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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00914238
Other study ID # Danish OPUS II trial
Secondary ID
Status Completed
Phase N/A
First received May 28, 2009
Last updated October 24, 2016
Start date July 2009
Est. completion date October 2016

Study information

Verified date October 2016
Source University of Copenhagen
Contact n/a
Is FDA regulated No
Health authority Denmark: Ministry of HealthDenmark: Danish Dataprotection Agency
Study type Interventional

Clinical Trial Summary

In a randomized clinical trial, the researchers want to investigate if the positive short-term outcomes (first 1-2 years), achieved with specialized assertive intervention programme (OPUS), can be maintained for five years if the specialized treatment is sustained over the first five years in comparison to only two years of specialized treatment followed by three years of standard treatment.


Description:

The Danish OPUS I trial succeeded in randomizing 547 patients with first-episode psychosis to a two-year specialized intensive treatment program (OPUS) or standard treatment. The results clearly favored OPUS treatment, and psychotic and negative symptoms, substance abuse, adherence to treatment, use of anti-psychotic medication, user satisfaction, and use of bed days were better in OPUS compared to standard treatment. However, the five-year follow-up, three years after patients from OPUS were transferred to standard treatment, showed that the positive clinical effects were not sustained, when the intensive treatment was terminated, except from OPUS-patients being less likely to stay in institutions than patients who received standard care.

Objective: The aim in OPUS II trial is to compare the effect of five-years versus two-years specialized assertive intervention program (OPUS-treatment) for first episode psychosis on clinical symptoms, substance abuse, institutionalization, and labor market affiliation.

Hypothesis: It is possible to maintain the positive results of the intensive two-year intervention in another three years for those who keep receiving the specialized assertive intervention program.

Design: Open label randomized clinical trial. Setting: Psychiatric Center Bispebjerg and Center for Psychiatric Research Aarhus, Denmark.Participants: 400 patients with first episode of schizophrenia spectrum disorder received treatment in one of the six OPUS - teams for 1½ years.

Intervention: Another 3½ years OPUS-treatment versus ½ year OPUS-treatment and thereafter referral to standard treatment. The extended OPUS treatment consist modified assertive case management, rational pharmacotherapy, family psycho-educational intervention, group interventions to aid with recovery, social skills training, cognitive behavior therapy when indicated, and crisis intervention. OPUS-treatment is tailored to meet the individual patient's needs.


Recruitment information / eligibility

Status Completed
Enrollment 400
Est. completion date October 2016
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 37 Years
Eligibility Inclusion Criteria:

- patients aged 18 - 37 years

- first episode psychosis in schizophrenia spectrum

- treated for 1½ year in the five OPUS teams in the Capital Region and the OPUS teams in Region Midt

- patients who will give signed informed consent to participate in the trial

Exclusion Criteria:

- patients who are not treated in one of the OPUS team in the Capital Region and Region Midt

- patients who don't give signed informed consent to participate in the study

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
2 years OPUS treatment
2 years OPUS and transfer to standard treatment.
OPUS 5 years


Locations

Country Name City State
Denmark Psychiatric Center Bispebjerg Copenhagen
Denmark Psychiatric Centre Bispebjerg Copenhagen

Sponsors (5)

Lead Sponsor Collaborator
University of Copenhagen Aarhus University Hospital, Medical Research Council, Mental Health Centre Copenhagen, Region Capital Denmark

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Negative symptoms, measured with Schedule for Assessment of Negative Symptoms in Schizophrenia, (SANS) 3 years Yes
Secondary Psychotic symptoms 3 years Yes
Secondary Simultaneous remission of both psychotic and negative symptoms. 3 years Yes
Secondary Substance abuse. 3 years Yes
Secondary Suicidal behaviour. 3 years Yes
Secondary Use of bed days. 3 years Yes
Secondary Independent living. 3 Years Yes
Secondary Labour market affiliation. 3 years Yes
Secondary User satisfaction. 3 years Yes
Secondary Adherence to treatment. 3 years Yes
Secondary Compliance with medication 3 years Yes
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