Attitudes Towards Buprenorphine and Methadone
Att-1
Attitudes of Patients With Opioid-Substitution and Their Therapists Towards and Buprenorphine and Methadone
1 other identifier
observational
180
1 country
1
Brief Summary
Main intention of this study is to find out whether there is a difference between the attitudes towards opioid- substitution of opioid dependent patients under substitution with methadone, buprenorphine or without substitution and their therapists
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started May 2009
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2009
CompletedFirst Submitted
Initial submission to the registry
May 28, 2009
CompletedFirst Posted
Study publicly available on registry
June 2, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2010
CompletedJune 2, 2009
May 1, 2009
4 months
May 28, 2009
May 28, 2009
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Attitude toward buprenorphine compared over the four groups
one time of measurement
Secondary Outcomes (1)
Treatment success; Treatment conditions; Consumption of substances
one point of measurement
Study Arms (4)
Buprenorphine
opioid-dependent patients with buprenorphine substitution
methadone
opioid-dependent patients substituted with methadone
no substitution
opioid-dependent patients without substitution
therapists
therapists of the patients
Interventions
interview using questionnaires
Eligibility Criteria
Patients of therapeutic communities, in- and out-patients and their therapists
You may qualify if:
- Age between 18 and 65 years
- Opioid-dependent with substitution with buprenorphine,
- methadone or without substitution
- Sufficient knowledge of German language
You may not qualify if:
- Inability to give informed consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Psychiatric University Hospital
Zurich, Canton of Zurich, 8032, Switzerland
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Lukas Boesch, PhD
Psychiatric University Hospital, Zurich
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
May 28, 2009
First Posted
June 2, 2009
Study Start
May 1, 2009
Primary Completion
September 1, 2009
Study Completion
June 1, 2010
Last Updated
June 2, 2009
Record last verified: 2009-05