ID

12645

Beschrijving

Exercise and Quality of Life in Leukemia Patients; ODM derived from: https://clinicaltrials.gov/show/NCT02246907

Link

https://clinicaltrials.gov/show/NCT02246907

Trefwoorden

  1. 07-12-15 07-12-15 -
Geüploaded op

7 december 2015

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Acute Leukemia NCT02246907

Eligibility Acute Leukemia NCT02246907

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
newly diagnosed with acute leukemia by pathology report
Beschrijving

acute leukemia

Datatype

boolean

Alias
UMLS CUI [1]
C0085669
admitted for induction chemotherapy within in the previous 96 hours or +/- 3 days from initiation of induction chemotherapy
Beschrijving

admitted for induction chemotherapy within in the previous 96 hours

Datatype

boolean

Alias
UMLS CUI [1]
C3179010
UMLS CUI [2]
C1320532
an expected hospital stay of 3-4 weeks or longer
Beschrijving

expected hospital stay

Datatype

boolean

Alias
UMLS CUI [1]
C4019085
participation in the study must be approved by the physician directly responsible for the patient's care while at university of north carolina -hospitals
Beschrijving

participation in the study must be approved by the physician directly responsible for the patient's care

Datatype

boolean

Alias
UMLS CUI [1]
C1710470
UMLS CUI [2]
C1706842
age >21 years of age
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
willing and able to provide, signed informed consent
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
willing and able to use a computer to complete study questionnaires
Beschrijving

willing and able to use a computer to complete study questionnaires

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
ability to understand and speak english
Beschrijving

ability to understand and speak english

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
cardiovascular disease (unless the disease would not compromise the patient's ability to participate in the exercise rehabilitation program)
Beschrijving

the criteria below will be determined by the patient's physician and a review of the patient's medical history. if any of the exclusion criteria are observed, the patients will be informed and excluded from participating in the study. participation in this study will involve the same risks as any exercise regimen. given the potential risks involved, patients will be screened for exclusion based upon the following criteria

Datatype

boolean

Alias
UMLS CUI [1]
C0007222
acute or chronic respiratory disease that would compromise the patient's ability to participate in the exercise rehabilitation program
Beschrijving

respiratory disease

Datatype

boolean

Alias
UMLS CUI [1]
C0035204
acute or chronic bone, joint, or muscular abnormalities that would compromise the patient's ability to participate in the exercise rehabilitation program
Beschrijving

acute or chronic bone, joint, or muscular abnormalities that would compromise the patient's ability to participate in the exercise rehabilitation program

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
UMLS CUI [2]
C0439801
UMLS CUI [3]
C0009488
inability to understand and speak english
Beschrijving

inability to understand and speak english

Datatype

boolean

Alias
UMLS CUI [1]
C0237167
dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent
Beschrijving

dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0439801
UMLS CUI [3]
C0009488
another active malignancy
Beschrijving

malignancy

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
patients will also be excluded if they have active bleeding, acute thrombosis, ischemia, hemodynamically unstable, and uncontrolled pain.
Beschrijving

patients will also be excluded if they have active bleeding, acute thrombosis, ischemia, hemodynamically unstable, and uncontrolled pain.

Datatype

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488

Similar models

Eligibility Acute Leukemia NCT02246907

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
acute leukemia
Item
newly diagnosed with acute leukemia by pathology report
boolean
C0085669 (UMLS CUI [1])
admitted for induction chemotherapy within in the previous 96 hours
Item
admitted for induction chemotherapy within in the previous 96 hours or +/- 3 days from initiation of induction chemotherapy
boolean
C3179010 (UMLS CUI [1])
C1320532 (UMLS CUI [2])
expected hospital stay
Item
an expected hospital stay of 3-4 weeks or longer
boolean
C4019085 (UMLS CUI [1])
participation in the study must be approved by the physician directly responsible for the patient's care
Item
participation in the study must be approved by the physician directly responsible for the patient's care while at university of north carolina -hospitals
boolean
C1710470 (UMLS CUI [1])
C1706842 (UMLS CUI [2])
Age
Item
age >21 years of age
boolean
C0001779 (UMLS CUI [1])
informed consent
Item
willing and able to provide, signed informed consent
boolean
C0021430 (UMLS CUI [1])
willing and able to use a computer to complete study questionnaires
Item
willing and able to use a computer to complete study questionnaires
boolean
C1321605 (UMLS CUI [1])
ability to understand and speak english
Item
ability to understand and speak english
boolean
C1321605 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
cardiovascular disease
Item
cardiovascular disease (unless the disease would not compromise the patient's ability to participate in the exercise rehabilitation program)
boolean
C0007222 (UMLS CUI [1])
respiratory disease
Item
acute or chronic respiratory disease that would compromise the patient's ability to participate in the exercise rehabilitation program
boolean
C0035204 (UMLS CUI [1])
acute or chronic bone, joint, or muscular abnormalities that would compromise the patient's ability to participate in the exercise rehabilitation program
Item
acute or chronic bone, joint, or muscular abnormalities that would compromise the patient's ability to participate in the exercise rehabilitation program
boolean
C1321605 (UMLS CUI [1])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])
inability to understand and speak english
Item
inability to understand and speak english
boolean
C0237167 (UMLS CUI [1])
dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent
Item
dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent
boolean
C0021430 (UMLS CUI [1])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])
malignancy
Item
another active malignancy
boolean
C0006826 (UMLS CUI [1])
patients will also be excluded if they have active bleeding, acute thrombosis, ischemia, hemodynamically unstable, and uncontrolled pain.
Item
patients will also be excluded if they have active bleeding, acute thrombosis, ischemia, hemodynamically unstable, and uncontrolled pain.
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])

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