ID

12188

Descripción

Staying Positive With Arthritis Study; ODM derived from: https://clinicaltrials.gov/show/NCT02223858

Link

https://clinicaltrials.gov/show/NCT02223858

Palabras clave

Versiones (1)
  1. 12/10/15 12/10/15 -
Subido en

12 de octubre de 2015

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Arthritis NCT02223858

Inglés

Eligibility Arthritis NCT02223858

1 formularios  
  1. StudyEvent: Eligibility
    1. Eligibility Arthritis NCT02223858
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
the target population will be african american (aa) and white (wh) veterans with symptomatic knee arthritis. specific inclusion criteria include:
Descripción

Ethnic group; symptomatic knee arthritis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0015031
UMLS CUI [2,1]
C0231220
UMLS CUI [2,2]
C0240111
age 50 years or older
Descripción

age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
receive primary care at a participating study site
Descripción

study site; primary health care

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2825164
UMLS CUI [2]
C0033137
self-report as non-hispanic black/aa or non-hispanic wh
Descripción

Self-Report; Ethnic group

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2700446
UMLS CUI [2]
C0015031
frequent, symptomatic knee pain identified using questions from the oa initiative
Descripción

symptomatic knee pain

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0231220
UMLS CUI [1,2]
C0231749
pain level of 4 or higher on a 0-10 numeric rating scale
Descripción

pain scale

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1504479
can speak, read, and write in english
Descripción

english

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0376245
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients will be excluded if they:
Descripción

Exclude

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0332196
report serious problems with hearing, eyesight, or memory
Descripción

Abnormal vision; abnormal sensation of hearing; memory impairment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3665386
UMLS CUI [2]
C0848412
UMLS CUI [3]
C0233794
report having been diagnosed any type of arthritis other than osteoarthritis or degenerative arthritis
Descripción

Arthritis; except for degenerative polyarthritis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003864
UMLS CUI [2,1]
C0332300
UMLS CUI [2,2]
C0029408
report that they have been treated for cancer in the last 3 years
Descripción

cancer

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006826
report having had a steroid injection into one or both knees in the past 3 months
Descripción

steroid injection

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1261311
report that there is a reason they cannot complete the study procedures, which include telephone calls and program activities that involve reading and writing
Descripción

Disruption Clinical Research

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0332453
UMLS CUI [1,2]
C0008972
do not have a telephone number where they can receive telephone calls from research staff
Descripción

telephone number

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1515258
screen positive for cognitive impairment
Descripción

Impaired cognition

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0338656
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Similar models

Eligibility Arthritis NCT02223858

1 formularios
  1. StudyEvent: Eligibility
    1. Eligibility Arthritis NCT02223858
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Ethnic group; symptomatic knee arthritis
Item
the target population will be african american (aa) and white (wh) veterans with symptomatic knee arthritis. specific inclusion criteria include:
boolean
C0015031 (UMLS CUI [1])
C0231220 (UMLS CUI [2,1])
C0240111 (UMLS CUI [2,2])
age
Item
age 50 years or older
boolean
C0001779 (UMLS CUI [1])
study site; primary health care
Item
receive primary care at a participating study site
boolean
C2825164 (UMLS CUI [1])
C0033137 (UMLS CUI [2])
Self-Report; Ethnic group
Item
self-report as non-hispanic black/aa or non-hispanic wh
boolean
C2700446 (UMLS CUI [1])
C0015031 (UMLS CUI [2])
symptomatic knee pain
Item
frequent, symptomatic knee pain identified using questions from the oa initiative
boolean
C0231220 (UMLS CUI [1,1])
C0231749 (UMLS CUI [1,2])
pain scale
Item
pain level of 4 or higher on a 0-10 numeric rating scale
boolean
C1504479 (UMLS CUI [1])
english
Item
can speak, read, and write in english
boolean
C0376245 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Exclude
Item
patients will be excluded if they:
boolean
C0332196 (UMLS CUI [1])
Abnormal vision; abnormal sensation of hearing; memory impairment
Item
report serious problems with hearing, eyesight, or memory
boolean
C3665386 (UMLS CUI [1])
C0848412 (UMLS CUI [2])
C0233794 (UMLS CUI [3])
Arthritis; except for degenerative polyarthritis
Item
report having been diagnosed any type of arthritis other than osteoarthritis or degenerative arthritis
boolean
C0003864 (UMLS CUI [1])
C0332300 (UMLS CUI [2,1])
C0029408 (UMLS CUI [2,2])
cancer
Item
report that they have been treated for cancer in the last 3 years
boolean
C0006826 (UMLS CUI [1])
steroid injection
Item
report having had a steroid injection into one or both knees in the past 3 months
boolean
C1261311 (UMLS CUI [1])
Disruption Clinical Research
Item
report that there is a reason they cannot complete the study procedures, which include telephone calls and program activities that involve reading and writing
boolean
C0332453 (UMLS CUI [1,1])
C0008972 (UMLS CUI [1,2])
telephone number
Item
do not have a telephone number where they can receive telephone calls from research staff
boolean
C1515258 (UMLS CUI [1])
Impaired cognition
Item
screen positive for cognitive impairment
boolean
C0338656 (UMLS CUI [1])
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