- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04138459
Recovery - a Collaborative Project
Development of Recovery Oriented Practices, Knowledge and Collaboration in a Norwegian Municipality. An Explorative Study
In Norway, official guidelines and policies state that recovery oriented services in the field of mental health and substance abuse services is a desirable goal.
This collaborative research project aims to provide in-depth knowledge of how recovery oriented practices and collaboration in the mental health and substance abuse services in the municipality of New Drammen develop over a three-year period.
Using qualitative methods, the main aim of the study is to explore what recovery orientation of services in mental health and substance abuse presupposes and involves related to roles, collaboration and knowledge.
To explore these issues, service users will be interviewed together with their primary mental health professional.
The study will also apply observational fieldwork in order to observe recovery oriented practices between service users and professionals and between professionals.
An advisory group consisting of people with background as service users, mental health clinicians and service leaders will contribute throughout the project.
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Study Overview
Status
Conditions
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Trude G Klevan, PhD
- Phone Number: 004735575420 004735575420
- Email: Trude.Goril.Klevan@usn.no
Study Contact Backup
- Name: Marit c Borg, PhD
- Phone Number: 0047481995 004747289487
- Email: marit.borg@usn.no
Study Locations
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Drammen, Norway
- Recruiting
- Trude G Klevan
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Contact:
- Trude G Klevan
- Phone Number: 004735575420 004735575420
- Email: Trude.Goril.Klevan@usn.no
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Contact:
- Marit Borg
- Phone Number: 004735575420 004747289487
- Email: marit.borg@usn.no
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Adults who have received community mental health and / or substance abuse services for the past year or longer, due to moderate or severe mental health and / or substance abuse problems.
Inclusion Criteria:
- receives community mental health services due to mental health and /or substance abuse related problems
- Above 18 years old
Exclusion Criteria:
- Under the age of 18
- Mental health workers in the municipality, working in mental health and substance abuse services
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Qualitative exploration
Ten community mental health service users will be interviewed with their most important mental health worker to explore how recovery orientation of services affects roles and collaboration.
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Explore recovery orientation of mental health services in a municipality through:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Contribute to the knowledge base on what recovery orientation of services involves
Time Frame: The aims of the study will be explored through interviews and fieldwork over an anticipated period of 2 years
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The anticipated outcome is to obtain insight on how recovery orientation of mental health services affects roles, knowledge and collaboration in a Norwegian municipality.
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The aims of the study will be explored through interviews and fieldwork over an anticipated period of 2 years
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Collaborators and Investigators
Collaborators
Investigators
- Study Chair: Heidi c Kapstad, PhD, University of South-Eastern Norway
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UCSNorway
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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