- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01538836
Calorie Restriction, Protein Supplementation and Metabolic Health (CRPS)
22. mars 2017 oppdatert av: 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.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
75
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Missouri
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Saint Louis, Missouri, Forente stater, 63110
- Washington University School of Medicine
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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
50 år til 65 år (Voksen, Eldre voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Hunn
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
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 |
|---|---|
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Aktiv komparator: Vekttap med normalt proteininntak
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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).
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Ingen inngripen: Weight maintenance
Weight maintenance with normal protein intake
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Eksperimentell: Weight loss with protein supplementation
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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).
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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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
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Thigh muscle volume will be measured by magnetic resonance imaging (MRI)
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Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
|
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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
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Muscle strength will be evaluated by administering maximum one repetition strength and isokinetic strength tests.
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Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
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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
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Total bone mass and total body and regional bone mineral density will be evaluated by using dual X-ray energy absorptiometry (DXA).
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Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Endring i bakteriepopulasjoner funnet i avføringen
Tidsramme: Baseline og ved 10 % vekttap i kalorirestriksjonsgrupper og ~6 til 7 måneder i vektvedlikeholdsgruppen
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Baseline og ved 10 % vekttap i kalorirestriksjonsgrupper og ~6 til 7 måneder i vektvedlikeholdsgruppen
|
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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
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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%.
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Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
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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
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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.
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Baseline and at 5% weight loss in the calorie restriction groups and after ~3 months in the weight maintenance group
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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
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Colon cell proliferation rates will be determined using stable isotope labelled tracer methods in conjunction with sigmoid colon biopsy samples
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Baseline and at 10% weight loss in calorie restriction groups and ~6 to 7 months in the weight maintenance group
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Determine the acute effect of whey protein ingestion on skeletal muscle insulin sensitivity
Tidsramme: Prior to starting the weight loss or maintenance intervention
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Insulin sensitivity will be evaluated using the hyperinsulinemic-euglycemic clamp procedure in conjunction with stable isotope labeled tracer infusions
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Prior to starting the weight loss or maintenance intervention
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Determine the acute effect of whey protein ingestion on muscle protein metabolism
Tidsramme: Prior to starting the weight loss or maintenance intervention
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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
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Prior to starting the weight loss or maintenance intervention
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Samarbeidspartnere
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Generelle publikasjoner
- Kirk E, Reeds DN, Finck BN, Mayurranjan SM, Patterson BW, Klein S. Dietary fat and carbohydrates differentially alter insulin sensitivity during caloric restriction. Gastroenterology. 2009 May;136(5):1552-60. doi: 10.1053/j.gastro.2009.01.048. Epub 2009 Jan 25. Erratum In: Gastroenterology. 2009 Jul;137(1):393. Mayurranjan, Mitra S [corrected to Mayurranjan S Mitra].
- Smith GI, Yoshino J, Stromsdorfer KL, Klein SJ, Magkos F, Reeds DN, Klein S, Mittendorfer B. Protein Ingestion Induces Muscle Insulin Resistance Independent of Leucine-Mediated mTOR Activation. Diabetes. 2015 May;64(5):1555-63. doi: 10.2337/db14-1279. Epub 2014 Dec 4.
- Harris LLS, Smith GI, Patterson BW, Ramaswamy RS, Okunade AL, Kelly SC, Porter LC, Klein S, Yoshino J, Mittendorfer B. Alterations in 3-Hydroxyisobutyrate and FGF21 Metabolism Are Associated With Protein Ingestion-Induced Insulin Resistance. Diabetes. 2017 Jul;66(7):1871-1878. doi: 10.2337/db16-1475. Epub 2017 May 4.
- Magkos F, Bradley D, Eagon JC, Patterson BW, Klein S. Effect of Roux-en-Y gastric bypass and laparoscopic adjustable gastric banding on gastrointestinal metabolism of ingested glucose. Am J Clin Nutr. 2016 Jan;103(1):61-5. doi: 10.3945/ajcn.115.116111. Epub 2015 Nov 25.
- Smith GI, Yoshino J, Kelly SC, Reeds DN, Okunade A, Patterson BW, Klein S, Mittendorfer B. High-Protein Intake during Weight Loss Therapy Eliminates the Weight-Loss-Induced Improvement in Insulin Action in Obese Postmenopausal Women. Cell Rep. 2016 Oct 11;17(3):849-861. doi: 10.1016/j.celrep.2016.09.047.
- Smith GI, Patterson BW, Klein SJ, Mittendorfer B. Effect of hyperinsulinaemia-hyperaminoacidaemia on leg muscle protein synthesis and breakdown: reassessment of the two-pool arterio-venous balance model. J Physiol. 2015 Sep 15;593(18):4245-57. doi: 10.1113/JP270774. Epub 2015 Aug 14.
- Smith GI, Commean PK, Reeds DN, Klein S, Mittendorfer B. Effect of Protein Supplementation During Diet-Induced Weight Loss on Muscle Mass and Strength: A Randomized Controlled Study. Obesity (Silver Spring). 2018 May;26(5):854-861. doi: 10.1002/oby.22169.
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 (Faktiske)
1. januar 2012
Primær fullføring (Faktiske)
1. mars 2017
Studiet fullført (Faktiske)
1. mars 2017
Datoer for studieregistrering
Først innsendt
20. februar 2012
Først innsendt som oppfylte QC-kriteriene
20. februar 2012
Først lagt ut (Anslag)
24. februar 2012
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
27. mars 2017
Siste oppdatering sendt inn som oppfylte QC-kriteriene
22. mars 2017
Sist bekreftet
1. mars 2017
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- CRPS-201107354
- 1R01DK094483-01A1 (U.S. NIH-stipend/kontrakt)
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. .