ID

31415

Beskrivning

Study of Tai Chi Exercise and Balance in Persons With Parkinson's Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00611481

Länk

https://clinicaltrials.gov/show/NCT00611481

Nyckelord

Versioner (1)
  1. 2018-08-20 2018-08-20 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

20 augusti 2018

DOI

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Licens

Creative Commons BY 4.0
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Eligibility Parkinson's Disease NCT00611481

Engelsk

Eligibility Parkinson's Disease NCT00611481

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients who have:
Beskrivning

Patients Have

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C3539897
a diagnosis of idiopathic pd, with a disease severity rating of stage i to iv on the hoehn and yahr scale (hoehn & yahr, 1967)
Beskrivning

Parkinson Disease Hoehn and Yahr Scale

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0030567
UMLS CUI [1,2]
C4274667
at least 1 score of 2 or more for at least 1 limb for either the tremor, rigidity, or bradykinesia item of the unified parkinson's disease rating scale (updrs)
Beskrivning

Limb Quantity Tremor UPDRS | Limb Quantity Muscle Rigidity UPDRS | Limb Quantity Bradykinesia UPDRS

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0015385
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0040822
UMLS CUI [1,4]
C3639721
UMLS CUI [2,1]
C0015385
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0026837
UMLS CUI [2,4]
C3639721
UMLS CUI [3,1]
C0015385
UMLS CUI [3,2]
C1265611
UMLS CUI [3,3]
C0233565
UMLS CUI [3,4]
C3639721
stable medication usage
Beskrivning

Pharmaceutical Preparations Usage Stable

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0457083
UMLS CUI [1,3]
C0205360
not participated in a structured exercise program (i.e., not involved in any routine, organized physical activity program lasting 30 minutes or more per day, such as a gym program or regularly scheduled instructor-led exercise class) in the previous 2 months
Beskrivning

Absence Participation Exercise Program

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C0015259
UMLS CUI [1,4]
C3484370
ability to stand unaided or walk independently; had a personal physician's or neurologist's clearance for participation; and had a willingness to be assigned to intervention conditions.
Beskrivning

Able to stand alone | Able to walk Independent | Study Subject Participation Status Approved | Interventional procedure Willing

Datatyp

boolean

Alias
UMLS CUI [1]
C0560202
UMLS CUI [2,1]
C2712089
UMLS CUI [2,2]
C1299583
UMLS CUI [3,1]
C2348568
UMLS CUI [3,2]
C0205540
UMLS CUI [4,1]
C0184661
UMLS CUI [4,2]
C0600109
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who:
Beskrivning

Patients Have

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C3539897
participate in any other behavioral or pharmacological research study
Beskrivning

Study Subject Participation Status | Behavioral Research | Research pharmacological

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0004939
UMLS CUI [3,1]
C0035168
UMLS CUI [3,2]
C0205464
have cognitive decline (mini-mental state examination score, ≤ 24) (folstein et al., 1975)
Beskrivning

Impaired cognition Mini-mental state examination

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0338656
UMLS CUI [1,2]
C0451306
have self-reported diagnosis of alzheimer disease or other severe neurological (stage iii and iv pd)
Beskrivning

Alzheimer's Disease | Nervous system disorder Severe | Parkinson Disease Hoehn and Yahr Stage

Datatyp

boolean

Alias
UMLS CUI [1]
C0002395
UMLS CUI [2,1]
C0027765
UMLS CUI [2,2]
C0205082
UMLS CUI [3,1]
C0030567
UMLS CUI [3,2]
C3639483
have evidence of progressive or debilitating conditions (metastatic cancer, severe heart or lung disease, crippling arthritis) or severe losses in vision and hearing that would limit their tolerance to testing and training procedures, that would interfere with study participation
Beskrivning

Progressive Disease | Debilitation | Neoplasm Metastasis | Heart Disease Severe | Lung disease Severe | Arthritis crippling | Severe loss of vision | Severe hearing loss | Testing Limited | Training Limited | Interference Study Subject Participation Status

Datatyp

boolean

Alias
UMLS CUI [1]
C1335499
UMLS CUI [2]
C0742985
UMLS CUI [3]
C0027627
UMLS CUI [4,1]
C0018799
UMLS CUI [4,2]
C0205082
UMLS CUI [5,1]
C0024115
UMLS CUI [5,2]
C0205082
UMLS CUI [6,1]
C0003864
UMLS CUI [6,2]
C0010331
UMLS CUI [7]
C3552074
UMLS CUI [8]
C3874334
UMLS CUI [9,1]
C0039593
UMLS CUI [9,2]
C0439801
UMLS CUI [10,1]
C2673163
UMLS CUI [10,2]
C0439801
UMLS CUI [11,1]
C0521102
UMLS CUI [11,2]
C2348568
are unavailable during the study period.
Beskrivning

Patients Unavailable

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0686905
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Similar models

Eligibility Parkinson's Disease NCT00611481

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Patients Have
Item
patients who have:
boolean
C0030705 (UMLS CUI [1,1])
C3539897 (UMLS CUI [1,2])
Parkinson Disease Hoehn and Yahr Scale
Item
a diagnosis of idiopathic pd, with a disease severity rating of stage i to iv on the hoehn and yahr scale (hoehn & yahr, 1967)
boolean
C0030567 (UMLS CUI [1,1])
C4274667 (UMLS CUI [1,2])
Limb Quantity Tremor UPDRS | Limb Quantity Muscle Rigidity UPDRS | Limb Quantity Bradykinesia UPDRS
Item
at least 1 score of 2 or more for at least 1 limb for either the tremor, rigidity, or bradykinesia item of the unified parkinson's disease rating scale (updrs)
boolean
C0015385 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0040822 (UMLS CUI [1,3])
C3639721 (UMLS CUI [1,4])
C0015385 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0026837 (UMLS CUI [2,3])
C3639721 (UMLS CUI [2,4])
C0015385 (UMLS CUI [3,1])
C1265611 (UMLS CUI [3,2])
C0233565 (UMLS CUI [3,3])
C3639721 (UMLS CUI [3,4])
Pharmaceutical Preparations Usage Stable
Item
stable medication usage
boolean
C0013227 (UMLS CUI [1,1])
C0457083 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
Absence Participation Exercise Program
Item
not participated in a structured exercise program (i.e., not involved in any routine, organized physical activity program lasting 30 minutes or more per day, such as a gym program or regularly scheduled instructor-led exercise class) in the previous 2 months
boolean
C0332197 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
C3484370 (UMLS CUI [1,4])
Able to stand alone | Able to walk Independent | Study Subject Participation Status Approved | Interventional procedure Willing
Item
ability to stand unaided or walk independently; had a personal physician's or neurologist's clearance for participation; and had a willingness to be assigned to intervention conditions.
boolean
C0560202 (UMLS CUI [1])
C2712089 (UMLS CUI [2,1])
C1299583 (UMLS CUI [2,2])
C2348568 (UMLS CUI [3,1])
C0205540 (UMLS CUI [3,2])
C0184661 (UMLS CUI [4,1])
C0600109 (UMLS CUI [4,2])
Item Group
C0680251 (UMLS CUI)
Patients Have
Item
patients who:
boolean
C0030705 (UMLS CUI [1,1])
C3539897 (UMLS CUI [1,2])
Study Subject Participation Status | Behavioral Research | Research pharmacological
Item
participate in any other behavioral or pharmacological research study
boolean
C2348568 (UMLS CUI [1])
C0004939 (UMLS CUI [2])
C0035168 (UMLS CUI [3,1])
C0205464 (UMLS CUI [3,2])
Impaired cognition Mini-mental state examination
Item
have cognitive decline (mini-mental state examination score, ≤ 24) (folstein et al., 1975)
boolean
C0338656 (UMLS CUI [1,1])
C0451306 (UMLS CUI [1,2])
Alzheimer's Disease | Nervous system disorder Severe | Parkinson Disease Hoehn and Yahr Stage
Item
have self-reported diagnosis of alzheimer disease or other severe neurological (stage iii and iv pd)
boolean
C0002395 (UMLS CUI [1])
C0027765 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0030567 (UMLS CUI [3,1])
C3639483 (UMLS CUI [3,2])
Progressive Disease | Debilitation | Neoplasm Metastasis | Heart Disease Severe | Lung disease Severe | Arthritis crippling | Severe loss of vision | Severe hearing loss | Testing Limited | Training Limited | Interference Study Subject Participation Status
Item
have evidence of progressive or debilitating conditions (metastatic cancer, severe heart or lung disease, crippling arthritis) or severe losses in vision and hearing that would limit their tolerance to testing and training procedures, that would interfere with study participation
boolean
C1335499 (UMLS CUI [1])
C0742985 (UMLS CUI [2])
C0027627 (UMLS CUI [3])
C0018799 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0024115 (UMLS CUI [5,1])
C0205082 (UMLS CUI [5,2])
C0003864 (UMLS CUI [6,1])
C0010331 (UMLS CUI [6,2])
C3552074 (UMLS CUI [7])
C3874334 (UMLS CUI [8])
C0039593 (UMLS CUI [9,1])
C0439801 (UMLS CUI [9,2])
C2673163 (UMLS CUI [10,1])
C0439801 (UMLS CUI [10,2])
C0521102 (UMLS CUI [11,1])
C2348568 (UMLS CUI [11,2])
Patients Unavailable
Item
are unavailable during the study period.
boolean
C0030705 (UMLS CUI [1,1])
C0686905 (UMLS CUI [1,2])
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