- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07826819
Consensus on Low-resource Setting Definition: An inteRnational Delphi sTudY (CLARITY-LRS) (CLARITY-LRS)
Studieoversigt
Status
Undersøgelsestype
Tilmelding (Anslået)
Kontakter og lokationer
Studiekontakt
- Navn: Pedja Kovacevic, MD,PhD
- Telefonnummer: 051342507
- E-mail: peko051@yahoo.com
Studiesteder
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The Repblic of Srpska
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Banja Luka, The Repblic of Srpska, Bosnien-Hercegovina, 78000
- University Clinical Centre of the Republic of Srpska
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Kontakt:
- Pedja Kovacevic
- Telefonnummer: 051342507
- E-mail: peko051@yahoo.com
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
Adults aged 18 years or older. Healthcare professionals, researchers, policymakers, health system experts, patient representatives, or other stakeholders with relevant knowledge or experience related to healthcare delivery, critical care, global health, health systems, or resource-limited healthcare environments.
Ability to read and understand English. Willingness to provide informed consent and participate in the Delphi process. Access to the internet and ability to complete electronic questionnaires. -
Exclusion Criteria:
Individuals younger than 18 years. Individuals without relevant professional, research, policy, health-system, or lived experience related to the study topic.
Inability to understand the study information or complete the questionnaires in English.
Refusal or inability to provide informed consent. Failure to complete the initial Delphi questionnaire round.
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Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Number and proportion of candidate statements rated 7-9 on the 9-point Likert scale
Tidsramme: From the first Delphi round through completion of the final Delphi round, up to 12 months
|
International Delphi panelists will rate each candidate statement on a 9-point Likert scale, where 1 indicates strong disagreement and 9 indicates strong agreement.
Consensus for inclusion in the low-resource setting definition will be defined as at least 80% of respondents rating a statement from 7 to 9. The outcome will be summarized as the number and percentage of candidate statements meeting this prespecified consensus threshold after completion of the Delphi process.
|
From the first Delphi round through completion of the final Delphi round, up to 12 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Number and proportion of candidate statements with stable ratings between consecutive Delphi rounds
Tidsramme: From completion of the first Delphi round through completion of the final Delphi round, up to 12 months
|
Stability of ratings will be assessed among panelists who participate in consecutive Delphi rounds.
Ratings assigned using the 9-point Likert scale will be compared between consecutive rounds using the Wilcoxon signed-rank test.
The outcome will be reported as the number and proportion of candidate statements for which no statistically significant change in ratings is observed between consecutive rounds.
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From completion of the first Delphi round through completion of the final Delphi round, up to 12 months
|
Samarbejdspartnere og efterforskere
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
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
Andre undersøgelses-id-numre
- 01-19-420-2/26
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
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