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CSP #572 - Genetics of Functional Disability in Schizophrenia and Bipolar Illness

15. april 2015 oppdatert av: US Department of Veterans Affairs
The purpose of this study is to detect genetic associations for the development of schizophrenia (SZ) and bipolar illness (BP) by comparing Veterans with these diseases to "psychiatrically healthy" Veterans from Veterans Health Administration medical centers. In addition, the genetic basis for functional capacity and disability in Veterans affected with SZ and BP will be assessed, as will genetic predictors of suicidality and tardive dyskinesia. Finally, we will also establish a repository which allows for future genomic studies related to SZ, BP, and related disorders or sequelae.

Studieoversikt

Status

Fullført

Detaljert beskrivelse

We propose to identify the genetic basis of Veterans developing either of two major psychiatric (or "mental health") diseases: schizophrenia and bipolar disorder. The study will also examine the genetic basis of disability in everyday functions (such as employment, independent living, and self care) among the same patients. By "genetic basis," we mean how a person's genes might be a risk for developing these illnesses or being affected by them. We will compare information gathered from Veterans with these illnesses to "psychiatrically healthy" Veterans. Participants will be recruited from multiple Veterans Health Administration medical centers; the analysis of blood samples will be done in designated and approved laboratories.

Both schizophrenia and bipolar disorder are chronic psychiatric diseases associated with considerable lifelong disability; in particular, these illnesses are common in Veterans served by the Veterans Health Administration. Both of these conditions are also known to be caused in part by genes or so-called heredity; studies of the entire set of human genes (referred to as the genome) can be a tool to identify specific reasons why certain people develop certain conditions. In addition, patients with schizophrenia or bipolar disorder often have difficulty functioning in the real-world-including problems in attention and memory, or the ability to perform tasks of everyday living or have normal emotional experiences-and these "functional impairments" may also be inherited genetically. The current study is designed to help identify who is at higher risk for these diseases and related problems, so that better methods to diagnose and treat the conditions can be developed in the future.

Among other aspects of schizophrenia and bipolar disorder, suicide stands out as a very important issue to Veterans, their families, and the Veterans Health Administration. Suicide attempts and completed suicides are more common in Veterans with schizophrenia and bipolar illness (compared to Veterans without these illnesses), and this tendency may be inherited as well. Part of this study will involve determining whether specific genes might be associated with suicidal behavior. Similarly, the study will look at the genetic basis of side effects related to taking medications for these diseases.

For this research, participants will be recruited from VA sites that have extensive experience in conducting projects involving psychiatric disorders. We will collect information about the genes of these Veterans from a blood sample, and we will ask questions about health and related factors. We will also establish a repository which allows for future genomic studies related to SZ, BP, and related disorders or sequelae. The total study duration is indefinite in the setting of creating a SZ and BP repository, although the required time period for addressing the primary aims is 3.5 years. Data for a comparison ("reference") group of Veterans with medical, but not psychiatric, illnesses, will be obtained from a research initiative entitled the "VA Million Veteran Program" (VA-MVP).

Ultimately, this study attempts to advance the state-of-the-art regarding our understanding and treatment for two common mental health disorders affecting Veterans and will also serve as part of a major initiative to support "personalized" healthcare. It represents a major effort to link specific genes to illnesses, and eventually to treatments intended to relieve suffering.

Studietype

Observasjonsmessig

Registrering (Faktiske)

9356

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Alabama
      • Birmingham, Alabama, Forente stater, 35233
        • VA Medical Center, Birmingham, AL
      • Tuscaloosa, Alabama, Forente stater, 35404
        • VA Medical Center, Tuscaloosa, AL
    • Arkansas
      • No. Little Rock, Arkansas, Forente stater, 72114-1706
        • Central Arkansas VHS Eugene J. Towbin Healthcare Center, Little Rock, AR
    • California
      • Long Beach, California, Forente stater, 90822
        • VA Long Beach Healthcare System, Long Beach, CA
      • Palo Alto, California, Forente stater, 94304-1290
        • VA Palo Alto Health Care System, Palo Alto, CA
      • San Diego, California, Forente stater, 92161
        • VA San Diego Healthcare System, San Diego, CA
    • Connecticut
      • West Haven, Connecticut, Forente stater, 06516
        • VA Connecticut Healthcare System West Haven Campus, West Haven, CT
    • District of Columbia
      • Washington, District of Columbia, Forente stater, 20422
        • Washington DC VA Medical Center, Washington, DC
    • Florida
      • Miami, Florida, Forente stater, 33125
        • Miami VA Healthcare System, Miami, FL
    • Georgia
      • Decatur, Georgia, Forente stater, 30033
        • Atlanta VA Medical and Rehab Center, Decatur, GA
    • Indiana
      • Indianapolis, Indiana, Forente stater, 46202-2884
        • Richard L. Roudebush VA Medical Center, Indianapolis, IN
    • Maryland
      • Baltimore, Maryland, Forente stater, 21201
        • Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD
    • Massachusetts
      • Brockton, Massachusetts, Forente stater, 02301
        • VA Boston Healthcare System Brockton Campus, Brockton, MA
      • Leeds, Massachusetts, Forente stater, 01053-9764
        • VA Central Western Massachusetts Healthcare System, Leeds, MA
    • Minnesota
      • Minneapolis, Minnesota, Forente stater, 55417
        • Minneapolis VA Health Care System, Minneapolis, MN
    • New Mexico
      • Albuquerque, New Mexico, Forente stater, 87108-5153
        • New Mexico VA Health Care System, Albuquerque, NM
    • New York
      • New York, New York, Forente stater, 10010
        • Manhattan Campus of the VA NY Harbor Healthcare System, New York, NY
    • North Carolina
      • Salisbury, North Carolina, Forente stater, 28144
        • Salisbury W.G. (Bill) Hefner VA Medical Center, Salisbury, NC
    • Ohio
      • Cincinnati, Ohio, Forente stater, 45220
        • Cincinnati VA Medical Center, Cincinnati, OH
    • Pennsylvania
      • Philadelphia, Pennsylvania, Forente stater, 19104
        • Philadelphia VA Medical Center, Philadelphia, PA
      • Pittsburgh, Pennsylvania, Forente stater, 15240
        • VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA
    • South Carolina
      • Charleston, South Carolina, Forente stater, 29401-5799
        • Ralph H. Johnson VA Medical Center, Charleston, SC
    • Texas
      • Houston, Texas, Forente stater, 77030
        • Michael E. DeBakey VA Medical Center, Houston, TX
      • Waco, Texas, Forente stater, 76711
        • Central Texas Veterans Health Care System Waco VA Medical Center, Waco, TX
    • Washington
      • Tacoma, Washington, Forente stater, 98493
        • VA Puget Sound Health Care System American Lake Division, Tacoma, WA

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

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

Case participants: Enrolled Veterans with a confirmed diagnosis of SZ and BP.

Control participants: Psychiatrically healthy Veterans enrolled in VA Million Veteran Program.

Beskrivelse

Inclusion Criteria:

Case participants:

  • All participants must be 18 years of age or older
  • SZ patients must meet lifetime (DSM-IV) criteria for schizophrenia, any subtype
  • BP patients must have a confirmed bipolar type I diagnosis, which requires a history of a mixed or manic episode at some prior point, regardless of subsequent affective episodes
  • all patients must have medical records available in the VA CPRS
  • all patients must be competent to provide informed consent for the research

Control participants:

  • Enrollment in the VA Million Veteran Program

Exclusion Criteria:

Case participants:

  • SZ and BP patients that have participated in a previous GWAS study or are currently participating in a clinical treatment study
  • patients with physical, sensory, or intellectual limitations that preclude their assessment with performance-based measures
  • patients with active illicit drug use that might hamper assessments. Potential participants who present under the apparent influence of alcohol or drugs will be rescheduled once and excluded if they are intoxicated at their next appointment; patients identified via electronic medical record review will be screened for evidence of active drug abuse and excluded

Control participants:

  • a personal history identifiable in the VA EMR of a major psychiatric disorder related to psychosis or a first degree family member with either schizophrenia or bipolar disorder
  • major neurologic illnesses, or systemic medical illnesses, that could interfere with central nervous system function
  • current treatment with psychotropic medications aimed at psychosis, bipolar disorder, or major depression
  • anyone participating in an ongoing randomized trial of therapy for SZ or BP

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Gruppe 1

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Phenotypic cognitive and functional outcomes associated with SZ and BP
Tidsramme: 3 years
3 years

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Studiestol: Philip D. Harvey, PhD, Miami VA Healthcare System, Miami, FL

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

1. februar 2011

Primær fullføring (Faktiske)

1. juni 2014

Studiet fullført (Faktiske)

1. juli 2014

Datoer for studieregistrering

Først innsendt

21. juni 2010

Først innsendt som oppfylte QC-kriteriene

21. juni 2010

Først lagt ut (Anslag)

23. juni 2010

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

16. april 2015

Siste oppdatering sendt inn som oppfylte QC-kriteriene

15. april 2015

Sist bekreftet

1. april 2015

Mer informasjon

Begreper knyttet til denne studien

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. .

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