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ID
17394
Beschrijving
n-3 PUFA for Vascular Cognitive Aging; ODM derived from: https://clinicaltrials.gov/show/NCT01953705
Link
https://clinicaltrials.gov/show/NCT01953705
Trefwoorden
Versies (1)
- 11-09-16 11-09-16 -
Geüploaded op
11 september 2016
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Age Related Cognitive Decline NCT01953705
Eligibility Age Related Cognitive Decline NCT01953705
- StudyEvent: Eligibility
Similar models
Eligibility Age Related Cognitive Decline NCT01953705
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
cognitive impairment
Item
non-demented or mild cognitive impairment, defined as clinical dementia rating =0 or 0.5.
boolean
C0338656 (UMLS CUI [1])
age, sex
Item
age 80 and older, male and female
boolean
C0001779 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
C0079399 (UMLS CUI [2])
wmh volume
Item
total wmh volume ≥ 6 cc (>80% of our oregon brain aging study population meets this criterion)
boolean
C0682708 (UMLS CUI [1,1])
C0449468 (UMLS CUI [1,2])
C0449468 (UMLS CUI [1,2])
plasma pufa
Item
plasma pufa (epa + dha) < 110 ug/ml or < 5 weight percent (>85% of our obas population meets this)
boolean
C0032615 (UMLS CUI [1,1])
C0032105 (UMLS CUI [1,2])
C0032105 (UMLS CUI [1,2])
english language skills
Item
sufficient english language skills to complete all tests
boolean
C0376245 (UMLS CUI [1])
geriatric depression scale
Item
geriatric depression scale - 15 < 6 documenting absence of a significant depressive syndrome
boolean
C0451184 (UMLS CUI [1])
vision and hearing
Item
sufficient vision and hearing to complete all tests
boolean
C2706921 (UMLS CUI [1])
functional status
Item
informant available with frequent (at least 1 hour/day or 1 day/week) contact with subject to verify functional status and cdr rating
boolean
C0598463 (UMLS CUI [1])
health status
Item
general health status that will not interfere with the ability to complete the prospective study (these conditions are listed below in the study exclusion list)
boolean
C0018759 (UMLS CUI [1])
dementing illness
Item
any dementing illness (ad, vascular dementia, normal pressure hydrocephalus, or parkinson's disease); dementia defined by cdr ≥ 1
boolean
C0497327 (UMLS CUI [1])
cns disease
Item
significant disease of the cns such as brain tumor, seizure disorder, subdural hematoma, cranial arteritis
boolean
C0007682 (UMLS CUI [1])
substance abuse
Item
alcohol or substance abuse according to dsm-iv criteria within the last 2 years
boolean
C0038586 (UMLS CUI [1])
psychiatric disorder
Item
major depression, schizophrenia, or other major psychiatric disorder defined by dsm-iv criteria
boolean
C0004936 (UMLS CUI [1])
b12 deficiency
Item
abnormal labs indicating vitamin b12 deficiency, thyroid disease, or uti (documented bacterial colonization is acceptable)
boolean
C0042847 (UMLS CUI [1])
cvd
Item
unstable or significantly symptomatic cvd (e.g. cad with frequent angina, chf with dyspnea at rest)
boolean
C0007222 (UMLS CUI [1])
hypertension
Item
hypertension: either 1) blood pressure > 150/90 or 2) > 2 medications to control
boolean
C0020538 (UMLS CUI [1])
orthostatic hypotension
Item
clinical symptomatic orthostatic hypotension
boolean
C0020651 (UMLS CUI [1])
diabetes mellitus
Item
diabetes mellitus that requires insulin injections
boolean
C0011849 (UMLS CUI [1])
cortical stroke
Item
history of cortical stroke
boolean
C0038454 (UMLS CUI [1])
cancer
Item
cancer within the last 5 years, with the exception of localized prostate cancer (gleason grade < 3) and non-metastatic skin cancers (melanoma).
boolean
C0006826 (UMLS CUI [1])
illness
Item
illness that requires >1 visit /month to a clinician
boolean
C0221423 (UMLS CUI [1])
vision loss
Item
progressive vision loss (age-related macular degeneration already beginning to degrade vision)
boolean
C3665347 (UMLS CUI [1])
contraindications to mri
Item
contraindications to mri (i.e., heart pacemaker, metal plates or objects in head, metal worker)
boolean
C0079164 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,2])
analgesics
Item
analgesics: frequent use of high doses
boolean
C0002771 (UMLS CUI [1])
sedatives
Item
sedatives: except for those used occasionally for sleep (use limited to ≤ twice per week)
boolean
C0036557 (UMLS CUI [1])
cns active meds
Item
cns active meds that have not been on stable doses for at least 2 months (cimetidine, beta-blockers, and ssris)
boolean
C1874882 (UMLS CUI [1])
active hypertension
Item
active hypertension on > 2 meds or using cns active agents (propranolol or clonidine)
boolean
C0020538 (UMLS CUI [1])
neuroleptics
Item
neuroleptics, antiparkinsonian agents, systemic corticosteroids, and narcotic analgesics; in the case where these were used for a self-limited time they must have been discounted for a period of five half-lives prior to baseline visit
boolean
C0040615 (UMLS CUI [1])
supplements
Item
over the counter supplements are not by themselves exclusionary, however, subjects are asked not to change the dosing regimen over the course of the trial unless medically indicated; the presence and dose of these agents are recorded
boolean
C0242295 (UMLS CUI [1])
omega 3
Item
taking omega 3 pufa supplements and a screen plasma pufa > 5 weight percent of total fatty acids for epa+dha will confirm supplementation of o3pufa history
boolean
C0015689 (UMLS CUI [1])
cholinesterase inhibitor
Item
cholinesterase inhibitors (i.e., aricept)
boolean
C0008425 (UMLS CUI [1])
investigational drug
Item
investigational drugs within five half-lives prior to baseline
boolean
C0013230 (UMLS CUI [1])
anticoagulation therapy
Item
anticoagulation therapy: vitamin k agonist, warfarin, factor xa inhibitors, low molecular weight heparins.
boolean
C0003281 (UMLS CUI [1])