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Semi-supervised Exercise Program Before Bariatric Surgery

4 juni 2019 bijgewerkt door: Jaime Ruiz-Tovar, MD, PhD, Hospital General Universitario Elche

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.

Studie Overzicht

Toestand

Onbekend

Interventie / Behandeling

Studietype

Ingrijpend

Inschrijving (Verwacht)

60

Fase

  • Niet toepasbaar

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 55 jaar (Volwassen)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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.
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.
Andere namen:
  • Exercise program in patients awaiting bariatric surgery.
Geen tussenkomst: Control group
The control group only will perform the evaluations of the study.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in body composition - Body mass index
Tijdsspanne: Baseline and 3 months, between 8:00 AM and 9:00 AM.
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.
Baseline and 3 months, between 8:00 AM and 9:00 AM.
Change in glucose and HbA1c levels.
Tijdsspanne: Baseline and 3 months, between 8:00 AM and 10:00 AM.
Blood samples will be taken after a 12 h of overnight fast. Exercise will be forbidden 48 h before the test.
Baseline and 3 months, between 8:00 AM and 10:00 AM.
Change in total cholesterol, HDL cholesterol and LDL cholesterol levels.
Tijdsspanne: Baseline and 3 months, between 8:00 AM and 10:00 AM.
Blood samples will be taken after a 12 h of overnight fast. Exercise will be forbidden 48 h before the test.
Baseline and 3 months, between 8:00 AM and 10:00 AM.
Change in systolic and diastolic blood pressure.
Tijdsspanne: Baseline and 3 months, between 8:00 AM and 9:00 AM.
Systolic and Diastolic Blood pressure will be measured according to established recommendations.
Baseline and 3 months, between 8:00 AM and 9:00 AM.
Complications rates
Tijdsspanne: Day 30 after surgery.
All the complications suffered by patients will be recorded.
Day 30 after surgery.
Length of stay.
Tijdsspanne: Day 15 after surgery.
The number of days at hospital after bariatric surgery will be recorded.
Day 15 after surgery.
Change in handgrip strength
Tijdsspanne: Baseline and 3 months, between 5:00 PM and 8:00 PM.
Strength levels will be assessed using a hand dynamometer.
Baseline and 3 months, between 5:00 PM and 8:00 PM.

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in physical activity levels.
Tijdsspanne: Baseline and 3 months, seven days.
Levels of physical activity will be measured recording the physical activity performed for 7 days using an accelerometer.
Baseline and 3 months, seven days.
Change in health-related quality of life: sf-36 questionnaire.
Tijdsspanne: Baseline and 3 months.
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.
Baseline and 3 months.
Change in waist and hip circumference.
Tijdsspanne: Baseline and 3 months, between 8:00 AM and 9:00 AM.
Waist and hip circumference will be measured in centimeters, using established recommendations.
Baseline and 3 months, between 8:00 AM and 9:00 AM.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Verwacht)

1 september 2019

Primaire voltooiing (Verwacht)

31 juli 2020

Studie voltooiing (Verwacht)

30 november 2020

Studieregistratiedata

Eerst ingediend

30 mei 2019

Eerst ingediend dat voldeed aan de QC-criteria

4 juni 2019

Eerst geplaatst (Werkelijk)

5 juni 2019

Updates van studierecords

Laatste update geplaatst (Werkelijk)

5 juni 2019

Laatste update ingediend die voldeed aan QC-criteria

4 juni 2019

Laatst geverifieerd

1 mei 2019

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • HRJC-19_Ex.Bar

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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