The Canadian Depression Research and Intervention Network (CDRIN) Maritimes Registry
A legfontosabb adatok
- Ki végzi
- Nova Scotia Health Authority
- Hol
- Halifax (Kanada)A helyszín megnézése
- Azonosító
- Állapot
- Toboroz
- Résztvevők
- 30 000 fő, tervezett
- Kezdés
- 2015. máj.
- Várható befejezés
- 2029. dec. 31.
- A vizsgálat típusa
- Megfigyeléses
- A regiszteradat frissítve
- 2025. május 14.
Ki vehet részt
MI-összefoglaló
A vizsgálat saját részvételi feltételeiből. Gép olvasta ki az oldalon álló regiszterszövegből, ezért tévedhet. Hogy ki vehet részt, azt a lenti regiszterszöveg és a vizsgálat csapata dönti el.
A regiszter olyan, Kanada tengerparti tartományaiban élő embereket keres, akik mentális egészségügyi problémákkal (például depresszióval) kérnek vagy kapnak segítséget.
- Nem
- Férfiak és nők is részt vehetnek.
- A betegség stádiuma
- Konkrét diagnózis nem szükséges. A toborzás a depresszióval és más mentális betegségekkel élőkre irányul.
A részvétel fő kizáró okai
- Aki nem tud tájékozott beleegyezést adni, és nincs olyan helyettes döntéshozója, aki a nevében megadhatná
- Aki nem beszél angolul vagy franciául
A regiszter feltételei, szó szerint
Mind a 8 feltétel megnézéseKevesebb
Ki vehet részt
- male or female
- seeking or receiving help for mental health related problems in the maritime provinces of Canada
- able to provide informed consent or have an appropriate substitute decision maker that can provide consent on their behalf
- English or French speaking
Ki nem vehet részt
- Whilst the recruitment will be targeted to include individuals suffering with depression and other types of mental illness, no specific diagnosis is required for participation in the registry
- There are no exclusion criteria related to age, sex, or ethnicity
- unable to provide informed consent or does not have an appropriate substitute decision maker that can provide consent on their behalf
- does not speak English or French
Helyszínek itt: Kanada
- Nova Scotia Health AuthorityHalifax, KanadaContact: Jessica Toombs, MScRésztvevőt keres
A vizsgálatról
Mit akar kideríteni a vizsgálat
While effective interventions for depression exist, their success rates are unsatisfactory and their provision is haphazard. The Canadian Depression Research and Intervention Network (CDRIN) Maritimes Depression Hub will improve the delivery of care and the quality of outcomes for youths, adults and seniors with depression across the Maritimes. The investigators will establish an integrated system of assessment, treatment, research and education related to depression with the active involvement of those with lived experience. The establishment of a patient registry is a key step that will facilitate evaluation and reform of current services, integration of patient choice and community resources into treatment programs, monitoring long-term outcomes, and development of more effective treatment approaches through research. The registry will facilitate research that will include validation of new diagnostic and outcome measurement tools, low-cost clinical trials and collaborative projects with national and international partners. Educational programs will involve training the next generation of researchers, those with lived experience, clinicians, and health system managers in critical appraisal and will facilitate their involvement in research. The registry, the proposed systematic measurement of outcomes and the broad dissemination of information and skills will improve the quality of research and of care as well as the experience of patients and their families.
A teljes eredeti leírásKevesebb
The need for a registry: It is increasingly recognized that major advances in the treatment of mental disorders will require large scale clinical research. Recently demonstrated ways of completing large-scale research with finite resources include the routine use of electronic health records (EHR), data linkage and randomized registry trial. Use of EHR is the most efficient way of rapidly obtaining large amounts of information. However, EHR cannot completely exclude confounding by indication and other unmeasured variables. Therefore, tests of treatment effects require experimental designs that cannot be replaced by routine health records data. The gold standard for testing the effects of treatment in an unbiased way is the randomized controlled trial (RCT), where measured and unmeasured confounders are balanced through the randomization process and any remaining confounding is due to chance alone. RCTs are valued as the highest level of evidence, but are costly and take significant time to be completed, partly because of the need to screen a large group of individuals to identify eligible participants.
The most efficient unbiased test of interventions, new treatment modalities and novel ways of treatment delivery is a method that combines EHR use with the randomized controlled trial (RCT) methodology: the randomized registry trial (RRT). The RRT takes advantage of a registry of individuals with available information to identify a large number of individuals suitable for an RCT. The RRT approach is efficient especially if the same information (e.g. diagnosis and treatment history) is used repeatedly for different purposes. The same information can be used for clinical purposes, service improvement and multiple research projects. RRT will allow obtaining answers about the efficacy of new treatments and management strategies significantly faster and at a much lower cost than traditional RCTs. Therefore, the investigators propose to establish a registry that has the capacity to conduct RRTs. The proposed registry will be integrated with similar efforts across Canada. Jointly, this collaborative network of registries will facilitate fast and economical testing of new treatments, which is urgently needed to advance the therapeutic options for people with depression and related conditions.
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakAdatok és források
- Regiszteradat
- Szerepel a ClinicalTrials.gov-on.
- Hivatalos cím
- The Canadian Depression Research and Intervention Network (CDRIN) Maritimes Registry: Reliable Assessment to Enable Research and Improve Clinical Care
- MI-összefoglaló
- A vizsgálat saját részvételi feltételeiből. Gépi kiolvasás: 2026. november 12.
- A regiszteradat frissítve
- 2025. május 14.