ID

29507

Descrição

Coventry Outcomes Study of Seniors (COSS): A Comparative Effectiveness Study to Evaluate the Effect of a Multidisciplinary Team's Intervention on the Incidence of Nonelective Hospitalizations in a Medicare Population; ODM derived from: https://clinicaltrials.gov/show/NCT01014884

Link

https://clinicaltrials.gov/show/NCT01014884

Palavras-chave

  1. 04/04/2018 04/04/2018 -
Titular dos direitos

See clinicaltrials.gov

Transferido a

4 de abril de 2018

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0

Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Heart Failure NCT01014884

Eligibility Heart Failure NCT01014884

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
inouye risk score >3 calculated on coventry claims
Descrição

Other Coding

Tipo de dados

boolean

Alias
UMLS CUI [1]
C3846158
medicare advantage beneficiaries age > 65 years
Descrição

Medicare Advantage Beneficiary Age

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C2713369
UMLS CUI [1,2]
C3853043
UMLS CUI [1,3]
C0001779
continuous eligibility > 12 months prior to study
Descrição

Eligibility Duration

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1548635
UMLS CUI [1,2]
C0449238
ability to be contacted via telephone
Descrição

Ability Telephone Contact

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0085732
UMLS CUI [1,2]
C0039457
UMLS CUI [1,3]
C0332158
subject is willing and able to provide informed consent
Descrição

Informed Consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
willing to comply with all study procedures and be available for the duration of the study
Descrição

Protocol Compliance

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
active cancer treatment (i.e. chemotherapy or radiation) in the past 6 months
Descrição

Cancer treatment | Chemotherapy | Therapeutic radiology procedure

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0920425
UMLS CUI [2]
C0392920
UMLS CUI [3]
C1522449
living anywhere other than a community setting [i.e. skilled nursing facility (snf)]
Descrição

Skilled nursing facility

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0037265
just-in-time (jit) members
Descrição

Just-in-time member

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1517626
UMLS CUI [1,2]
C0680022
members with a geographic location > 60 from either st. louis or kansas city, mo.
Descrição

Members Geographic Location

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0680022
UMLS CUI [1,2]
C0017446
solid organ transplant recipients
Descrição

Solid organ transplant Recipient

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0730400
UMLS CUI [1,2]
C1709854
active enrollment in another clinical research study
Descrição

Study Subject Participation Status

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Heart Failure NCT01014884

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Other Coding
Item
inouye risk score >3 calculated on coventry claims
boolean
C3846158 (UMLS CUI [1])
Medicare Advantage Beneficiary Age
Item
medicare advantage beneficiaries age > 65 years
boolean
C2713369 (UMLS CUI [1,1])
C3853043 (UMLS CUI [1,2])
C0001779 (UMLS CUI [1,3])
Eligibility Duration
Item
continuous eligibility > 12 months prior to study
boolean
C1548635 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Ability Telephone Contact
Item
ability to be contacted via telephone
boolean
C0085732 (UMLS CUI [1,1])
C0039457 (UMLS CUI [1,2])
C0332158 (UMLS CUI [1,3])
Informed Consent
Item
subject is willing and able to provide informed consent
boolean
C0021430 (UMLS CUI [1])
Protocol Compliance
Item
willing to comply with all study procedures and be available for the duration of the study
boolean
C0525058 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Cancer treatment | Chemotherapy | Therapeutic radiology procedure
Item
active cancer treatment (i.e. chemotherapy or radiation) in the past 6 months
boolean
C0920425 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C1522449 (UMLS CUI [3])
Skilled nursing facility
Item
living anywhere other than a community setting [i.e. skilled nursing facility (snf)]
boolean
C0037265 (UMLS CUI [1])
Just-in-time member
Item
just-in-time (jit) members
boolean
C1517626 (UMLS CUI [1,1])
C0680022 (UMLS CUI [1,2])
Members Geographic Location
Item
members with a geographic location > 60 from either st. louis or kansas city, mo.
boolean
C0680022 (UMLS CUI [1,1])
C0017446 (UMLS CUI [1,2])
Solid organ transplant Recipient
Item
solid organ transplant recipients
boolean
C0730400 (UMLS CUI [1,1])
C1709854 (UMLS CUI [1,2])
Study Subject Participation Status
Item
active enrollment in another clinical research study
boolean
C2348568 (UMLS CUI [1])

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial