Engels

The data table (n=16 variables) contains information about AREDS participants' general vision status (e.g. general vision score, ocular pain score, VFQ overall score), and its effect on participants' behavior (e.g. near and distant activities, social activities, driving, mental health score) as obtained through the VFQ-25 questionnaire. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.

19 Formulieren  
  1. StudyEvent: NEI Age-Related Eye Disease Study (AREDS)
    1. Eligibility Criteria
    2. The data table (n=142 variables) contains AMD and cataract phenotype information, medical history and socio-demographic information drawn from several data sets (e.g. enrollment_randomization, amdlensphenotype, followup), plus a unique patient identifier (ID2) for participants with a genetic specimen (to be found only in GENSPECPHENOTYPE and GENSPECFUNDUSLENS [pht000376] tables). Nuclear, cortical and posterior subcapsular opacity information is included for both eyes at baseline and end of study. Other disease information (e.g. diabetes, cancer, angina), medical information (e.g. BMI, blood pressure) and smoking status are also included annually throughout follow-up.
    3. The data table (n=12 variables) contains information about the occurrence of adverse events during the AREDS clinical trial, e.g. type of adverse event, severity, primary ICD9 code, outcome, potential relationship to study drug, timing, and treatment. Data were collected through the clinical trial and for the first 6 months of the natural history follow-up immediately after the clinical trial concluded. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    4. The data table (n=25 variables) contains detailed information about cataract phenotypes (n=23 variables) as well as final AMD phenotype (n=1 variable), and patient ID. Nuclear, cortical and posterior subcapsular opacity information is included for both eyes at baseline and end of study. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    5. The data table (n=56 variables) contains information about AREDS participants' dietary intake of alcohol, amino acids, carbohydrates, fiber, poly- and monounsaturated fatty acids, proteins, vitamins and minerals. Participants' glycemic index and glycemic load are also included. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    6. The data table (n=102 variables) contains AREDS treatment assignment, basic socio-demographic characteristics and baseline medical history for AREDS participants. Medical history information includes eye disease information such as AMD Category, visual acuity, and past ophthalmic treatments (e.g. cataract surgery, laser treatment), as well as information about the presence/absence of other diseases (e.g. angina, arthritis, cancer, diabetes, high blood pressure), use of prescribed drugs for disease management (e.g. blood-thinning medications, digoxin, thyroid hormones, insulin), use of over-the-counter drugs (e.g. NSAIDs, antacids), intake of vitamins and minerals, and smoking history. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    7. The data table (n=83 variables) contains information obtained at follow-up visits during the AREDS clinical trial (every six months following randomization), annually in person during the natural history follow-up, and via phone between annual in-person visits. Variables include information about AREDS participants' ophthalmic medical history (e.g. cataract or other eye surgery, laser treatment for AMD, retinal repair, capsulotomy, presence/absence of lens, glaucoma, and visual acuity) and general medical information, including new diagnoses of cancer, heart disease, stroke, and peripheral vascular disease, disease history of angina and high blood pressure, current disease status of diabetes, arthritis, and gout, use of prescribed drugs for disease treatment or management (e.g. blood-thinning medications, digoxin, thyroid hormones, insulin), use of over-the-counter drugs (e.g. NSAIDs, antacids), and smoking behavior. For version 3 release of the study, visual acuity data of the right eye have been added for odd-numbered visits. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    8. The data table (n=49 variables) contains information from AREDS participants' fundus photographs, including presence, type, and extent of drusen, presence/extent of RPE depigmentation, SSR (serous sensory retinal) detachments, subretinal hemorrhages, subretinal fibrosis, and geographic atrophy. In addition, information on photocoagulation (PC) treatment for AMD SRNV is included, as well as AMD Severity Scale Scores and AMD Simple Scale Scores calculated from the fundus data. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    9. The data table (n=62) contains information only for AREDS participants who have a genetic specimen. A unique patient identifier (ID2 field) for these participants (to be found only in GENSPECPHENOTYPE [pht000001.v2.p1] and GENSPECFUNDUSLENS data tables) is included instead of the patient identifier used for data tables with all participants (ID field). Information about fundus and lens characteristics are included as follows - fundus: presence, type, and extent of drusen, presence/extent of RPE depigmentation, SSR (serous sensory retinal) detachments, subretinal hemorrhages, subretinal fibrosis, and geographic atrophy; lens: degree of nuclear sclerosis, cortical and posterior subcapsular opacities, and iris pigmentation. In addition, information on photocoagulation (PC) treatment for AMD is included as well as AMD Severity Scale Scores and AMD Simple Scale Scores calculated from the fundus data.
    10. The data table (n=6 variables) contains information about AREDS participant hospitalizations (e.g. reason, time from randomization, duration, primary ICD9 code) during the entire study. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    11. The data table (n=21 variables) contains information from AREDS participants' lens photographs, including degree of nuclear sclerosis, cortical and posterior subcapsular opacities, and iris pigmentation. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    12. The data table (n=7 variables) contains information about AREDS participant deaths (e.g. cause, time from randomization) during the entire study. A search using the National Death Index (NDI) yielded additional deaths not identified during the study. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    13. The data table (n=44 variables) contains information about AREDS participants' use (e.g. type, frequency, dose, duration) of non-steroidal anti-inflammatory drugs (e.g. aspirin, ibuprofen, acetaminophen, naproxen). Data were collected at in-clinic visits starting in October 2004. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    14. The data table (n=16 variables) contains information about AREDS participants' general vision status (e.g. general vision score, ocular pain score, VFQ overall score), and its effect on participants' behavior (e.g. near and distant activities, social activities, driving, mental health score) as obtained through the VFQ-25 questionnaire. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    15. Subject - Consent Information
    16. Subject - Sample Mapping (including mapping to Coriell IDs)
    17. The data table (n=2 variables) contains information on subjects' annual exposure to sunlight (hours; April through September).
    18. This dataset provides refractive error values obtained from control subjects of the AREDS study (phs000001.v3.p1) and represents a substudy of AREDS ; data of n=7 new variables are provided in addition to basic sociodemographic data. Subject - consent and subject - sample mapping information is available through phs000001.v3.p1.
    19. This dataset provides refractive error values obtained from control subjects of the AREDS study (phs000001.v3.p1) and represents a substudy of AREDS ; data of n=7 new variables are provided in addition to basic sociodemographic data. Subject - consent and subject - sample mapping information is available through phs000001.v3.p1.
pht000382
Beschrijving

pht000382

DUMMY ID NUMBER
Beschrijving

ID2

Datatype

string

Alias
UMLS CUI [1,1]
C2348585
STUDY VISIT NUMBER (ALL PARTICIPANTS)
Beschrijving

VISNO

Datatype

text

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C3274381
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
OCULAR PAIN SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

OCPAIN

Datatype

float

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C1299003
UMLS CUI [1,3]
C0449820
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
NEAR ACTIVITIES SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

NEARACT

Datatype

float

Alias
UMLS CUI [1,1]
C0429541
UMLS CUI [1,2]
C0449820
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
DISTANCE ACTIVITIES SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

DISTACT

Datatype

float

Alias
UMLS CUI [1,1]
C0442747
UMLS CUI [1,2]
C0449820
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
VISION SPECIFIC: SOCIAL FUNCTIONING SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

VSOCFUNC

Datatype

float

Alias
UMLS CUI [1,1]
C0042789
UMLS CUI [1,2]
C0679005
UMLS CUI [1,3]
C0449820
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
VISION SPECIFIC: MENTAL HEALTH SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

VMENTALH

Datatype

float

Alias
UMLS CUI [1,1]
C0042789
UMLS CUI [1,2]
C0025353
UMLS CUI [1,3]
C0449820
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
VISION SPECIFIC: ROLE DIFFICULITIES SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

VROLEDIF

Datatype

float

Alias
UMLS CUI [1,1]
C0042789
UMLS CUI [1,2]
C2348235
UMLS CUI [1,3]
C0035820
UMLS CUI [1,4]
C0332218
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
VISION SPECIFIC: DEPENDENCY SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

VDEP

Datatype

float

Alias
UMLS CUI [1,1]
C0042789
UMLS CUI [1,2]
C2348235
UMLS CUI [1,3]
C0011546
UMLS CUI [1,4]
C0439849
UMLS CUI [1,5]
C0449820
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
DRIVING SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

DRIVE

Datatype

float

Alias
UMLS CUI [1,1]
C0004379
UMLS CUI [1,2]
C0449820
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
GENERAL HEALTH SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

GENH

Datatype

float

Alias
UMLS CUI [1,1]
C0516984
UMLS CUI [1,2]
C0449820
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
GENERAL VISION SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

GENVIS

Datatype

float

Alias
UMLS CUI [1,1]
C0205246
UMLS CUI [1,2]
C0042789
UMLS CUI [1,3]
C0449820
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
COLOR VISION SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

COLORV

Datatype

float

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C1880121
UMLS CUI [1,3]
C0449820
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
PERIPHERAL VISION SUBSCALE SCORE (ALL PARTICIPANTS)
Beschrijving

PERIPHV

Datatype

float

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C0205100
UMLS CUI [1,3]
C0042789
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
VFQ OVERALL SCORE (ALL PARTICIPANTS)
Beschrijving

AVTOT

Datatype

float

Alias
UMLS CUI [1,1]
C0200149
UMLS CUI [1,2]
C2964552
UMLS CUI [1,3]
C0042812
UMLS CUI [1,4]
C0034394
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
YEARS FROM RANDOMIZATION TO DATE OF VFQ (ALL PARTICIPANTS)
Beschrijving

VFQTIME

Datatype

float

Maateenheden
  • years
Alias
UMLS CUI [1,1]
C0439234
UMLS CUI [1,2]
C0034656
UMLS CUI [1,3]
C0042812
UMLS CUI [1,4]
C0034394
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C0444868
years
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Similar models

The data table (n=16 variables) contains information about AREDS participants' general vision status (e.g. general vision score, ocular pain score, VFQ overall score), and its effect on participants' behavior (e.g. near and distant activities, social activities, driving, mental health score) as obtained through the VFQ-25 questionnaire. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.

19 Formulieren
  1. StudyEvent: NEI Age-Related Eye Disease Study (AREDS)
    1. Eligibility Criteria
    2. The data table (n=142 variables) contains AMD and cataract phenotype information, medical history and socio-demographic information drawn from several data sets (e.g. enrollment_randomization, amdlensphenotype, followup), plus a unique patient identifier (ID2) for participants with a genetic specimen (to be found only in GENSPECPHENOTYPE and GENSPECFUNDUSLENS [pht000376] tables). Nuclear, cortical and posterior subcapsular opacity information is included for both eyes at baseline and end of study. Other disease information (e.g. diabetes, cancer, angina), medical information (e.g. BMI, blood pressure) and smoking status are also included annually throughout follow-up.
    3. The data table (n=12 variables) contains information about the occurrence of adverse events during the AREDS clinical trial, e.g. type of adverse event, severity, primary ICD9 code, outcome, potential relationship to study drug, timing, and treatment. Data were collected through the clinical trial and for the first 6 months of the natural history follow-up immediately after the clinical trial concluded. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    4. The data table (n=25 variables) contains detailed information about cataract phenotypes (n=23 variables) as well as final AMD phenotype (n=1 variable), and patient ID. Nuclear, cortical and posterior subcapsular opacity information is included for both eyes at baseline and end of study. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    5. The data table (n=56 variables) contains information about AREDS participants' dietary intake of alcohol, amino acids, carbohydrates, fiber, poly- and monounsaturated fatty acids, proteins, vitamins and minerals. Participants' glycemic index and glycemic load are also included. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    6. The data table (n=102 variables) contains AREDS treatment assignment, basic socio-demographic characteristics and baseline medical history for AREDS participants. Medical history information includes eye disease information such as AMD Category, visual acuity, and past ophthalmic treatments (e.g. cataract surgery, laser treatment), as well as information about the presence/absence of other diseases (e.g. angina, arthritis, cancer, diabetes, high blood pressure), use of prescribed drugs for disease management (e.g. blood-thinning medications, digoxin, thyroid hormones, insulin), use of over-the-counter drugs (e.g. NSAIDs, antacids), intake of vitamins and minerals, and smoking history. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    7. The data table (n=83 variables) contains information obtained at follow-up visits during the AREDS clinical trial (every six months following randomization), annually in person during the natural history follow-up, and via phone between annual in-person visits. Variables include information about AREDS participants' ophthalmic medical history (e.g. cataract or other eye surgery, laser treatment for AMD, retinal repair, capsulotomy, presence/absence of lens, glaucoma, and visual acuity) and general medical information, including new diagnoses of cancer, heart disease, stroke, and peripheral vascular disease, disease history of angina and high blood pressure, current disease status of diabetes, arthritis, and gout, use of prescribed drugs for disease treatment or management (e.g. blood-thinning medications, digoxin, thyroid hormones, insulin), use of over-the-counter drugs (e.g. NSAIDs, antacids), and smoking behavior. For version 3 release of the study, visual acuity data of the right eye have been added for odd-numbered visits. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    8. The data table (n=49 variables) contains information from AREDS participants' fundus photographs, including presence, type, and extent of drusen, presence/extent of RPE depigmentation, SSR (serous sensory retinal) detachments, subretinal hemorrhages, subretinal fibrosis, and geographic atrophy. In addition, information on photocoagulation (PC) treatment for AMD SRNV is included, as well as AMD Severity Scale Scores and AMD Simple Scale Scores calculated from the fundus data. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    9. The data table (n=62) contains information only for AREDS participants who have a genetic specimen. A unique patient identifier (ID2 field) for these participants (to be found only in GENSPECPHENOTYPE [pht000001.v2.p1] and GENSPECFUNDUSLENS data tables) is included instead of the patient identifier used for data tables with all participants (ID field). Information about fundus and lens characteristics are included as follows - fundus: presence, type, and extent of drusen, presence/extent of RPE depigmentation, SSR (serous sensory retinal) detachments, subretinal hemorrhages, subretinal fibrosis, and geographic atrophy; lens: degree of nuclear sclerosis, cortical and posterior subcapsular opacities, and iris pigmentation. In addition, information on photocoagulation (PC) treatment for AMD is included as well as AMD Severity Scale Scores and AMD Simple Scale Scores calculated from the fundus data.
    10. The data table (n=6 variables) contains information about AREDS participant hospitalizations (e.g. reason, time from randomization, duration, primary ICD9 code) during the entire study. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    11. The data table (n=21 variables) contains information from AREDS participants' lens photographs, including degree of nuclear sclerosis, cortical and posterior subcapsular opacities, and iris pigmentation. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    12. The data table (n=7 variables) contains information about AREDS participant deaths (e.g. cause, time from randomization) during the entire study. A search using the National Death Index (NDI) yielded additional deaths not identified during the study. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    13. The data table (n=44 variables) contains information about AREDS participants' use (e.g. type, frequency, dose, duration) of non-steroidal anti-inflammatory drugs (e.g. aspirin, ibuprofen, acetaminophen, naproxen). Data were collected at in-clinic visits starting in October 2004. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    14. The data table (n=16 variables) contains information about AREDS participants' general vision status (e.g. general vision score, ocular pain score, VFQ overall score), and its effect on participants' behavior (e.g. near and distant activities, social activities, driving, mental health score) as obtained through the VFQ-25 questionnaire. Note: In version 3, the ID has been replaced by ID2 identifier for all subjects.
    15. Subject - Consent Information
    16. Subject - Sample Mapping (including mapping to Coriell IDs)
    17. The data table (n=2 variables) contains information on subjects' annual exposure to sunlight (hours; April through September).
    18. This dataset provides refractive error values obtained from control subjects of the AREDS study (phs000001.v3.p1) and represents a substudy of AREDS ; data of n=7 new variables are provided in addition to basic sociodemographic data. Subject - consent and subject - sample mapping information is available through phs000001.v3.p1.
    19. This dataset provides refractive error values obtained from control subjects of the AREDS study (phs000001.v3.p1) and represents a substudy of AREDS ; data of n=7 new variables are provided in addition to basic sociodemographic data. Subject - consent and subject - sample mapping information is available through phs000001.v3.p1.
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
pht000382
ID2
Item
DUMMY ID NUMBER
string
C2348585 (UMLS CUI [1,1])
Item
STUDY VISIT NUMBER (ALL PARTICIPANTS)
text
C0545082 (UMLS CUI [1,1])
C3274381 (UMLS CUI [1,2])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
VISNO
Code List
STUDY VISIT NUMBER (ALL PARTICIPANTS)
CL Item
Baseline visit (00)
C1442488 (UMLS CUI [1,1])
C0545082 (UMLS CUI [1,2])
CL Item
0.5-year (01)
C0444500 (UMLS CUI [1,1])
C0439234 (UMLS CUI [1,2])
CL Item
1-year (02)
C0205447 (UMLS CUI [1,1])
C0439234 (UMLS CUI [1,2])
CL Item
1.5-years (03)
C0439234 (UMLS CUI [1,1])
CL Item
2-years (04)
C0205448 (UMLS CUI [1,1])
C0439234 (UMLS CUI [1,2])
CL Item
2.5-years (05)
C3844011 (UMLS CUI [1,1])
C0439234 (UMLS CUI [1,2])
CL Item
3-years (06)
C0439234 (UMLS CUI [1,1])
C0205437 (UMLS CUI [1,2])
CL Item
3.5-years (07)
C0439234 (UMLS CUI [1,1])
CL Item
4-years (08)
C0205450 (UMLS CUI [1,1])
C0439234 (UMLS CUI [1,2])
CL Item
4.5-years (09)
C0439234 (UMLS CUI [1,1])
CL Item
5-years (10)
C0205451 (UMLS CUI [1,1])
C0439234 (UMLS CUI [1,2])
CL Item
5.5-years (11)
C0439234 (UMLS CUI [1,1])
CL Item
6-years (12)
C0205452 (UMLS CUI [1,1])
C0439234 (UMLS CUI [1,2])
CL Item
6.5-years (13)
C0439234 (UMLS CUI [1,1])
CL Item
7-years (14)
C0205453 (UMLS CUI [1,1])
C0439234 (UMLS CUI [1,2])
CL Item
7.5-years (15)
C0439234 (UMLS CUI [1,1])
CL Item
8-years (16)
C0205454 (UMLS CUI [1,1])
C0439234 (UMLS CUI [1,2])
CL Item
8.5-years (17)
C0439234 (UMLS CUI [1,1])
CL Item
9-years (18)
C0439234 (UMLS CUI [1,1])
CL Item
9.5-years (19)
C0439234 (UMLS CUI [1,1])
CL Item
10-years (20)
C0439234 (UMLS CUI [1,1])
CL Item
10.5-years (21)
C0439234 (UMLS CUI [1,1])
CL Item
11-years (22)
C0439234 (UMLS CUI [1,1])
CL Item
11.5-years (23)
C0439234 (UMLS CUI [1,1])
CL Item
12-years (24)
C0439234 (UMLS CUI [1,1])
CL Item
12.5-years (25)
C0439234 (UMLS CUI [1,1])
CL Item
13-years (26)
C0439234 (UMLS CUI [1,1])
OCPAIN
Item
OCULAR PAIN SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0030193 (UMLS CUI [1,1])
C1299003 (UMLS CUI [1,2])
C0449820 (UMLS CUI [1,3])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
NEARACT
Item
NEAR ACTIVITIES SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0429541 (UMLS CUI [1,1])
C0449820 (UMLS CUI [1,2])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
DISTACT
Item
DISTANCE ACTIVITIES SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0442747 (UMLS CUI [1,1])
C0449820 (UMLS CUI [1,2])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
VSOCFUNC
Item
VISION SPECIFIC: SOCIAL FUNCTIONING SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0042789 (UMLS CUI [1,1])
C0679005 (UMLS CUI [1,2])
C0449820 (UMLS CUI [1,3])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
VMENTALH
Item
VISION SPECIFIC: MENTAL HEALTH SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0042789 (UMLS CUI [1,1])
C0025353 (UMLS CUI [1,2])
C0449820 (UMLS CUI [1,3])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
VROLEDIF
Item
VISION SPECIFIC: ROLE DIFFICULITIES SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0042789 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
C0035820 (UMLS CUI [1,3])
C0332218 (UMLS CUI [1,4])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
VDEP
Item
VISION SPECIFIC: DEPENDENCY SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0042789 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
C0011546 (UMLS CUI [1,3])
C0439849 (UMLS CUI [1,4])
C0449820 (UMLS CUI [1,5])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
DRIVE
Item
DRIVING SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0004379 (UMLS CUI [1,1])
C0449820 (UMLS CUI [1,2])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
GENH
Item
GENERAL HEALTH SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0516984 (UMLS CUI [1,1])
C0449820 (UMLS CUI [1,2])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
GENVIS
Item
GENERAL VISION SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0205246 (UMLS CUI [1,1])
C0042789 (UMLS CUI [1,2])
C0449820 (UMLS CUI [1,3])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
COLORV
Item
COLOR VISION SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0200149 (UMLS CUI [1,1])
C1880121 (UMLS CUI [1,2])
C0449820 (UMLS CUI [1,3])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
PERIPHV
Item
PERIPHERAL VISION SUBSCALE SCORE (ALL PARTICIPANTS)
float
C0200149 (UMLS CUI [1,1])
C0205100 (UMLS CUI [1,2])
C0042789 (UMLS CUI [1,3])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
AVTOT
Item
VFQ OVERALL SCORE (ALL PARTICIPANTS)
float
C0200149 (UMLS CUI [1,1])
C2964552 (UMLS CUI [1,2])
C0042812 (UMLS CUI [1,3])
C0034394 (UMLS CUI [1,4])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
VFQTIME
Item
YEARS FROM RANDOMIZATION TO DATE OF VFQ (ALL PARTICIPANTS)
float
C0439234 (UMLS CUI [1,1])
C0034656 (UMLS CUI [1,2])
C0042812 (UMLS CUI [1,3])
C0034394 (UMLS CUI [1,4])
C0681850 (UMLS CUI [2,1])
C0444868 (UMLS CUI [2,2])
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