- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00239122
Recovery Therapy Trial
October 12, 2005 updated by: Melbourne Health
Applicability of CBT to Unselected Mental Health Service Clients With Psychotic Disorders
This project will systematically apply a specialist version of Cognitive Behaviour Therapy (CBT), known as Recovery Therapy, to a random sample of patients with psychotic disorders.
Previously, the therapy has been developed and efficacy established, but the extent of applicability to (unselected) mental health service patients is unknown.
The main aim is to establish the extent to which this therapy is acceptable and effective for mental health service clients.
A secondary aim is to develop guidelines for the conduct of such therapy in public mental health settings.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment
94
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Victoria
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Epping, Victoria, Australia, 3076
- Whittlesea Community Mental Health Service
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Preston, Victoria, Australia, 3072
- Darebin Community Mental Health Service
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years to 65 years (ADULT, OLDER_ADULT, CHILD)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- acceptance by the participating Community Mental Health Services for case management
- a preliminary DSM-IV diagnosis of schizophrenia, schizoaffective disorder, mood disorder with psychotic features, or delusional disorder
- a recovery "need" in one of the areas addressed by the therapy
Exclusion Criteria:
- a preliminary DSM-IV diagnosis of brief psychotic disorder, drug-induced psychosis, mood disorder without hallucinations or delusions, or any other disorder (eg. personality disorder, PTSD) even where psychotic features are/have been present
- non-English speaking
- comorbid intellectual disability
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: SINGLE_GROUP
- Masking: NONE
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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To determine the applicability of cognitive behaviour therapy for psychosis in the "real world" setting of ordinary mental health services
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Secondary Outcome Measures
Outcome Measure |
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To establish rates of uptake of Recovery Therapy amongst clients at a community mental health service
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To establish effectiveness of therapy in clients who received a defined length of therapeutic contact (12-24 sessions)
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To identify factors predicting uptake and effectiveness
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: John Farhall, BA(Hons), MA, LaTrobe University, NorthWestern Mental Health
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2000
Study Completion
February 1, 2004
Study Registration Dates
First Submitted
October 12, 2005
First Submitted That Met QC Criteria
October 12, 2005
First Posted (ESTIMATE)
October 14, 2005
Study Record Updates
Last Update Posted (ESTIMATE)
October 14, 2005
Last Update Submitted That Met QC Criteria
October 12, 2005
Last Verified
October 1, 2005
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E00013
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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