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Multicenter Research Study to Build a Repository to Study Chronic Diseases in Indiana (IHS)

5 september 2013 bijgewerkt door: Fairbanks Institute

Multicenter Research Study to Build a Repository That Will Allow Researchers to Study Chronic Diseases in the Population of Central Indiana

Blood samples and health information (e.g., age at diagnosis, test results) are collected for the purposes of genetic research. The blood samples are assigned a number and stored in a repository for safe keeping until they are needed for a research project. Participants are persons who are healthy (not having high blood pressure, diabetes, or high cholesterol levels) or persons who have Diabetes Mellitus Type II(T2D) and live in Indiana. Participants complete a questionnaire at the time the blood sample is drawn. Visits are repeated at 2 and 5 years after initial contact. Researchers apply to the Fairbanks Institute for use of the blood samples and health information minus participant names and contact information. Their research is required to be related to find genes or substances made by genes that may be involved in Diabetes Mellitus Type II with the purpose of improving the investigators understanding of the illness potentially leading to the development of new diagnostic tools for identifying the illness, new treatments,or preventative measures.

Studie Overzicht

Toestand

Actief, niet wervend

Conditie

Diabetes mellitus type II

Gedetailleerde beschrijving

Study Aim:

The purpose of this study is to create an extensively annotated bio-repository platform for hypothesis-driven research that will lead to advancements in the diagnosis, treatment and prevention of diseases common to the population of Indiana. The second phase of this research platform will be created by collecting blood samples from two groups of individuals in the Central Indiana community, one with documented evidence of Diabetes Mellitus Type II(T2D), and a second group of age, gender and ethnicity matched individuals without clinical evidence of Diabetes. Each individual's blood sample will be linked to their clinical, demographic and epidemiological information, gathered both retrospectively and prospectively.

Recruitment:

This study will include 500 individuals with T2D (the T2D Group) and 500 individuals who are age, gender, and ethnicity matched to the T2D Group, but without presentation of clinical evidence of T2D (the Control Group). To reflect the growing representation of Hispanics in Central Indiana, Hispanics will be overly recruited in both groups so that the study population accurately reflects the general population of Central Indiana.

Follow-up:

As this is a prospective, longitudinal study, follow-up of study subjects is intended to include two follow up visit and continue indefinitely, unless, of course, at any time, consent for further follow-up is withdrawn by the subject. Follow-up will include visits at 2 and 5 years post initial contact and continuing access to the subject's medical record to pursue data concerning changes in the subject's health. Subjects may be contacted by telephone, mail or email every twelve months to ask if they wish to continue participation in the study. The 2 and 5 year follow up visits mirror the initial visit.

The collected dataset (made up of the collected blood samples linked to clinical and epidemiological information collected retrospectively and prospectively), will be used in medical research to find genes, or gene products such as RNA or proteins that will help in understanding the causes of disease and will guide the development of new treatments

Studietype

Observationeel

Inschrijving (Verwacht)

1000

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

Verenigde Staten
- Indiana
  - Avon, Indiana, Verenigde Staten
    - American Health Network
  - Brownsburg, Indiana, Verenigde Staten
    - Investigator's Research Group
  - Franklin, Indiana, Verenigde Staten
    - American Health Network
  - Greenfield, Indiana, Verenigde Staten
    - American Health Network
  - Indianapolis, Indiana, Verenigde Staten
    - American Health Network
  - Indianapolis, Indiana, Verenigde Staten
    - Krannert Cardiology
  - Indianapolis, Indiana, Verenigde Staten
    - Oral Health Research Institute
  - Indianapolis (Downtown), Indiana, Verenigde Staten
    - IU School of Medicine/CTSI
  - Indianapolis (Spanish speaking), Indiana, Verenigde Staten
    - Alivio Medical Center
  - Indianapolis (Spanish/English speaking), Indiana, Verenigde Staten
    - IU Medical Group
  - Muncie, Indiana, Verenigde Staten
    - American Health Network

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Geslachten die in aanmerking komen voor studie

Allemaal

Bemonsteringsmethode

Kanssteekproef

Studie Bevolking

People living in the state of Indiana

Beschrijving

Inclusion Criteria:T2D Group

Study subjects will be recruited for the T2D group based on a history confirmed by the medical record of at least one of the following:

A fasting blood glucose of greater than or equal to 126 mg/dL on two separate occasions
A random (non-fasting) blood glucose of greater than or equal to 200 mg/dL on two separate occasions
A blood glucose of greater than 200 mg/dL at 2 hours during a standard oral glucose tolerance test
A HgbA1c of greater than or equal to 6.5%

Females who are pregnant will be excluded.

Control Group

Study subjects for the Control Group will have:

no confirmed history of T2D as defined above
A fasting blood glucose of 100 mg/dL or less

Medical records will be obtained to ensure subjects meet study inclusion criteria.

Exclusion Criteria:Exclusion criteria for both the T2D Group and the Control Group are a known or reported history of:

Hepatitis B
Hepatitis C
AIDS (HIV positive)
Tuberculosis
Cancer (including melanoma, but excluding low-malignancy skin cancer)
Non-autologous bone marrow transplant
Blood transfusion within 120 days

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

Aantal groepen / cohorten

Cohorten en interventies

Groep / Cohort
People with Diabetes Mellitus Type II 500 subjects will have T2D
Healthy 500 persons who do not have T2D, hypertension or hypercholesterol

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Sponsor

Fairbanks Institute

Medewerkers

Regenstrief Institute, Inc.

Indiana University School of Medicine

Richard M. Fairbanks Foundation

BioCrossroads

Onderzoekers

Hoofdonderzoeker: Anantha Shekhar, MD, Indiana University School of Medine/CTSI

Publicaties en nuttige links

De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.

Nuttige links

Accelerated Clinical and Translational Research

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 december 2009

Primaire voltooiing (Verwacht)

1 december 2049

Studie voltooiing (Verwacht)

1 juni 2050

Studieregistratiedata

Eerst ingediend

30 juni 2011

Eerst ingediend dat voldeed aan de QC-criteria