Informatie:
Fout:
ID
44725
Beschrijving
Effect of Combined Exercise Post-treatment Intervention in Lean Mass Recovery in Breast Cancer Survival.; ODM derived from: https://clinicaltrials.gov/show/NCT01843608
Link
https://clinicaltrials.gov/show/NCT01843608
Trefwoorden
Versies (1)
- 28-09-21 28-09-21 -
Houder van rechten
Universidad Politecnica de Madrid
Geüploaded op
28 september 2021
DOI
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Licentie
Creative Commons BY-NC 4.0
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Eligibility Sarcopenic Obesity in Breast Cancer Survival NCT01843608
Eligibility Sarcopenic Obesity in Breast Cancer Survival NCT01843608
- StudyEvent: Eligibility
Similar models
Eligibility Sarcopenic Obesity in Breast Cancer Survival NCT01843608
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Breast Carcinoma, TNM clinical staging
Item
breast cancer diagnosed confirmed stage i-iiia.
boolean
C0678222 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,2])
Randomized disposition
Item
randomized disposition.
boolean
C0034656 (UMLS CUI [1,1])
C0743223 (UMLS CUI [1,2])
C0743223 (UMLS CUI [1,2])
Duration after finishing treatments
Item
minimum of forty-five days and maximum of thirty-six months after finishing treatments (chemotherapy and radiotherapy).
boolean
C0087111 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
C0205197 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
ECOG performance status
Item
0-1 in eastern cooperative oncology group (ecog) scale (present the ability to walk briskly)
boolean
C1520224 (UMLS CUI [1])
Oncologist approval
Item
oncologist approval.
boolean
C2346845 (UMLS CUI [1,1])
C0259990 (UMLS CUI [1,2])
C0259990 (UMLS CUI [1,2])
Informed consent
Item
informed consent signed.
boolean
C0021430 (UMLS CUI [1])
City of residence
Item
community of madrid inhabitant.
boolean
C2316883 (UMLS CUI [1])
Neoplasm Metastasis
Item
metastasis presence
boolean
C0027627 (UMLS CUI [1])
Serious comorbidity | Unstable cardiac condition | Severe pulmonary disease | Anticoagulants treatments.
Item
serious medical risk such as unstable cardiac condition or severe pulmonary disease and anticoagulants treatments.
boolean
C0009488 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0007222 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
C0024115 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0003280 (UMLS CUI [4])
C0205404 (UMLS CUI [1,2])
C0007222 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
C0024115 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0003280 (UMLS CUI [4])
Oncology or primary care approval who verified the medical risk exclusion criteria
Item
oncology or primary care approval who verified the medical risk exclusion criteria.
boolean
C0680251 (UMLS CUI [1,1])
C0259990 (UMLS CUI [1,2])
C0680251 (UMLS CUI [2,1])
C2735026 (UMLS CUI [2,2])
C0259990 (UMLS CUI [1,2])
C0680251 (UMLS CUI [2,1])
C2735026 (UMLS CUI [2,2])
ECOG performance status
Item
ecog > 1
boolean
C1520224 (UMLS CUI [1])
Pregnancy
Item
pregnant
boolean
C0032961 (UMLS CUI [1])