ID

37342

Description

Improving Medication Adherence Among Underserved Patients With Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT02409329

Lien

https://clinicaltrials.gov/show/NCT02409329

Mots-clés

  1. 18/07/2019 18/07/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

18 juillet 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Type 2 Diabetes Mellitus NCT02409329

Eligibility Type 2 Diabetes Mellitus NCT02409329

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
adults aged 18 years and older
Description

Adult | Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001675
UMLS CUI [2]
C0001779
individuals who have received a diagnosis for type 2 diabetes mellitus
Description

Diabetes Mellitus, Non-Insulin-Dependent

Type de données

boolean

Alias
UMLS CUI [1]
C0011860
enrolled as a patient at a participating community health center
Description

Study Subject Participation Status | Community Health Center participating

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0009469
UMLS CUI [2,2]
C0679823
individuals currently being treated with oral and/or injectable diabetes medications
Description

Antidiabetics Oral | Antidiabetics Injectable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0935929
UMLS CUI [1,2]
C1527415
UMLS CUI [2,1]
C0935929
UMLS CUI [2,2]
C1828121
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
non-english speakers
Description

Lacking Able to speak English Language

Type de données

boolean

Alias
UMLS CUI [1,1]
C0332268
UMLS CUI [1,2]
C0564215
UMLS CUI [1,3]
C0376245
individuals who report they do not have a cell phone
Description

Cell Phone Lacking

Type de données

boolean

Alias
UMLS CUI [1,1]
C1136359
UMLS CUI [1,2]
C0332268
individuals unwilling and/or not able to provide written informed consent
Description

Informed Consent Unwilling | Informed Consent Unable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
individuals with unintelligible speech (e.g., dysarthria)
Description

Unintelligible Articulation | Dysarthria

Type de données

boolean

Alias
UMLS CUI [1]
C0566625
UMLS CUI [2]
C0013362
individuals with a severe hearing or visual impairment
Description

Severe hearing loss | Severe visual impairment

Type de données

boolean

Alias
UMLS CUI [1]
C3874334
UMLS CUI [2]
C1301509
individuals who report a caregiver administers their diabetes medications individuals who fail the cognitive screener administered during the baseline survey
Description

Caregiver Administration of antibiotic | Recruitment Questionnaire Cognitive failed

Type de données

boolean

Alias
UMLS CUI [1,1]
C0085537
UMLS CUI [1,2]
C0199779
UMLS CUI [2,1]
C0242800
UMLS CUI [2,2]
C0034394
UMLS CUI [2,3]
C1516691
UMLS CUI [2,4]
C0231175
individuals who cannot receive, read, and respond to a text after instruction from a trained research assistant
Description

Patient instructions Research Personnel Unsuccessful

Type de données

boolean

Alias
UMLS CUI [1,1]
C2051542
UMLS CUI [1,2]
C0035173
UMLS CUI [1,3]
C1272705

Similar models

Eligibility Type 2 Diabetes Mellitus NCT02409329

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Adult | Age
Item
adults aged 18 years and older
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Diabetes Mellitus, Non-Insulin-Dependent
Item
individuals who have received a diagnosis for type 2 diabetes mellitus
boolean
C0011860 (UMLS CUI [1])
Study Subject Participation Status | Community Health Center participating
Item
enrolled as a patient at a participating community health center
boolean
C2348568 (UMLS CUI [1])
C0009469 (UMLS CUI [2,1])
C0679823 (UMLS CUI [2,2])
Antidiabetics Oral | Antidiabetics Injectable
Item
individuals currently being treated with oral and/or injectable diabetes medications
boolean
C0935929 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C0935929 (UMLS CUI [2,1])
C1828121 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Lacking Able to speak English Language
Item
non-english speakers
boolean
C0332268 (UMLS CUI [1,1])
C0564215 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
Cell Phone Lacking
Item
individuals who report they do not have a cell phone
boolean
C1136359 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
Informed Consent Unwilling | Informed Consent Unable
Item
individuals unwilling and/or not able to provide written informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Unintelligible Articulation | Dysarthria
Item
individuals with unintelligible speech (e.g., dysarthria)
boolean
C0566625 (UMLS CUI [1])
C0013362 (UMLS CUI [2])
Severe hearing loss | Severe visual impairment
Item
individuals with a severe hearing or visual impairment
boolean
C3874334 (UMLS CUI [1])
C1301509 (UMLS CUI [2])
Caregiver Administration of antibiotic | Recruitment Questionnaire Cognitive failed
Item
individuals who report a caregiver administers their diabetes medications individuals who fail the cognitive screener administered during the baseline survey
boolean
C0085537 (UMLS CUI [1,1])
C0199779 (UMLS CUI [1,2])
C0242800 (UMLS CUI [2,1])
C0034394 (UMLS CUI [2,2])
C1516691 (UMLS CUI [2,3])
C0231175 (UMLS CUI [2,4])
Patient instructions Research Personnel Unsuccessful
Item
individuals who cannot receive, read, and respond to a text after instruction from a trained research assistant
boolean
C2051542 (UMLS CUI [1,1])
C0035173 (UMLS CUI [1,2])
C1272705 (UMLS CUI [1,3])

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