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Semi-supervised Exercise Program Before Bariatric Surgery

4. juni 2019 oppdatert av: 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.

Studieoversikt

Status

Ukjent

Intervensjon / Behandling

Studietype

Intervensjonell

Registrering (Forventet)

60

Fase

  • Ikke aktuelt

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 55 år (Voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
Andre navn:
  • Exercise program in patients awaiting bariatric surgery.
Ingen inngripen: Control group
The control group only will perform the evaluations of the study.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in body composition - Body mass index
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 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
Tidsramme: Day 30 after surgery.
All the complications suffered by patients will be recorded.
Day 30 after surgery.
Length of stay.
Tidsramme: Day 15 after surgery.
The number of days at hospital after bariatric surgery will be recorded.
Day 15 after surgery.
Change in handgrip strength
Tidsramme: 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.

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in physical activity levels.
Tidsramme: 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.
Tidsramme: 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.
Tidsramme: 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.

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Forventet)

1. september 2019

Primær fullføring (Forventet)

31. juli 2020

Studiet fullført (Forventet)

30. november 2020

Datoer for studieregistrering

Først innsendt

30. mai 2019

Først innsendt som oppfylte QC-kriteriene

4. juni 2019

Først lagt ut (Faktiske)

5. juni 2019

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

5. juni 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. juni 2019

Sist bekreftet

1. mai 2019

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • HRJC-19_Ex.Bar

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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