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Undersøgelse af resultater fra diabetesforebyggelsesprogrammet (DPPOS)

Diabetes Prevention Program (DPP) var et multicenterforsøg, der undersøgte evnen af ​​en intensiv livsstil eller metformin til at forhindre eller forsinke udviklingen af ​​diabetes i en højrisikopopulation på grund af tilstedeværelsen af ​​nedsat glukosetolerance (IGT, 2 timers glukose af 140-199 mg/dl). DPP er afsluttet tidligt og demonstrerer, at livsstil reducerede diabetesdebut med 58% og metformin reducerede diabetesdebut med 31%.

DPPOS (2002-2013) er designet til at drage fordel af de videnskabeligt og klinisk værdifulde DPP-deltagere. Denne gruppe af deltagere udgør næsten 50 % minoritet og repræsenterer den største risikopopulation, der nogensinde er undersøgt. Der er stadig klinisk vigtige forskningsspørgsmål, der fokuserer på 1) holdbarheden af ​​den forudgående DPP-intervention, 2) bestemmelse af det kliniske forløb af præcist kendt nyopstået diabetes, især vedrørende mikrovaskulær sygdom, CVD-risikofaktorer og åreforkalkning, 3) nøje undersøgelse af disse emner hos mænd vs kvinder og i minoritetsbefolkninger.

Hovedformålene med DPPOS-3 (2014-2025) drager fordel af den langsigtede randomiserede eksponering af studiekohorten for metformin og ældningen af ​​DPPOS-kohorten. Metformineksponeringen og den høje grad af undersøgelsesretention og overholdelse (~85 % af DPPOS-kohorten fortsætter med at deltage i årlige og midtårsbesøg) gør det muligt for DPPOS-3 at undersøge langsigtede virkninger af metformin på hjerte-kar-sygdomme (CVD) og cancer resultater, resultater af stor klinisk interesse og betydning.

Studieoversigt

Detaljeret beskrivelse

Den aktuelle DPPOS Executive Summary og protokol samt DPPOS protokol og livsstilsmanualer og publikationer er tilgængelige på: http://www.dppos.org

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

2779

Fase

  • Fase 3

Kontakter og lokationer

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

Studiesteder

    • Maryland
      • Rockville, Maryland, Forenede Stater, 20852
        • George Washington University

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

25 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Beskrivelse

Deltagelse som frivillig i Diabetes Prevention Program (DPP).

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

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

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: 1 Original livsstil
randomiseret til unmasked Intensive Lifestyle under DPP og tilbudt Intensive Lifestyle Group Session, DPPOS Group Lifestyle plus DPPOS Boost Lifestyle sessioner i DPPOS fase 1 og 2
Kvartalsvise gruppelivsstilssessioner
Udover kvartalsgruppe, 2 ekstra klasser om året og en årlig 15 minutters kontrol.
16 sessions pensum i gruppeformat. I DPP leveret til ILS som individuelle sessioner
Andre navne:
  • Intensiv livsstilssession (ILS)
Aktiv komparator: 2 Original Metformin
randomiseret til den maskerede metforminbehandlingsgruppe under DPP og fortsat åben etiket i DPPOS. Deltagerne blev også tilbudt Intensiv Lifestyle Group Session, DPPOS Group Lifestyle i DPPOS fase 1 og 2.
Kvartalsvise gruppelivsstilssessioner
16 sessions pensum i gruppeformat. I DPP leveret til ILS som individuelle sessioner
Andre navne:
  • Intensiv livsstilssession (ILS)
Administreret som 850 mg to gange dagligt, maskeret i DPP og åben etiket i DPPOS
Andre navne:
  • Glucophage
Placebo komparator: 3 Original placebo
randomiseret til maskeret placebo under DPP og tilbudt Intensiv Lifestyle Group Session, DPPOS Group Lifestyle i DPPOS fase 1 og 2
Kvartalsvise gruppelivsstilssessioner
16 sessions pensum i gruppeformat. I DPP leveret til ILS som individuelle sessioner
Andre navne:
  • Intensiv livsstilssession (ILS)

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Forekomst af aggregeret mikrovaskulær komplikation
Tidsramme: Resultaterne blev vurderet fra 2012-2013 (ca. 2 år).
Aggregeret mikrovaskulær sygdom er defineret som den gennemsnitlige prævalens af 3 komponenter: (1) retinopati målt ved fotografering (ETDRS på 20 eller mere); (2) neuropati påvist af Semmes Weinstein 10 gram monofilament, og (3) nefropati baseret på estimeret glomerulær filtrationshastighed (eGFR ved kronisk nyresygdom (CKD-Epi) ligning) (<45 ml/min, bekræftet) og albumin-til- kreatininforhold i pleturin (> 30 mg/g, bekræftet).
Resultaterne blev vurderet fra 2012-2013 (ca. 2 år).
Number of Participants With Diabetes.
Tidsramme: Outcomes were assessed from 1996-2020 for median follow-up of 21 years and a maximum follow-up of 23 years including a median of 3 years in DPP in all participants enrolled in DPPOS.
Primary outcome defined according to American Diabetes Association criteria (fasting plasma glucose level >= 126 mg/dL [7.0 mmol/L] or 2-hour plasma glucose >= 200 mg/dL [11.1 mmol/L], after a 75 gram oral glucose tolerance test (OGTT), and confirmed with a repeat test).
Outcomes were assessed from 1996-2020 for median follow-up of 21 years and a maximum follow-up of 23 years including a median of 3 years in DPP in all participants enrolled in DPPOS.
Number of Participants With Total Cancer Except Non-melanoma Skin Cancer
Tidsramme: Outcomes were assessed from 1996-2020 (approximately 24 years).
All primary cancers except non-melanoma skin cancer that occurred after randomization in DPP
Outcomes were assessed from 1996-2020 (approximately 24 years).
Number of Participants With Major Adverse Cardiovascular Events (MACE): Myocardial Infarction (MI), Stroke, or Cardiovascular Death (CVD)
Tidsramme: Outcomes were assessed from 1996-2019 over a total median follow-up of 21 years since DPP randomization
MACE includes MI, stroke or CVD death that occurred after randomization and adjudicated by an outcomes committee who are blinded to treatment assignment.
Outcomes were assessed from 1996-2019 over a total median follow-up of 21 years since DPP randomization

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Subklinisk åreforkalkning
Tidsramme: Resultaterne blev vurderet fra 2012-2013 (ca. 2 år).
Målt ved hjælp af koronararterieforkalkning (CAC).
Resultaterne blev vurderet fra 2012-2013 (ca. 2 år).
Cognitive Function
Tidsramme: Outcomes were assessed in visit year 8 starting in 2010
Cognitive function was defined by tests of memory SEVLT (Spanish English Verbal Learning Test) and executive function, DSST (Digit Symbol Substitution Test). The measure of memory was the Spanish English Verbal Learning Test (SEVLT). The SEVLT consists of recalling a list of 15 words in three trials of immediate recall and one trial after a distractor list. The total number of correct words recalled after four trials is the outcome reported.The test of frontal-executive abilities was the total score in the Digit Symbol Substitution Test (DSST). The DSST is a test in which participants try to match numbers to symbols in 90 s. The total number of correct answers is reported.
Outcomes were assessed in visit year 8 starting in 2010
Short Physical Performance Battery
Tidsramme: Outcomes were assessed in visit years 8, 10 , and 15 which started in 2010, 2012, and 2017, respectively
Physical function is measured using the short physical performance battery (SPPB), which ranges from 0-12 and is comprised of measures of 1) time to walk 3-4 meters, 2) balance, i.e., side-by-side stand, semi-tandem stand, and tandem stand, and 3) repeated chair stands and derived as SPPB= (balance score + gait score + chair score). Each sub scale is 0, 1, 2, 3 or 4 depending on the gender specific quintiles with 0 being the lowest and 4 being the highest functional status as described in Guralnik JM, Simonsick EM, Ferrucci L, et al. A short physical performance battery assessing lower extremity function: association with self-reported disability and prediction of mortality and nursing home admission. J Gerontol. 1994 Mar 1;49(2):M85-94.
Outcomes were assessed in visit years 8, 10 , and 15 which started in 2010, 2012, and 2017, respectively
Frailty
Tidsramme: Outcomes were assessed in DPPOS Visits years 8, 10 and 15 which started in 2010, 2012, and 2017
Description: The Cardiovascular Health Study Frailty score is based on 5 frailty characteristics: slow walking speed, low energy expenditure, exhaustion, weak grip strength, and unintentional weight loss.
Outcomes were assessed in DPPOS Visits years 8, 10 and 15 which started in 2010, 2012, and 2017
Mortality
Tidsramme: Outcomes were assessed throughout follow-up from 1996 to 2019. National Death Index search conducted in 2019 using early release data as of Dec 2018.
All cause-mortality through clinic reports and National Death Index search
Outcomes were assessed throughout follow-up from 1996 to 2019. National Death Index search conducted in 2019 using early release data as of Dec 2018.

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Development of Diabetes by Sex
Tidsramme: Outcomes were assessed from 1996-2008 (approximately 12 years including 6 years of DPP).
Primary outcome defined according to American Diabetes Association criteria (fasting plasma glucose level >= 126 mg/dL [7.0 mmol/L] or 2-hour plasma glucose >= 200 mg/dL [11.1 mmol/L], after a 75 gram oral glucose tolerance test (OGTT), and confirmed with a repeat test). Stratified by sex among DPP participants who enrolled in DPPOS 2002-2008
Outcomes were assessed from 1996-2008 (approximately 12 years including 6 years of DPP).
Development of Diabetes by Race
Tidsramme: Outcomes were assessed from 1996-2008 (approximately 12 years including 6 years of DPP).
Primary outcome defined according to American Diabetes Association criteria (fasting plasma glucose level >= 126 mg/dL [7.0 mmol/L] or 2-hour plasma glucose >= 200 mg/dL [11.1 mmol/L], after a 75 gram oral glucose tolerance test (OGTT), and confirmed with a repeat test). Stratified by race among DPP participants who enrolled in DPPOS 2002-2008
Outcomes were assessed from 1996-2008 (approximately 12 years including 6 years of DPP).
Prevalence of Aggregate Microvascular Complication by Sex
Tidsramme: Outcomes were assessed from 2012-2013 (approximately 2 years).
Aggregate microvascular disease is defined as the average prevalence of 3 components: (1) retinopathy measured by photography (ETDRS of 20 or greater); (2) neuropathy detected by Semmes Weinstein 10 gram monofilament, and (3) nephropathy based on estimated glomerular filtration rate (eGFR by chronic kidney disease (CKD-Epi) equation ) (<45 ml/min, confirmed) and albumin-to-creatinine ratio in spot urine (> 30mg/gm, confirmed). General estimating equation models (GEE) were used to estimate average (marginal) prevalence accounting for correlations among the 3 components.
Outcomes were assessed from 2012-2013 (approximately 2 years).
Prevalence of Aggregate Microvascular Complication by Race
Tidsramme: Outcomes were assessed from 2012-2013 (approximately 2 years).
Aggregate microvascular disease is defined as the average prevalence of 3 components: (1) retinopathy measured by photography (ETDRS of 20 or greater); (2) neuropathy detected by Semmes Weinstein 10 gram monofilament, and (3) nephropathy based on estimated glomerular filtration rate (eGFR by chronic kidney disease (CKD-Epi) equation ) (<45 ml/min, confirmed) and albumin-to-creatinine ratio in spot urine (> 30mg/gm, confirmed). General estimating equation models (GEE) were used to estimate average (marginal) prevalence accounting for correlations among the 3 components.
Outcomes were assessed from 2012-2013 (approximately 2 years).
Number of Participants With Total Cancer Except Non-melanoma Skin Cancer by Sex
Tidsramme: Outcomes were assessed from 1996-2020 (approximately 24 years).
All primary cancers except non-melanoma skin cancer that occurred after randomization in DPP
Outcomes were assessed from 1996-2020 (approximately 24 years).
Number of Participants With Total Cancer Except Non-melanoma Skin Cancer by Race
Tidsramme: Outcomes were assessed from 1996-2020 (approximately 24 years).
All primary cancers except non-melanoma skin cancer that occurred after randomization in DPP
Outcomes were assessed from 1996-2020 (approximately 24 years).
Number of Participants With Major Adverse Cardiovascular Events (MACE): Myocardial Infarction (MI), Stroke, or Cardiovascular Death (CVD) By Sex
Tidsramme: Outcomes were assessed from 1996-2019 over a total median follow-up of 21 years since DPP randomization
MACE includes MI, stroke or CVD death that occurred after randomization and adjudicated by an outcomes committee who are blinded to treatment assignment stratified by sex
Outcomes were assessed from 1996-2019 over a total median follow-up of 21 years since DPP randomization
Number of Participants With Major Adverse Cardiovascular Events (MACE): Myocardial Infarction (MI), Stroke, or Cardiovascular Death (CVD) By Race
Tidsramme: Outcomes were assessed from 1996-2019 over a total median follow-up of 21 years since DPP randomization
MACE includes MI, stroke or CVD death that occurred after randomization and adjudicated by an outcomes committee who are blinded to treatment assignment.
Outcomes were assessed from 1996-2019 over a total median follow-up of 21 years since DPP randomization

Samarbejdspartnere og efterforskere

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

Efterforskere

  • Studiestol: David M. Nathan, MD, Massachusetts General Hospital
  • Ledende efterforsker: Marinella Temprosa, PhD, George Washington University Biostatistics Center
  • Studieleder: Barbara Linder, MD, PhD, NIDDK Project Scientist
  • Ledende efterforsker: Kathleen Jablonski, PhD, George Washington University Biostatistics Center
  • Ledende efterforsker: Ronald B Goldberg, MD, University of Miami
  • Ledende efterforsker: Helen P Hazuda, MD, The University of Texas Health Science Center at San Antonio
  • Ledende efterforsker: Dana Dabelea, MD, PhD, University of Colorado, Denver
  • Ledende efterforsker: Medha Munshi, MD, Joslin Diabetes Center
  • Ledende efterforsker: Steven Kahn, MB, ChB, University of Washington
  • Ledende efterforsker: Happy Araneta, PhD,MPH, University of California, San Diego
  • Ledende efterforsker: Karol E Watson, MD, University of California, Los Angeles
  • Ledende efterforsker: Angela Brown, MD, Washington University School of Medicine
  • Ledende efterforsker: Sherita Hill Golden, MD, MHS, Johns Hopkins School of Medicine
  • Ledende efterforsker: David S Schade, MD, The University of New Mexico
  • Ledende efterforsker: Elizabeth Venditti, PhD, University of Pittsburgh
  • Ledende efterforsker: Marjerie Mau, MD, University of Hawaii
  • Studieleder: Christine Lee, MD, NIDDK Project Scientist
  • Ledende efterforsker: Sunder Mudaliar, MD, University of California, San Diego
  • Ledende efterforsker: Amisha Wallia, MD, Northwestern University
  • Ledende efterforsker: Jill Crandall, MD, Albert Einstein College of Medicine
  • Ledende efterforsker: Celeste Thomas, MD, University of Chicago
  • Ledende efterforsker: Owen Carmichael, PhD, Pennington Biomedical Research Center
  • Ledende efterforsker: Intekhab Ahmed, MD, Jefferson Medical College of Thomas Jefferson University
  • Ledende efterforsker: Samuel Dagogo-Jack, MD, MB, University of Tennessee
  • Ledende efterforsker: Blandine Laferrere, MD, Columbia University
  • Ledende efterforsker: Mary de Groot, PhD, Indiana University
  • Ledende efterforsker: Saurabh Sharma, MD, Medstar Health Research Institute
  • Ledende efterforsker: Robert Hanson, MD, SW Indian Center - Phoenix
  • Ledende efterforsker: Linda Delahanty, MD, Massachusetts General Hospital
  • Ledende efterforsker: Vallabh Shah, PhD, SW Indian Center - Zuni/Shiprock

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)

31. juli 1996

Primær færdiggørelse (Faktiske)

28. februar 2020

Studieafslutning (Faktiske)

30. april 2022

Datoer for studieregistrering

Først indsendt

4. juni 2002

Først indsendt, der opfyldte QC-kriterier

4. juni 2002

Først opslået (Anslået)

5. juni 2002

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

30. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

27. juli 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-planbeskrivelse

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Repository

IPD-delingstidsramme

2002-2025

IPD-delingsadgangskriterier

Instruktioner for adgang er detaljeret her: https://repository.niddk.nih.gov/pages/overall_instructions/

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ja

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

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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