ID

34370

Descrição

Feasibility Study of an Intervention Therapeutic Education for Patients Treated With Androgen Deprivation; ODM derived from: https://clinicaltrials.gov/show/NCT02460549

Link

https://clinicaltrials.gov/show/NCT02460549

Palavras-chave

  1. 16/01/2019 16/01/2019 -
Titular dos direitos

See clinicaltrials.gov

Transferido a

16 de janeiro de 2019

DOI

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Licença

Creative Commons BY 4.0

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Eligibility Prostate Cancer NCT02460549

Eligibility Prostate Cancer NCT02460549

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients supported in consultation urology at the university hospital north saint etienne.
Descrição

Consultation Urology

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0009818
UMLS CUI [1,2]
C0042077
aged over 18 years
Descrição

Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
having an evolutive prostate cancer
Descrição

Prostate carcinoma Developmental

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0600139
UMLS CUI [1,2]
C0458003
patient treated with lhrh agonist for at least 6 months - affiliated with the national health insurance system
Descrição

LHRH Agonist | Patient Affiliated National Health Insurance

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1518041
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C1510826
UMLS CUI [2,3]
C0027452
and having completed the worksheet informed consent to participate in the program.
Descrição

Informed Consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
refusal of participation, protected or under guardianship patients.
Descrição

Refusal to Participate | Protection of patient | Guardianship of Patient

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1136454
UMLS CUI [2]
C0412786
UMLS CUI [3,1]
C0680611
UMLS CUI [3,2]
C0030705
patients unable to understand the study or unable to follow the educational sessions.
Descrição

Study Protocol Comprehension Unable | Educational session with patient Unsuccessful

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0162340
UMLS CUI [1,3]
C1299582
UMLS CUI [2,1]
C1276369
UMLS CUI [2,2]
C1272705
patient (s) with documented cognitive or psychiatric history.
Descrição

Impaired cognition | Mental disorders

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0338656
UMLS CUI [2]
C0004936
geographical remotness (more than 100 kms.)
Descrição

Residence Remote

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C0205157

Similar models

Eligibility Prostate Cancer NCT02460549

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Consultation Urology
Item
patients supported in consultation urology at the university hospital north saint etienne.
boolean
C0009818 (UMLS CUI [1,1])
C0042077 (UMLS CUI [1,2])
Age
Item
aged over 18 years
boolean
C0001779 (UMLS CUI [1])
Prostate carcinoma Developmental
Item
having an evolutive prostate cancer
boolean
C0600139 (UMLS CUI [1,1])
C0458003 (UMLS CUI [1,2])
LHRH Agonist | Patient Affiliated National Health Insurance
Item
patient treated with lhrh agonist for at least 6 months - affiliated with the national health insurance system
boolean
C1518041 (UMLS CUI [1])
C0030705 (UMLS CUI [2,1])
C1510826 (UMLS CUI [2,2])
C0027452 (UMLS CUI [2,3])
Informed Consent
Item
and having completed the worksheet informed consent to participate in the program.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Refusal to Participate | Protection of patient | Guardianship of Patient
Item
refusal of participation, protected or under guardianship patients.
boolean
C1136454 (UMLS CUI [1])
C0412786 (UMLS CUI [2])
C0680611 (UMLS CUI [3,1])
C0030705 (UMLS CUI [3,2])
Study Protocol Comprehension Unable | Educational session with patient Unsuccessful
Item
patients unable to understand the study or unable to follow the educational sessions.
boolean
C2348563 (UMLS CUI [1,1])
C0162340 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C1276369 (UMLS CUI [2,1])
C1272705 (UMLS CUI [2,2])
Impaired cognition | Mental disorders
Item
patient (s) with documented cognitive or psychiatric history.
boolean
C0338656 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
Residence Remote
Item
geographical remotness (more than 100 kms.)
boolean
C0237096 (UMLS CUI [1,1])
C0205157 (UMLS CUI [1,2])

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