Inglês

Eligibility Criteria

5 Formulários  
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. This subject consent data table includes subject IDs, consent group information, and subject aliases.
    3. This subject sample mapping data table includes a mapping of study subject IDs to sample IDs and sample aliases. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs.
    4. This subject phenotypes data table includes participants who have completed questionnaires regarding medical history, medications, physical activity, diet, alcohol intake, and cigarette smoking. Objective measures of anthropometric, neuromuscular, vision, strength, and cognitive variables were obtained at a clinic visit. Skeletal assessments included DEXA of the total hip, femoral neck and lumbar spine, calcaneal ultrasound, and vertebral radiographs. Radiographic prevalent and incident vertebral (baseline to visit 3) fractures were assessed. Sleep characteristics were assessed in a subcohort with actigraphy and polysomnography. Radiographic hip osteoarthritis was measured using hip X-rays collected at the SOF baseline visit and a modified Croft summary grade for radiographic hip OA (RHOA) severity of 0 - 4 was assigned to each hip based on individual radiographic features. Both SOF and MrOS data contain harmonized variables with the prefix HA to allow sex differences to be evaluated.
    5. This sample attributes data table includes body site where sample was collected, analyte type, and tumor status.
Inclusion and exclusion criteria
Descrição

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C1512693
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.
Descrição

Elig.phs000510.v1.p1.1

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C3846158
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 measures.
Descrição

Elig.phs000510.v1.p1.2

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C3846158
The SOF study recruited only women.
Descrição

Elig.phs000510.v1.p1.3

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C3846158
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Similar models

Eligibility Criteria

5 Formulários
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. This subject consent data table includes subject IDs, consent group information, and subject aliases.
    3. This subject sample mapping data table includes a mapping of study subject IDs to sample IDs and sample aliases. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs.
    4. This subject phenotypes data table includes participants who have completed questionnaires regarding medical history, medications, physical activity, diet, alcohol intake, and cigarette smoking. Objective measures of anthropometric, neuromuscular, vision, strength, and cognitive variables were obtained at a clinic visit. Skeletal assessments included DEXA of the total hip, femoral neck and lumbar spine, calcaneal ultrasound, and vertebral radiographs. Radiographic prevalent and incident vertebral (baseline to visit 3) fractures were assessed. Sleep characteristics were assessed in a subcohort with actigraphy and polysomnography. Radiographic hip osteoarthritis was measured using hip X-rays collected at the SOF baseline visit and a modified Croft summary grade for radiographic hip OA (RHOA) severity of 0 - 4 was assigned to each hip based on individual radiographic features. Both SOF and MrOS data contain harmonized variables with the prefix HA to allow sex differences to be evaluated.
    5. This sample attributes data table includes body site where sample was collected, analyte type, and tumor status.
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Inclusion and exclusion criteria
C0680251 (UMLS CUI [1,1])
C1512693 (UMLS CUI [1,2])
Elig.phs000510.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
C3846158 (UMLS CUI [1,1])
Elig.phs000510.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 measures.
boolean
C3846158 (UMLS CUI [1,1])
Elig.phs000510.v1.p1.3
Item
The SOF study recruited only women.
boolean
C3846158 (UMLS CUI [1,1])
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