Semi-supervised Exercise Program Before Bariatric Surgery
Effects of Exercise on Body Composition, Cardiovascular Risk Factors and Surgery Complications in Bariatric Patients
Background: Patients awaiting bariatric surgery, apart from suffering higher BMI, show a large number of comorbidities and a low physical fitness. These factors are associated with a longer surgery time, a longer hospital stay and a greater number of operative complications. To reduce these disadvantages, a nutritional intervention is performed to reduce total weight and the comorbidities associated with obesity prior to surgery. However, the prescription of an exercise program, which can be an effective tool to improve these factors, is not usually part of the usual care of these patients.
Objective: To know the effects of a semi-supervised exercise program on body composition, cardiovascular risk factors and operative complications in bariatric patients.
Methods: Approximately 3 months before surgery, 60 patients awaiting bariatric surgery will be recruited. Patients will be randomized into two groups: a) an experimental group (n = 30); b) a control group (n = 30). The experimental group will perform a semi-supervised exercise program, while the control group will only perform the corresponding evaluations. Both groups will be assessed for body composition, cardiovascular risk factors, physical condition, quality of life and physical activity levels at the beginning and at the end of the intervention. In addition, surgery time, hospital length of stay and operative complications will be evaluated in both groups.
연구 개요
연구 유형
등록 (예상)
단계
- 해당 없음
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Age between 20-55 years.
- All patients awaiting bariatric surgery.
Exclusion Criteria:
- Patients with chronic respiratory diseases
- Patients with cardiovascular diseases
- Inability to perform exercise
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
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실험적: Exercise group
Three months of semi-supervised exercise program in patients awaiting bariatric surgery.
Body composition, cardiovascular risk factors, physical fitness, physical activity levels and quality of life will be assessed before and at the end of the study.
In addition, surgery time, hospital length of stay and operative complications also will be evaluated.
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Twelve-week of semi-supervised exercise program.
The exercise program will combine resistance and endurance training.
Both the volume and intensity of training will start at moderate intensity, and progressively be increased at higher volumes and intensities.
다른 이름들:
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간섭 없음: Control group
The control group only will perform the evaluations of the study.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
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Change in body composition - Body mass index
기간: Baseline and 3 months, between 8:00 AM and 9:00 AM.
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Bioimpedance analysis will be used for establishing body weight and body composition.
This variables will be evaluated between 8:00 and 9:00 A.M., after at least 8 hours of fasting, with an empty bladder.
Body mass index will be calculated dividing weight in kilograms by squared height in meters.
Therefore, body mass index will be expressed as kg·m-2.
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Baseline and 3 months, between 8:00 AM and 9:00 AM.
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Change in glucose and HbA1c levels.
기간: Baseline and 3 months, between 8:00 AM and 10:00 AM.
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Blood samples will be taken after a 12 h of overnight fast.
Exercise will be forbidden 48 h before the test.
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Baseline and 3 months, between 8:00 AM and 10:00 AM.
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Change in total cholesterol, HDL cholesterol and LDL cholesterol levels.
기간: Baseline and 3 months, between 8:00 AM and 10:00 AM.
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Blood samples will be taken after a 12 h of overnight fast.
Exercise will be forbidden 48 h before the test.
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Baseline and 3 months, between 8:00 AM and 10:00 AM.
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Change in systolic and diastolic blood pressure.
기간: Baseline and 3 months, between 8:00 AM and 9:00 AM.
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Systolic and Diastolic Blood pressure will be measured according to established recommendations.
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Baseline and 3 months, between 8:00 AM and 9:00 AM.
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Complications rates
기간: Day 30 after surgery.
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All the complications suffered by patients will be recorded.
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Day 30 after surgery.
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Length of stay.
기간: Day 15 after surgery.
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The number of days at hospital after bariatric surgery will be recorded.
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Day 15 after surgery.
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Change in handgrip strength
기간: Baseline and 3 months, between 5:00 PM and 8:00 PM.
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Strength levels will be assessed using a hand dynamometer.
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Baseline and 3 months, between 5:00 PM and 8:00 PM.
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Change in physical activity levels.
기간: Baseline and 3 months, seven days.
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Levels of physical activity will be measured recording the physical activity performed for 7 days using an accelerometer.
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Baseline and 3 months, seven days.
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Change in health-related quality of life: sf-36 questionnaire.
기간: Baseline and 3 months.
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The Spanish version of Short Form Health Survey 36 (SF-36) will be used for knowing changes in quality of life.
This questionnaire uses 8 scales to evaluate physical health (4 scales: Physical Function, Role Physical, Bodily Pain, General Health) and mental health (4 scales: Vitality, Social functioning, Role Emotional, and Mental Health).
The scores of these scales are transformed into values between 0-100 points, where highest scores are related to better function.
These 8 scales are grouped into two summary components (physical summary component; mental summary component) which will be calculated according to the reference values of the Spanish population, with a mean of 50 and standard deviation of 10.population.
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Baseline and 3 months.
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Change in waist and hip circumference.
기간: Baseline and 3 months, between 8:00 AM and 9:00 AM.
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Waist and hip circumference will be measured in centimeters, using established recommendations.
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Baseline and 3 months, between 8:00 AM and 9:00 AM.
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (예상)
기본 완료 (예상)
연구 완료 (예상)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .