ID

19916

Description

HEARTS: Heart, Exercise, and Resistance Training Study; ODM derived from: https://clinicaltrials.gov/show/NCT00094250

Lien

https://clinicaltrials.gov/show/NCT00094250

Mots-clés

Versions (1)
  1. 30/01/2017 30/01/2017 -
Téléchargé le

30 janvier 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Cardiovascular Diseases NCT00094250

Anglais

Eligibility Cardiovascular Diseases NCT00094250

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
class ii and iii chf that has been clinically stable for at least 6 months
Description

Congestive heart failure Stable Clinical TNM clinical staging

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C0205360
UMLS CUI [1,3]
C0205210
UMLS CUI [1,4]
C3258246
systolic ejection fraction (lvef) between 20% and 40%
Description

Cardiac ejection fraction Systolic | Left ventricular ejection fraction

Type de données

boolean

Alias
UMLS CUI [1,1]
C0232174
UMLS CUI [1,2]
C0039155
UMLS CUI [2]
C0428772
under the care of a cardiologist who is willing to have the patient participate in the study and who will continue to follow the patient medically during his/her participation
Description

Study Subject Participation Status | patient care Cardiologist

Type de données

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0017313
UMLS CUI [2,2]
C0175906
willing and able to undergo the screening procedures and the 1 month observation period to determine eligibility
Description

Screening procedure Willing | Observation Period Willing

Type de données

boolean

Alias
UMLS CUI [1,1]
C0220908
UMLS CUI [1,2]
C0600109
UMLS CUI [2,1]
C1964257
UMLS CUI [2,2]
C1948053
UMLS CUI [2,3]
C0600109
willing and able to come to the research center three times a week for 4 months to participate in an exercise program consisting of either aerobic exercise only, or aerobic exercise plus resistance training
Description

Participates in exercise program | Exercise, Aerobic | Resistance Training

Type de données

boolean

Alias
UMLS CUI [1]
C1820394
UMLS CUI [2]
C0001701
UMLS CUI [3]
C0872279
able to speak and read english
Description

Able to speak English Language | Able to read English Language

Type de données

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0586740
UMLS CUI [2,2]
C0376245
willing to participate in the study after having the study explained to him/her and has signed an informed consent form
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
eligible for a cardiac rehabilitation program under medicare rules due to a recent acute event
Description

Cardiac event Recent | Patient eligible Cardiac rehabilitation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0741923
UMLS CUI [1,2]
C0332185
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C1548635
UMLS CUI [2,3]
C0700431
any medical condition that would make either exercise unsafe or uncomfortable, such as symptomatic copd, severe arthritis, severe peripheral vascular disease, unstable heart disease, uncontrolled blood pressure, or neurological conditions
Description

Medical condition Exercise Unsafe | Chronic Obstructive Airway Disease Symptomatic | Arthritis Severe | Peripheral Vascular Disease Severe | Heart Disease Unstable | Blood Pressure Uncontrolled | nervous system disorder

Type de données

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0015259
UMLS CUI [1,3]
C4036038
UMLS CUI [2,1]
C0024117
UMLS CUI [2,2]
C0231220
UMLS CUI [3,1]
C0003864
UMLS CUI [3,2]
C0205082
UMLS CUI [4,1]
C0085096
UMLS CUI [4,2]
C0205082
UMLS CUI [5,1]
C0018799
UMLS CUI [5,2]
C0443343
UMLS CUI [6,1]
C0005823
UMLS CUI [6,2]
C0205318
UMLS CUI [7]
C0027765
other complicating diseases, such as severe anemia or other blood dyscrasia affecting function, chronic renal failure, progressive cancer, or unstable diabetes
Description

Disease Complicating | Anemia, severe | Hematological Disease | Kidney Failure, Chronic | Progressive Neoplastic Disease | Brittle diabetes

Type de données

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C1522701
UMLS CUI [2]
C0238644
UMLS CUI [3]
C0018939
UMLS CUI [4]
C0022661
UMLS CUI [5]
C0677932
UMLS CUI [6]
C0342302
does not otherwise meet the above inclusion criteria
Description

Inclusion criteria failed

Type de données

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0231175
Retour au début de la page

Similar models

Eligibility Cardiovascular Diseases NCT00094250

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Congestive heart failure Stable Clinical TNM clinical staging
Item
class ii and iii chf that has been clinically stable for at least 6 months
boolean
C0018802 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0205210 (UMLS CUI [1,3])
C3258246 (UMLS CUI [1,4])
Cardiac ejection fraction Systolic | Left ventricular ejection fraction
Item
systolic ejection fraction (lvef) between 20% and 40%
boolean
C0232174 (UMLS CUI [1,1])
C0039155 (UMLS CUI [1,2])
C0428772 (UMLS CUI [2])
Study Subject Participation Status | patient care Cardiologist
Item
under the care of a cardiologist who is willing to have the patient participate in the study and who will continue to follow the patient medically during his/her participation
boolean
C2348568 (UMLS CUI [1])
C0017313 (UMLS CUI [2,1])
C0175906 (UMLS CUI [2,2])
Screening procedure Willing | Observation Period Willing
Item
willing and able to undergo the screening procedures and the 1 month observation period to determine eligibility
boolean
C0220908 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
C1964257 (UMLS CUI [2,1])
C1948053 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Participates in exercise program | Exercise, Aerobic | Resistance Training
Item
willing and able to come to the research center three times a week for 4 months to participate in an exercise program consisting of either aerobic exercise only, or aerobic exercise plus resistance training
boolean
C1820394 (UMLS CUI [1])
C0001701 (UMLS CUI [2])
C0872279 (UMLS CUI [3])
Able to speak English Language | Able to read English Language
Item
able to speak and read english
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0586740 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
Informed Consent
Item
willing to participate in the study after having the study explained to him/her and has signed an informed consent form
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Cardiac event Recent | Patient eligible Cardiac rehabilitation
Item
eligible for a cardiac rehabilitation program under medicare rules due to a recent acute event
boolean
C0741923 (UMLS CUI [1,1])
C0332185 (UMLS CUI [1,2])
C0030705 (UMLS CUI [2,1])
C1548635 (UMLS CUI [2,2])
C0700431 (UMLS CUI [2,3])
Medical condition Exercise Unsafe | Chronic Obstructive Airway Disease Symptomatic | Arthritis Severe | Peripheral Vascular Disease Severe | Heart Disease Unstable | Blood Pressure Uncontrolled | nervous system disorder
Item
any medical condition that would make either exercise unsafe or uncomfortable, such as symptomatic copd, severe arthritis, severe peripheral vascular disease, unstable heart disease, uncontrolled blood pressure, or neurological conditions
boolean
C3843040 (UMLS CUI [1,1])
C0015259 (UMLS CUI [1,2])
C4036038 (UMLS CUI [1,3])
C0024117 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
C0003864 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0085096 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0018799 (UMLS CUI [5,1])
C0443343 (UMLS CUI [5,2])
C0005823 (UMLS CUI [6,1])
C0205318 (UMLS CUI [6,2])
C0027765 (UMLS CUI [7])
Disease Complicating | Anemia, severe | Hematological Disease | Kidney Failure, Chronic | Progressive Neoplastic Disease | Brittle diabetes
Item
other complicating diseases, such as severe anemia or other blood dyscrasia affecting function, chronic renal failure, progressive cancer, or unstable diabetes
boolean
C0012634 (UMLS CUI [1,1])
C1522701 (UMLS CUI [1,2])
C0238644 (UMLS CUI [2])
C0018939 (UMLS CUI [3])
C0022661 (UMLS CUI [4])
C0677932 (UMLS CUI [5])
C0342302 (UMLS CUI [6])
Inclusion criteria failed
Item
does not otherwise meet the above inclusion criteria
boolean
C1512693 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
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