Elig.phs000373.v1.p1.1
Item
The inclusion criteria were: 1) 65 years or older, (2) ability to walk without the assistance of another, (3) absence of bilateral hip replacements, (4) ability to provide self-reported data, (5) residence near a clinical site for the duration of the study, (6) absence of a medical condition that (in the judgment of the investigator) would result in imminent death, and (7) ability to understand and sign an informed consent.
boolean
C1512693 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
C4722228 (UMLS CUI [1,3])
C1298908 (UMLS CUI [1,4])
C2732563 (UMLS CUI [1,5])
C0681906 (UMLS CUI [1,6])
C1830482 (UMLS CUI [1,7])
C2347790 (UMLS CUI [1,8])
C1298908 (UMLS CUI [1,9])
C4745084 (UMLS CUI [1,10])
C0332294 (UMLS CUI [1,11])
C2363727 (UMLS CUI [1,12])
C4304770 (UMLS CUI [1,13])
Elig.phs000373.v1.p1.2
Item
To qualify as an enrollee, the participant had to provide written informed consent, complete the self-administered questionnaire (SAQ), attend the clinic visit, and complete at least the anthropometric, DXA (for the MrOS cohort), and vertebral X-ray procedures.
boolean
C0021430 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0034394 (UMLS CUI [1,3])
C0008952 (UMLS CUI [1,4])
C1999232 (UMLS CUI [1,5])
C0205197 (UMLS CUI [1,6])
C0815129 (UMLS CUI [1,7])
C4537707 (UMLS CUI [1,8])
C0203139 (UMLS CUI [1,9])
Elig.phs000373.v1.p1.3
Item
The MrOS cohort recruited only men.
boolean
C0086582 (UMLS CUI [1,1])