Informatie:
Fout:
ID
39975
Beschrijving
Effectiveness of SMS Text Reminders to Improve Blood Pressure Among Patients With Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01255436
Link
https://clinicaltrials.gov/show/NCT01255436
Trefwoorden
Versies (1)
- 07-03-20 07-03-20 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
7 maart 2020
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hypertension NCT01255436
Eligibility Hypertension NCT01255436
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT01255436
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Outpatients | Adult | Age
Item
ambulatory adult patients of both sexes with age at least 19 years old being seen at the general medicine outpatient clinic of the philippine general hospital
boolean
C0029921 (UMLS CUI [1])
C0001675 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
C0001675 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
Hypertensive disease
Item
a diagnosis of hypertension in the medical record
boolean
C0020538 (UMLS CUI [1])
Pharmaceutical Preparation Quantity Hypertensive disease | Maintenance therapy
Item
on at least 1 maintenance medication for hypertension for at least 1 month
boolean
C0013227 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0020538 (UMLS CUI [1,3])
C0677908 (UMLS CUI [2])
C1265611 (UMLS CUI [1,2])
C0020538 (UMLS CUI [1,3])
C0677908 (UMLS CUI [2])
Systolic Pressure | Diastolic blood pressure
Item
a systolic blood pressure greater than 129 mmhg and less than 160 mmhg or a diastolic blood pressure greater than 79 mmhg or less than 100 mmhg at the time of screening
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
C0428883 (UMLS CUI [2])
Access Mobile Phone
Item
patients with daily access to a mobile phone in the household
boolean
C0444454 (UMLS CUI [1,1])
C1136360 (UMLS CUI [1,2])
C1136360 (UMLS CUI [1,2])
Use of Text Messages Mobile Phone
Item
patients who live with someone who knows how to retrieve and read text messages on their mobile phone, and can relay these messages to them
boolean
C1524063 (UMLS CUI [1,1])
C3178910 (UMLS CUI [1,2])
C1136360 (UMLS CUI [1,3])
C3178910 (UMLS CUI [1,2])
C1136360 (UMLS CUI [1,3])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Study Subject Participation Status | Clinical Trial
Item
participation in other studies within one month of trial initiation
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2])
C0008976 (UMLS CUI [2])
Informed Consent Unable | Informed Consent Refused
Item
patients who are unable or refuse to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Medical condition Interferes with Clinical Trial | Dementia | Psychological disease
Item
patients who have a clinical condition that might interfere with the study (dementia, psychological disorder)
boolean
C3843040 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0497327 (UMLS CUI [2])
C1658764 (UMLS CUI [3])
C0521102 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0497327 (UMLS CUI [2])
C1658764 (UMLS CUI [3])
Study Subject Participation Status | Research Subject Recruitment Patient Other
Item
patients who share a household with another patient who has already been recruited to participate in this study
boolean
C2348568 (UMLS CUI [1])
C0376425 (UMLS CUI [2,1])
C0030705 (UMLS CUI [2,2])
C0205394 (UMLS CUI [2,3])
C0376425 (UMLS CUI [2,1])
C0030705 (UMLS CUI [2,2])
C0205394 (UMLS CUI [2,3])