- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01538836
Calorie Restriction, Protein Supplementation and Metabolic Health (CRPS)
22 mars 2017 uppdaterad 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.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Faktisk)
75
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Missouri
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Saint Louis, Missouri, Förenta staterna, 63110
- Washington University School of Medicine
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
50 år till 65 år (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Ja
Kön som är behöriga för studier
Kvinna
Beskrivning
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
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
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Aktiv komparator: Viktminskning med normalt proteinintag
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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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Inget ingripande: Weight maintenance
Weight maintenance with normal protein intake
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Experimentell: 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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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Change in muscle volume
Tidsram: 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
Tidsram: 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
Tidsram: 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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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Förändring i bakteriepopulationer som finns i avföringen
Tidsram: Baslinje och vid 10 % viktminskning i kalorirestriktionsgrupper och ~6 till 7 månader i viktupprätthållande gruppen
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Baslinje och vid 10 % viktminskning i kalorirestriktionsgrupper och ~6 till 7 månader i viktupprätthållande gruppen
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Change in insulin sensitivity
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Allmänna publikationer
- 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.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
1 januari 2012
Primärt slutförande (Faktisk)
1 mars 2017
Avslutad studie (Faktisk)
1 mars 2017
Studieregistreringsdatum
Först inskickad
20 februari 2012
Först inskickad som uppfyllde QC-kriterierna
20 februari 2012
Första postat (Uppskatta)
24 februari 2012
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
27 mars 2017
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
22 mars 2017
Senast verifierad
1 mars 2017
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- CRPS-201107354
- 1R01DK094483-01A1 (U.S.S. NIH-anslag/kontrakt)
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .
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