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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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Netherlands Trial Register |
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Last refreshed on:
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28 April 2013 |
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Main ID: |
NTR825 |
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Date of registration:
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23/11/2006 |
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Primary sponsor: |
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Public title:
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Study on Cost-Effectiveness of Personality Disorder Treatment.
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Scientific title:
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A quasi-experimental prospective study of dose-effect relations in and possibilities of matched care for pscychotherapeutic treatment of personality disorders. - SCEPTRE |
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Date of first enrolment:
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1/9/2003 |
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Target sample size:
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821 |
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Recruitment status: |
complete |
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URL:
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http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=825 |
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Study type:
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intervention |
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Study design:
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Randomised: No; Masking: None; Control: Not applicable; Group: Parallel; Type: -
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Countries of recruitment
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The Netherlands
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Contacts
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Name:
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Helene
Andrea |
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Address:
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Viersprong Institute for Studies on Personality Disorders (VISPD)
P.O. Box 7
4660 AA
Halsteren
The Netherlands |
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Telephone:
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+31 (0)164 632200 |
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Email:
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helene.andrea@deviersprong.nl |
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Affiliation:
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Name:
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Roel
Verheul |
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Address:
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Viersprong Institute for Studies on Personality Disorders (VISPD)
P.O. Box 7
4660 AA
Halsteren
The Netherlands |
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Telephone:
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+31 (0)164 632200 |
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Email:
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roel.verheul@deviersprong.nl |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: 1. At least one DSM-IV axis-II diagnosis;
2. An indication for psychotherapeutic treatment aiming at structural improvement of the personality pathology (besides symptomatic and/or functional improvement).
Exclusion criteria: 1. Insufficient command of Dutch language;
2. Severe cognitive impairments;
3. Mental retardation;
4. Axis-I schizophrenia.
Age minimum:
Age maximum:
Gender:
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Health Condition(s) or Problem(s) studied
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Personality disorder
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Intervention(s)
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Psychotherapeutic treatment programs for patients with personality pathology that will be distinguished from one another according to the following dosages: 1. Short (maximum of 6 months) outpatient; 2. Short day hospital; 3. Short inpatient; 4. Long (at least 6 months) outpatient; 5. Long day hospital; 6. Long inpatient.
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Primary Outcome(s)
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1. Structural improvement of personality pathology (assessed with oq-45, sipp); 2. Quality Adjusted Life Years (QALYs).
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Secondary Outcome(s)
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1. Symptomatic improvement (assessed with the SCL-90);
2. Functional improvement (assessed with, amongst others, questions regarding work situatin and care consumption);
3. Quality of life.
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Secondary ID(s)
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ISRCTN73817429
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N/A
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Source(s) of Monetary Support
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Psychotherapeutic Center De Viersprong
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