the extent that it disrupts health. The prevalence of obesity is increasing day by day in developed and developing countries. While 600 million of the world population were obese in 2014, this situation reached 700 million in 2015, and when the trend continues in the same way, it is thought that more than 3 billion people will have overweight or obesity in 2030. Therefore, the worldwide prevalence of morbid obesity will increase rapidly. Obesity is a risk factor especially for cardiovascular disease and causes an increase in mortality and morbidity with the central accumulation of adipose tissues. It affects the muscle, liver, subcutaneous and intra-abdominal regions, especially due to intraabdominal and / or visceral fat. As a result, cardiometabolic complications occur, as it causes physical inactivity, muscle strength and endurance are affected, posture is affected, physical performance is affected, self-esteem, body image, health-related quality of life and exercise avoidance occur. It has been reported that approximately 91% of obese individuals complain of musculoskeletal pain, 69% of them have back pain and 58% have knee pain. When the literature is examined, it is seen that conservative therapies such as nutrition, exercise and drug management are used intensively in the treatment of obesity, more invasive methods are more prominent today and bariatric surgery is preferred by many people. Studies emphasize that non-surgical methods fail to achieve permanent success compared to surgical methods. Obese individuals undergoing bariatric surgery have reported a large diet history that failed to stop weight gain, starting in adolescence. It has been reported that obese individuals experience higher levels of symptoms such as stress, anxiety, depression, food cravings and psychological effects such as lower self-esteem compared to normal weight individuals, and this situation continuously increases weight gain. For this reason, bariatric surgery has become increasingly common in the fight for effective weight loss. The postoperative process in which exercise and lifestyle changes are adopted after bariatric surgery is important. With the prominence of bariatric surgery in the studies performed, if weight loss management is not planned well after surgery, weight gain and complications occur after surgery, and it is seen that the effect of the surgery performed decreases. Weight recovery in this population also increases the likelihood of the return of obesity-related comorbidities. Insufficient physical activity and inadequate nutritional support after surgery cause sarcopenia. Therefore, it is an important anabolic stimulant for the prevention of muscle protein synthesis and sarcopenia formation, together with adequate nutritional support, together with early physical activity after surgery. Increasing physical activity, exercise and lifestyle changes are important in maintaining the weight given during the postoperative period, reducing muscle loss and increasing fat burning. The purposes of exercise training given in the post-surgery period in obese individuals are to increase body fat mass loss, protect muscle mass, and improve physical and mental health. Although there are studies in which exercise training is important following bariatric surgery, there is insufficient evidence regarding the interventions of different exercise protocols. Finding the best exercise protocols, increasing body fat mass loss and preserving muscle mass is important as part of the post-surgical guideline. Studies have reported that physical exercise is a positive predictor of outcome after bariatric surgery. Intervention programs that include exercise are reported to effectively reduce obesity and comorbidity by encouraging individuals to change their lifestyle after such surgery. Studies have shown that exercise is considered an effective mediator for correcting insulin resistance, effectively reduces indicators of obesity such as body mass index (BMI) and body fat percentage, and reduced risk factors for cardiovascular diseases. Therefore, the main purpose of the study is to evaluate the effects of exercise training on cardiometabolic risk factors and functional capacity in individuals who have undergone bariatric surgery. There is no such exercise protocol study conducted in Cyprus. The investigators are of the opinion that the research is an interesting study in this respect. Functional Exercise Training is a type of exercise that includes training for stretching, aerobics, strengthening and balance. Studies on obese individuals have reported a positive effect on body composition, functional capacity and quality of life. Home Exercise Training, on the other hand, is one of the alternative methods of exercise that maximizes the sustainability of behavioral change by providing adaptation to exercise throughout life. It is an option that will increase an individual's physical activity compliance. Evidence regarding the effectiveness of Functional Exercise Training and Home Exercise Training in Individuals Undergoing Bariatric Surgery is insufficient and it is necessary to know and clarify the differences create. It is necessary to clarify whether individuals continue the exercise in their daily lives and whether the continuity of the effects of the exercise should be addressed. In this context, the content and effects of the exercise programs to be applied to individuals who have undergone bariatric surgery are important in Cyprus for future multifactorial situations and may guide individuals.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity
Keywords
Bariatrics, Obesity, Bariatric Surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Functional Exercise Training Group
Arm Type
Experimental
Arm Description
A program including stretching, aerobics, strengthening and balance training will be implemented under the supervision of a physiotherapist with the instructions of the physiotherapist.They will apply a total of 24 sessions of exercise program for 60-80 minutes, 3 days a week, 8 weeks.
Arm Title
Home Exercise Training Group
Arm Type
Experimental
Arm Description
Individuals in the home exercise training program will be asked to follow the program in accordance with the home exercise brochure given for 8 weeks, 3 days a week. The program will include stretching, aerobics, strengthening and balance training. The home exercise program will consist of a brochure prepared from a program similar to a functional exercise program.
Intervention Type
Other
Intervention Name(s)
Functional Exercise Training Group
Intervention Description
Training will start with Stretching Training and end with stretching training. Stretching exercises targeting actively applied shoulder girdle, chest, neck, trunk, hip, front and back leg and ankle muscle groups will be given. Afterwards, it will be continued with Aerobic Exercise Training. The training will be given on the treadmill "Treadmill Technogym". Afterwards, it will be continued with Strengthening Training. Strength training will consist of a strengthening program that includes the lower extremity, upper extremity, trunk and core region. Elastic bands will be used in the training. Then, balance training will be given at the end.
Intervention Type
Other
Intervention Name(s)
Home Exercise Training Group
Intervention Description
Training will start with Stretching Training and end with stretching training. Stretching exercises targeting actively applied shoulder girdle, chest, neck, trunk, hip, front and back leg and ankle muscle groups will be given. Afterwards, it will be continued with Aerobic Exercise Training. They will walk at least 30 minutes, 3 days a week for 8 weeks at outdoor. Afterwards, it will be continued with Strengthening Training. Strength training will consist of a strengthening program that includes the lower extremity, upper extremity, trunk and core region. Elastic bands will be used in the training. Then, balance training will be given at the end.
Primary Outcome Measure Information:
Title
Insulin Resistance
Description
Laboratory tests for the insulin resistance of the individuals will be obtained from the findings that are routinely requested and made by the doctor. For Insulin Resistance; Insulin resistance (HOMA-IR) test will be done by taking a blood test in the laboratory (Blood glucose taken after 8-10 hours of fasting and fasting insulin level will be multiplied by each other and divided by 405 and the insulin resistance level called HOMA-IR will be revealed.)
Time Frame
change from baseline at 8 weeks after the intervention
Secondary Outcome Measure Information:
Title
Body Analysis Monitor
Description
Body composition will be evaluated with the Tanita brand body analysis monitor (MC-780MA). Tanita MC-780 is the multi frequency segmental body composition analyzer. This consists of a stand-alone unit where the subject has to step on barefoot and segmental values will be indicate by the end of the analysis on the digital screen.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Waist and hip circumference
Description
Waist and hip circumference will be measured. Waist / hip circumference ratio will be calculated.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Muscle Strength
Description
A leg and back dynamometer will be used to measure leg and back muscle strength. A hand dynamometer will be used for hand grip strength measurement. Both measurements will be made bilaterally.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Sorensen Test
Description
Sorensen Test; For trunk extensor muscle endurance
Time Frame
change from baseline at 8 weeks after the intervention
Title
Trunk Flexor Muscle Endurance Test
Description
Trunk Flexor Muscle Endurance Test; For trunk flexor muscle endurance
Time Frame
change from baseline at 8 weeks after the intervention
Title
Side Bridge Test (bilateral)
Description
Side Bridge Test (bilateral); For arm muscles providing lateral stability
Time Frame
change from baseline at 8 weeks after the intervention
Title
Squat Test
Description
Squat Test; It will be applied for lower extremity muscle endurance
Time Frame
change from baseline at 8 weeks after the intervention
Title
Posture Analysis
Description
Postural evaluation will be carried out using the photographic method. For this purpose, the photograph of the individual will be taken.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Foot Sense Assessment
Description
Foot sense will be evaluated by light touch and vibration sense measurement.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Time Up & Go Test
Description
This test is an objective, reliable and simple measure of balance and functional movement. It was developed by Podsiadlo and Richardson in 1991. The person will be asked to get up from a seat, walk 3 m, turn around, walk back to the seat and sit. It will be recorded how many seconds he finished the test.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Chair Sit & Go Test
Description
Subjects will be asked to sit in a chair with their hands crossed on their chests. They will be asked to sit up and stand up as fast as possible five times in a row. The test will be started in sitting position and the test will be terminated at the last take-off. The time in seconds will be kept. The test will be performed 2 times and the best score will be recorded.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Normal walking speed
Description
For normal walking, the person will be asked to walk a distance of 4 meters at a normal pace as in daily life, and the time to walk the 4 meters distance will be calculated in seconds. The test will be performed 2 times and the best score will be recorded.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Fast walking speed
Description
For fast walking, the person will be asked to walk a distance of 4 meters as fast as possible. The test will be done only once and the achieved grade will be recorded. Normal walking and fast walking speed will be recorded in m/s by dividing the distance by the recorded times.
Time Frame
change from baseline at 8 weeks after the intervention
Title
One Foot Stand Test
Description
The time in seconds for individuals to stand on one leg, without shoes, by supporting their hands on their waists and bending their knees will be recorded. It will be done 2 times for each leg and the best score will be recorded.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Total physical capacity score
Description
As a result of the tests, the total physical capacity score will be obtained. Individuals '' Timed Up & Go Test (sec), Chair Sit & Go Test (sec), normal (m / sec) and fast walking speed (m / sec) and One Foot Stand Test (right / left average, sec) '' will be applied.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Balance
Description
Lower extremity Y balance test will be applied for Dynamic Balance. For Static Balance, eyes will be evaluated with open and closed eyes on one leg.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Short-Form Mcgill Pain Questionnaire
Description
Pain will be assessed by the Short-Form Mcgill Pain Questionnaire (SF-MAA). This form provides information about perceptual, sensory and severity components in pain perception. 15 descriptive adjectives (11 sensory and 4 affective) are used to determine the perception of pain. Descriptive adjectives in the pain perception of the cases are evaluated with a numerical value scale (0 = absent, 1 = mild, 2 = moderate, 3 = severe). In addition, ın this form have a visual analog scale of 10 cm is used to measure the pain intensity felt during the evaluation. They will be asked to indicate the pain they felt during the evaluation with an "X" mark on a 10 cm scale. According to this scale, a value of "0" indicates no pain, and "10" indicates the most severe pain. The distance between the marked point and the starting point is measured in cm.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Visual Analog Scale
Description
Visual analog scale of 10 cm is used to measure the pain intensity felt during the evaluation. They will be asked to indicate the pain they felt during the evaluation with an "X" mark on a 10 cm scale. According to this scale, a value of "0" indicates no pain, and "10" indicates the most severe pain. The distance between the marked point and the starting point is measured in cm. Accordingly, 0 means no pain, 10 means the most unbearable pain. Pain intensity increases as go to 10.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Exercise Benefits Barriers
Description
Exercise Benefits Barriers Scale will be evaluated to determine exercise benefit and obstacle perceptions of obese women.The scale is evaluated over the total score (min=24, max= 96). Higher scores indicate perceived greater exercise benefits and fewer exercise barriers.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Exercise Self-Efficacy
Description
With Exercise Self-Efficacy Scale, questions will be asked to measure the self-efficacy of obese women in exercising.A high total score from the scale indicates that the individual's self-efficacy perception is at a good level.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Exercise Beliefs
Description
Obese women will be asked to score according to the VAS scale to determine their physical activity beliefs. According to the VAS scale by asking the question "How important is physical activity for you?" It will be asked to mark on the scale. Accordingly, a score between 0 and 10 is made. 0 means no pain, 10 means the most unbearable pain. Pain intensity increases as go to 10
Time Frame
change from baseline at 8 weeks after the intervention
Title
Self respect
Description
The Rosenberg Self-Esteem Scale will be used to evaluate the self-esteem of individuals. Low score in scale scoring means high self-esteem; a high score indicates low self-esteem. 0-1 points as high self-esteem, 2-4 points as medium self-esteem, 5-6 points as low self-esteem
Time Frame
change from baseline at 8 weeks after the intervention
Title
Body Image
Description
Body Image Scale will be used to evaluate the body image satisfaction level of individuals. The most positive statement gets 5 points, and the most negative statement gets 1 point. An increase in the total score obtained from the scale indicates an increase in satisfaction with one's body parts or function, and a decrease in a score indicates a decrease in satisfaction.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Life quality
Description
Obesity Specific Quality of Life Scale will be used to assess the quality of life. As the total score from the scale approaches 0, the quality of life decreases, and as it approaches 100, the quality of life increases.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Functional Exercise Capacity
Description
Six Minute Walk Test will be applied. The Six Minute Walk Test is a submaximal exercise test that evaluates exercise tolerance and exercise-related cardiorespiratory changes.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Lipid Profile
Description
Laboratory tests for the lipid profile of the individuals will be obtained from the findings that are routinely requested and made by the doctor. For this, blood findings will be taken in the analysis laboratory. For Lipid Profile; Triglycerides (TG), High-density lipoprotein cholesterol (HDL-C), Low-density lipoprotein cholesterol (LDL-C), Total cholesterol (TC), Glucose, Glycosylated Hemoglobin (HbA1c), C Reactive Protein (CRP) values will be checked in the results of blood tests. .
Time Frame
change from baseline at 8 weeks after the intervention
Title
İnsulin Resistance
Description
Laboratory tests for the insulin resistance of the individuals will be obtained from the findings that are routinely requested and made by the doctor. For this, blood findings will be taken in the analysis laboratory. Insulin resistance test; The blood glucose taken after 8-10 hours of fasting will be multiplied by the fasting insulin level and divided by 405 and the insulin resistance level called HOMA-IR will appear. In this test, it will be checked as a result of blood tests to be taken in the laboratory.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Body weight
Description
Body weight will be evaluated in kg by measuring on a Tanita Brand body analysis monitor (MC-780MA).
Time Frame
change from baseline at 8 weeks after the intervention
Title
Height
Description
Height is measured without shoes, heavy outer garments and hair ornaments. The back of the head, shoulder blades, buttocks and heels are touching the tape measure attached to the wall.The value in cm is taken.
Time Frame
change from baseline at 8 weeks after the intervention
Title
Body mass index
Description
The Body Mass Index measurement will be obtained by dividing the weight in kilograms by the square of the height in meters (kg/m²) to arrive at a single reported value.
Time Frame
change from baseline at 8 weeks after the intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Between the ages of 20-60 years, Those who have passed 1 month to 2 years after the operation, Lack of a regular exercise program for the last 6 months (3 and 20 minutes per week. Exclusion Criteria: Uncontrollable Hypertension (systolic≥160, diastolic≤90 mmHg), Diabetes, Cancer and Cardiovascular Disease Those who have orthopedic, neurological or mental illnesses that prevent them from exercising Previous bariatric surgery Use of drugs that will affect body composition that will cause weight or energy expenditure Having vision, hearing and communication problems
Facility Information:
Facility Name
Hayriye Tomaç
City
Famagusta
ZIP/Postal Code
99450
Country
Cyprus

12. IPD Sharing Statement

Plan to Share IPD
Yes

Learn more about this trial

Effects of Exercise Training in Individuals Undergoing Bariatric Surgery

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