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Calorie Restriction, Protein Supplementation and Metabolic Health (CRPS)

22. marts 2017 opdateret af: Washington University School of Medicine

Calorie Restriction and Metabolic Health

The purpose of this study is to determine whether consuming additional protein during calorie restriction induced weight loss has beneficial or harmful effects on multi-organ (liver, muscle, adipose tissue) insulin sensitivity, colonocyte proliferation rates, the gut microbiome, muscle mass and function, and bone mineral density in obese, postmenopausal women.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

75

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Missouri
      • Saint Louis, Missouri, Forenede Stater, 63110
        • Washington University School of Medicine

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

50 år til 65 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Kvinde

Beskrivelse

Inclusion Criteria:

  • Obese with body mass index (BMI) between 30 and 50 kg/m2
  • Postmenopausal
  • Sedentary (i.e., less than 1.5 hours of exercise per week)

Exclusion Criteria:

  • Individuals with diabetes and/or uncontrolled hypertension
  • Individuals with hepatitis B and/or C
  • Individuals who smoke
  • Individuals with an allergy to whey protein

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: Vægttab med normalt proteinindtag
Goal of 8 to 10% weight loss while consuming the recommended daily allowance of protein (i.e, 0.8 grams of protein per kg body weight per day).
Ingen indgriben: Weight maintenance
Weight maintenance with normal protein intake
Eksperimentel: Weight loss with protein supplementation
Goal of 8 to 10% weight loss while consuming 150% of the recommended daily allowance of protein (i.e., 1.2 grams of protein per kg body weight per day).

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in muscle volume
Tidsramme: Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
Thigh muscle volume will be measured by magnetic resonance imaging (MRI)
Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
Change in muscle strength
Tidsramme: Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
Muscle strength will be evaluated by administering maximum one repetition strength and isokinetic strength tests.
Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
Changes in bone mineral density and bone mineral content
Tidsramme: Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
Total bone mass and total body and regional bone mineral density will be evaluated by using dual X-ray energy absorptiometry (DXA).
Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Ændring i bakteriepopulationer fundet i afføringen
Tidsramme: Baseline og ved 10 % vægttab i kaloriebegrænsende grupper og ~6 til 7 måneder i vægtvedligeholdelsesgruppen
Baseline og ved 10 % vægttab i kaloriebegrænsende grupper og ~6 til 7 måneder i vægtvedligeholdelsesgruppen
Change in insulin sensitivity
Tidsramme: Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
Insulin sensitivity (glucose rate of disappearance [Rd] during a hyperinsulinemic-euglycemic clamp procedure) will be evaluated in a subset of 10 participants per group because power analysis has determined that this number is sufficient to detect a 25% difference between groups assuming 80% power, an alpha value of 0.05 and an average baseline insulin-stimulated glucose Rd of 2,590 ± 492 µmol/min, the average ± SD insulin stimulated glucose Rd the investigators have measured during the past 20 y in obese subjects. In the investigators' experience (Kirk et al., 2009 and Magkos et al., 2016), the weight loss induced increase in insulin stimulated glucose Rd is ~50%.
Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
Change in muscle protein metabolism
Tidsramme: Baseline and at 5% weight loss in the calorie restriction groups and after ~3 months in the weight maintenance group
Rates of muscle protein synthesis, breakdown and net protein balance will be assessed during postabsorptive conditions and when insulin and/or amino acid concentrations are elevated.
Baseline and at 5% weight loss in the calorie restriction groups and after ~3 months in the weight maintenance group
Change in cell proliferation (growth) rates in the colon
Tidsramme: Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
Colon cell proliferation rates will be determined using stable isotope labelled tracer methods in conjunction with sigmoid colon biopsy samples
Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
Determine the acute effect of whey protein ingestion on skeletal muscle insulin sensitivity
Tidsramme: Prior to starting the weight loss or maintenance intervention
Insulin sensitivity will be evaluated using the hyperinsulinemic-euglycemic clamp procedure in conjunction with stable isotope labeled tracer infusions
Prior to starting the weight loss or maintenance intervention
Determine the acute effect of whey protein ingestion on muscle protein metabolism
Tidsramme: Prior to starting the weight loss or maintenance intervention
Rates of muscle protein synthesis, breakdown and net protein balance will be assessed using stable isotope labeled tracer methods during postabsorptive conditions and during insulin infusion with or without whey protein ingestion
Prior to starting the weight loss or maintenance intervention

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

1. januar 2012

Primær færdiggørelse (Faktiske)

1. marts 2017

Studieafslutning (Faktiske)

1. marts 2017

Datoer for studieregistrering

Først indsendt

20. februar 2012

Først indsendt, der opfyldte QC-kriterier

20. februar 2012

Først opslået (Skøn)

24. februar 2012

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

27. marts 2017

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

22. marts 2017

Sidst verificeret

1. marts 2017

Mere information

Begreber relateret til denne undersøgelse

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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