Obesity Clinical Trial
Official title:
Effects of Exercise Training on Cardiometabolic Risk Factors and Functional Capacity in Individuals Undergoing Bariatric Surgery
Verified date | January 2023 |
Source | Eastern Mediterranean University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 64 |
Est. completion date | December 1, 2022 |
Est. primary completion date | July 1, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 60 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
Cyprus | Hayriye Tomaç | Famagusta |
Lead Sponsor | Collaborator |
---|---|
Eastern Mediterranean University |
Cyprus,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 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.) |
change from baseline at 8 weeks after the intervention | |
Secondary | 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. |
change from baseline at 8 weeks after the intervention | |
Secondary | Waist and hip circumference | Waist and hip circumference will be measured. Waist / hip circumference ratio will be calculated. | change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | Sorensen Test | Sorensen Test; For trunk extensor muscle endurance | change from baseline at 8 weeks after the intervention | |
Secondary | Trunk Flexor Muscle Endurance Test | Trunk Flexor Muscle Endurance Test; For trunk flexor muscle endurance | change from baseline at 8 weeks after the intervention | |
Secondary | Side Bridge Test (bilateral) | Side Bridge Test (bilateral); For arm muscles providing lateral stability | change from baseline at 8 weeks after the intervention | |
Secondary | Squat Test | Squat Test; It will be applied for lower extremity muscle endurance | change from baseline at 8 weeks after the intervention | |
Secondary | Posture Analysis | Postural evaluation will be carried out using the photographic method. For this purpose, the photograph of the individual will be taken. | change from baseline at 8 weeks after the intervention | |
Secondary | Foot Sense Assessment | Foot sense will be evaluated by light touch and vibration sense measurement. | change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | 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, in 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. |
change from baseline at 8 weeks after the intervention | |
Secondary | 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. |
change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | 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 | change from baseline at 8 weeks after the intervention | |
Secondary | 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 |
change from baseline at 8 weeks after the intervention | |
Secondary | 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. |
change from baseline at 8 weeks after the intervention | |
Secondary | 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. |
change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | 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. . | change from baseline at 8 weeks after the intervention | |
Secondary | 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 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. | change from baseline at 8 weeks after the intervention | |
Secondary | Body weight | Body weight will be evaluated in kg by measuring on a Tanita Brand body analysis monitor (MC-780MA). | change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention | |
Secondary | 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. | change from baseline at 8 weeks after the intervention |
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