ID

40323

Description

Efficiency of Monitoring and Control Program of Hypertension Through Pharmacy Offices. APOF Project; ODM derived from: https://clinicaltrials.gov/show/NCT02032472

Lien

https://clinicaltrials.gov/show/NCT02032472

Mots-clés

Versions (1)
  1. 08/04/2020 08/04/2020 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

8 avril 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Hypertension NCT02032472

Anglais

Eligibility Hypertension NCT02032472

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age not less than 18 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
hta controlled over 2 years of evolution
Description

Hypertensive disease Controlled Duration

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C2911690
UMLS CUI [1,3]
C0449238
subjects with a history open to participating health centers or stable residence in the geographic area
Description

Medical History Participation Health center | Residence Stable Geographic area

Type de données

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C0475309
UMLS CUI [2,1]
C0237096
UMLS CUI [2,2]
C0205360
UMLS CUI [2,3]
C0017446
subjects who agree to participate
Description

Study Subject Participation Status Agreement

Type de données

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0680240
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
comorbidity and concomitant (diabetes mellitus, heart failure or renal failure
Description

Comorbidity | Diabetes Mellitus | Heart failure | Kidney Failure

Type de données

boolean

Alias
UMLS CUI [1]
C0009488
UMLS CUI [2]
C0011849
UMLS CUI [3]
C0018801
UMLS CUI [4]
C0035078
patients with temporary residence in the geographic area of study
Description

Residence Temporary | Geographic area Clinical Trial

Type de données

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C0205374
UMLS CUI [2,1]
C0017446
UMLS CUI [2,2]
C0008976
subjects of hypertension controlled by outside professionals to our primary care teams.
Description

Hypertensive disease Controlled by Health Professionals

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0332298
UMLS CUI [1,3]
C1704312
subjects with home care or any other cause which does not permit their displacement, transfer to the clinic or pharmacy during the evaluation period.
Description

Home care of patient | Patient Transfer Clinic Unsuccessful

Type de données

boolean

Alias
UMLS CUI [1]
C0204977
UMLS CUI [2,1]
C0030704
UMLS CUI [2,2]
C0442592
UMLS CUI [2,3]
C1272705
subjects with severe diseases of poor prognosis, hopefully less than one year of life.
Description

Disease Severe | Prognosis bad | Life Expectancy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0278252
UMLS CUI [3]
C0023671
subjects who do not have telephones.
Description

Telephone Lacking

Type de données

boolean

Alias
UMLS CUI [1,1]
C0039457
UMLS CUI [1,2]
C0332268
subjects with communication problems (cognitive impairment, sensory, language barrier)
Description

Communication impairment | Impaired cognition | Hypesthesia | Language Barriers

Type de données

boolean

Alias
UMLS CUI [1]
C0009460
UMLS CUI [2]
C0338656
UMLS CUI [3]
C0020580
UMLS CUI [4]
C0237167
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Similar models

Eligibility Hypertension NCT02032472

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age not less than 18 years
boolean
C0001779 (UMLS CUI [1])
Hypertensive disease Controlled Duration
Item
hta controlled over 2 years of evolution
boolean
C0020538 (UMLS CUI [1,1])
C2911690 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Medical History Participation Health center | Residence Stable Geographic area
Item
subjects with a history open to participating health centers or stable residence in the geographic area
boolean
C0262926 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0475309 (UMLS CUI [1,3])
C0237096 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
C0017446 (UMLS CUI [2,3])
Study Subject Participation Status Agreement
Item
subjects who agree to participate
boolean
C2348568 (UMLS CUI [1,1])
C0680240 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Comorbidity | Diabetes Mellitus | Heart failure | Kidney Failure
Item
comorbidity and concomitant (diabetes mellitus, heart failure or renal failure
boolean
C0009488 (UMLS CUI [1])
C0011849 (UMLS CUI [2])
C0018801 (UMLS CUI [3])
C0035078 (UMLS CUI [4])
Residence Temporary | Geographic area Clinical Trial
Item
patients with temporary residence in the geographic area of study
boolean
C0237096 (UMLS CUI [1,1])
C0205374 (UMLS CUI [1,2])
C0017446 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
Hypertensive disease Controlled by Health Professionals
Item
subjects of hypertension controlled by outside professionals to our primary care teams.
boolean
C0020538 (UMLS CUI [1,1])
C0332298 (UMLS CUI [1,2])
C1704312 (UMLS CUI [1,3])
Home care of patient | Patient Transfer Clinic Unsuccessful
Item
subjects with home care or any other cause which does not permit their displacement, transfer to the clinic or pharmacy during the evaluation period.
boolean
C0204977 (UMLS CUI [1])
C0030704 (UMLS CUI [2,1])
C0442592 (UMLS CUI [2,2])
C1272705 (UMLS CUI [2,3])
Disease Severe | Prognosis bad | Life Expectancy
Item
subjects with severe diseases of poor prognosis, hopefully less than one year of life.
boolean
C0012634 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0278252 (UMLS CUI [2])
C0023671 (UMLS CUI [3])
Telephone Lacking
Item
subjects who do not have telephones.
boolean
C0039457 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Communication impairment | Impaired cognition | Hypesthesia | Language Barriers
Item
subjects with communication problems (cognitive impairment, sensory, language barrier)
boolean
C0009460 (UMLS CUI [1])
C0338656 (UMLS CUI [2])
C0020580 (UMLS CUI [3])
C0237167 (UMLS CUI [4])
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