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Tracking Service Use and Outcomes II:First Episode Psychosis and Psychotic Disorders Clinic

12. september 2006 opdateret af: Hamilton Health Sciences Corporation

Main Research questions:

  1. Who are the patients referred for treatment at the Psychotic Disorders Clinic?
  2. What are the outcomes from treatment for first episode psychosis in multiple outcome domains?
  3. What hospital resources are used over the early course of the illness?
  4. How satisfied are patients and family with the treatment and services they received? This is an important study that will help us evaluate the service and treatment offered by the Psychotic Disorders Clinic's specialized early intervention program,which helps young people experiencing early stages of psychotic illness.A growing body of evidence suggests that intervening earlier in the course of the illness with specialized and complimentary pharmacological and psychosocial treatment may be associated with improved outcomes.

Studieoversigt

Status

Afsluttet

Betingelser

Detaljeret beskrivelse

The project is primarily a descriptive study of individuals experiencing their first episode of psychosis presenting at the Psychotic Disorders Clinic/Early Intervention Program.

The objectives of the study are:

  1. Track multi-dimensional outcomes within the program
  2. Track service use
  3. Compare outcomes for this early intervention program with outcomes noted in published follow up studies
  4. Evaluate effectiveness of the Psychotic Disorders Clinic in improving outcomes for persons experiencing their first episode of psychosis

Undersøgelsestype

Observationel

Kontakter og lokationer

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

Studiesteder

  • Canada
    • Ontario
      • Hamilton, Ontario, Canada, L8N 1Y2
        • Cleghorn Program-Early Intervention in Psychosis.St Joseph's Healthcare Hamilton/Hamilton Health Sciences

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

16 år til 50 år (Barn, Voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • male or female between ages of 16 to 50 years of age
  • capable of providing informed consent
  • receiving treatment voluntarily
  • experiencing a "first episode of psychosis" defined as the first episode of illness and where the subject,at presentation,meets DSM-IV criteria for one of the following diagnoses:schizophrenia,schizophreniform disorder,schizoaffective disorder,brief psychotic disorder,delusional disorder,and psychosis NOS

Exclusion Criteria:

  • primary diagnosis of mood disorder
  • diagnosis of substance-induced psychosis
  • diagnosis of psychosis due to a general medical condition
  • diagnosis of mental retardation
  • diagnosis of developmental disorder
  • has received antipsychotic treatment for greater than 1 month
  • has received treatment for an earlier episode of psychosis from which there has been a remission of symptoms for greater than 3 months

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Observationsmodeller: Defineret befolkning
  • Tidsperspektiver: Fremadrettet

Samarbejdspartnere og efterforskere

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

Sponsor

Hamilton Health Sciences Corporation

Efterforskere

  • Ledende efterforsker: Suzanne Archie, MD,FRCP(C), Assistant Professor Dept of Psychiatry and Behavioural Neurosciences McMaster University.Active Medical Staff Hamilton Health Sciences.Clinical Director of Cleghorn Early Intervention in Psychosis Program and Psychotic Disorders Clinic

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

1. januar 2004

Datoer for studieregistrering

Først indsendt

1. november 2005

Først indsendt, der opfyldte QC-kriterier

1. november 2005

Først opslået (Skøn)

3. november 2005

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

13. september 2006

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

12. september 2006

Sidst verificeret

1. september 2006

Mere information

Begreber relateret til denne undersøgelse

Nøgleord

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • REB #04-203

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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