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Information:
Fel:
ID
19552
Beskrivning
Hypnosis in Treating Hot Flashes in Breast Cancer Survivors; ODM derived from: https://clinicaltrials.gov/show/NCT00094133
Länk
https://clinicaltrials.gov/show/NCT00094133
Nyckelord
Versioner (2)
- 2017-01-09 2017-01-09 -
- 2021-09-20 2021-09-20 -
Uppladdad den
9 januari 2017
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00094133
Eligibility Breast Cancer NCT00094133
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00094133
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Primary malignant neoplasm of breast
Item
history of primary breast cancer
boolean
C1299258 (UMLS CUI [1])
Disease Detectable Evidence
Item
no evidence of detectable disease
boolean
C0012634 (UMLS CUI [1,1])
C3830527 (UMLS CUI [1,2])
C3887511 (UMLS CUI [1,3])
C3830527 (UMLS CUI [1,2])
C3887511 (UMLS CUI [1,3])
Hot flashes Quantity Weekly
Item
at least 14 hot flashes per week for ≥ 1 month by self-reporting
boolean
C0600142 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0332174 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,2])
C0332174 (UMLS CUI [1,3])
Hormone Receptor Status Unspecified
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Life Expectancy
Item
life expectancy > 6 months
boolean
C0023671 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C1513126 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,2])
Outpatient
Item
outpatient status
boolean
C0029921 (UMLS CUI [1])
Medical condition Study Subject Participation Status Exclusion | Mental disorder Study Subject Participation Status Exclusion
Item
no medical or psychiatric condition that would preclude study participation
boolean
C3843040 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
C0004936 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C2828389 (UMLS CUI [2,3])
C2348568 (UMLS CUI [1,2])
C2828389 (UMLS CUI [1,3])
C0004936 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C2828389 (UMLS CUI [2,3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
Hormone Antagonists Breast Carcinoma | Tamoxifen | Raloxifene
Item
concurrent antihormonal agents for breast cancer (e.g., tamoxifen or raloxifene) allowed provided the patient has been on them for ≥ 1 month
boolean
C0019927 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0039286 (UMLS CUI [2])
C0244404 (UMLS CUI [3])
C0678222 (UMLS CUI [1,2])
C0039286 (UMLS CUI [2])
C0244404 (UMLS CUI [3])
Hormone Therapy
Item
no other concurrent hormonal therapy
boolean
C0279025 (UMLS CUI [1])
Therapeutic procedure Suspected Hot flashes
Item
no other putative therapies for hot flashes ≥ 1 month prior to study entry
boolean
C0087111 (UMLS CUI [1,1])
C0750491 (UMLS CUI [1,2])
C0600142 (UMLS CUI [1,3])
C0750491 (UMLS CUI [1,2])
C0600142 (UMLS CUI [1,3])
Vitamin E
Item
concurrent vitamin e allowed
boolean
C0042874 (UMLS CUI [1])
Therapeutic procedure Hot flashes
Item
no other concurrent treatment for hot flashes
boolean
C0087111 (UMLS CUI [1,1])
C0600142 (UMLS CUI [1,2])
C0600142 (UMLS CUI [1,2])
Cytotoxic Chemotherapy
Item
no concurrent cytotoxic chemotherapy
boolean
C0677881 (UMLS CUI [1])
Hypnosis reason for
Item
not concurrently using hypnosis for any reason
boolean
C3888013 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])