- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg 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.
.
Studieoversigt
Status
Betingelser
Undersøgelsestype
Tilmelding (Forventet)
Kontakter og lokationer
Studiesteder
-
-
-
Drammen, Norge
- Rekruttering
- Trude G Klevan
-
Kontakt:
- Trude G Klevan
- Telefonnummer: 004735575420 004735575420
- E-mail: Trude.Goril.Klevan@usn.no
-
Kontakt:
- Marit Borg
- Telefonnummer: 004735575420 004747289487
- E-mail: marit.borg@usn.no
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
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
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
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.
|
Explore recovery orientation of mental health services in a municipality through:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Contribute to the knowledge base on what recovery orientation of services involves
Tidsramme: The aims of the study will be explored through interviews and fieldwork over an anticipated period of 2 years
|
The anticipated outcome is to obtain insight on how recovery orientation of mental health services affects roles, knowledge and collaboration in a Norwegian municipality.
|
The aims of the study will be explored through interviews and fieldwork over an anticipated period of 2 years
|
Samarbejdspartnere og efterforskere
Samarbejdspartnere
Efterforskere
- Studiestol: Heidi c Kapstad, PhD, University of South-Eastern Norway
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- UCSNorway
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .