- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT05276193
GamReg Sweden - Quality Register for Gambling and Gaming Disorders
This is a quality register for the monitoring of clinical assessment and treatment for gambling disorder and gaming disorder in Swedish health care.
This register is held by Region Skåne, the health care organization of Skåne in southern Sweden, and administered by Register center South, which is associated with health care services in the southern regions of Sweden (the establishment of quality registers in Swedish health care relies upon a national legislation). Quality registers by themselves do not represent formal research projects. However, future research projects can use quality registers, such as the present one, as a data source for future research projects in case they are approved by an ethics authority.
Clinical study variables collected in the register include the following (examples):
- gender, age, occupation, living conditions
- if applicable, types of gambling associated with the treatment needs
- if applicable, type of problematic video gaming
- type of referral to the present treatment contact
- treatment history in psychiatry, social services, enforcement agency
- history of suicidal behavior
- alcohol and drugs problems requiring assessment or treatment
- violence victimization
- type of treatment provided to the patient
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Forventet)
Kontakter og lokationer
Studiekontakt
- Navn: Anders Håkansson, PhD
- Telefonnummer: +46 46 175596
- E-mail: anders.c.hakansson@skane.se
Studiesteder
-
-
-
Malmö, Sverige
- Rekruttering
- Malmö Addiction Center
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- All patients assessed and treated at units where treatment of problem gambling or problem gaming is provided
Exclusion Criteria:
- Patients who - in a standardized opt-out procedure (following standard of national regulation for quality registers) - refuse participation in the quality register
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Observationsmodeller: Andet
- Tidsperspektiver: Fremadrettet
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Treatment uptake
Tidsramme: 1 year
|
Number of patients treated (assessed annually)
|
1 year
|
|
Characteristics of treatment-seeking patients
Tidsramme: 1 year
|
Characteristics of treatment-seeking patients (socio-demographic and mental health co-morbidities), assessed annually
|
1 year
|
|
Distribution of treatment methods provided (assessed annually)
Tidsramme: 1 year
|
Distribution of treatment methods provided (cognitive-behavioral therapy, motivational interviewing, psycho-dynamic treatment, medication, etc, assessed annually)
|
1 year
|
Samarbejdspartnere og efterforskere
Sponsor
Publikationer og nyttige links
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
- GamReg Sweden
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 .