Eligibility Hepatitis C NCT01442311

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
hcv-infected
Description

Hepatitis C

Data type

boolean

Alias
UMLS CUI [1]
C0019196
receive hcv medical care at the methadone clinic
Description

Medical care Hepatitis C Methadone Clinic

Data type

boolean

Alias
UMLS CUI [1,1]
C0496675
UMLS CUI [1,2]
C0019196
UMLS CUI [1,3]
C1552533
plan to initiate hcv treatment on-site within the next 3 months
Description

Therapeutic procedure Hepatitis C Study Site Planned

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0019196
UMLS CUI [1,3]
C2825164
UMLS CUI [1,4]
C1301732
psychiatrically stable as determined by hcv treatment provider and/or on-site psychiatrist
Description

Stable status Psychiatric

Data type

boolean

Alias
UMLS CUI [1,1]
C0205360
UMLS CUI [1,2]
C0205487
attend the methadone clinic between three and six days per week to receive methadone
Description

Methadone Receive days per week

Data type

boolean

Alias
UMLS CUI [1,1]
C0025605
UMLS CUI [1,2]
C1514756
UMLS CUI [1,3]
C0677547
stable dose fo methadone for two weeks prior to the baseline visit
Description

Methadone Dose Stable

Data type

boolean

Alias
UMLS CUI [1,1]
C0025605
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
unable or unwilling to provide informed consent
Description

Informed Consent Unable | Informed Consent Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0558080
currently receiving hcv treatment
Description

Therapeutic procedure Hepatitis C

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0019196
primary hcv care provider does not agree to their participation in the trial
Description

Participation Clinical Trial Refused

Data type

boolean

Alias
UMLS CUI [1,1]
C0679823
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C1705116
psychiatrically unstable
Description

Unstable status Psychiatric

Data type

boolean

Alias
UMLS CUI [1,1]
C0443343
UMLS CUI [1,2]
C0205487

Similar models

Eligibility Hepatitis C NCT01442311

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Hepatitis C
Item
hcv-infected
boolean
C0019196 (UMLS CUI [1])
Medical care Hepatitis C Methadone Clinic
Item
receive hcv medical care at the methadone clinic
boolean
C0496675 (UMLS CUI [1,1])
C0019196 (UMLS CUI [1,2])
C1552533 (UMLS CUI [1,3])
Therapeutic procedure Hepatitis C Study Site Planned
Item
plan to initiate hcv treatment on-site within the next 3 months
boolean
C0087111 (UMLS CUI [1,1])
C0019196 (UMLS CUI [1,2])
C2825164 (UMLS CUI [1,3])
C1301732 (UMLS CUI [1,4])
Stable status Psychiatric
Item
psychiatrically stable as determined by hcv treatment provider and/or on-site psychiatrist
boolean
C0205360 (UMLS CUI [1,1])
C0205487 (UMLS CUI [1,2])
Methadone Receive days per week
Item
attend the methadone clinic between three and six days per week to receive methadone
boolean
C0025605 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C0677547 (UMLS CUI [1,3])
Methadone Dose Stable
Item
stable dose fo methadone for two weeks prior to the baseline visit
boolean
C0025605 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Informed Consent Unable | Informed Consent Unwilling
Item
unable or unwilling to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Therapeutic procedure Hepatitis C
Item
currently receiving hcv treatment
boolean
C0087111 (UMLS CUI [1,1])
C0019196 (UMLS CUI [1,2])
Participation Clinical Trial Refused
Item
primary hcv care provider does not agree to their participation in the trial
boolean
C0679823 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C1705116 (UMLS CUI [1,3])
Unstable status Psychiatric
Item
psychiatrically unstable
boolean
C0443343 (UMLS CUI [1,1])
C0205487 (UMLS CUI [1,2])