ID

43565

Description

Hypnosis in Treating Hot Flashes in Breast Cancer Survivors; ODM derived from: https://clinicaltrials.gov/show/NCT00094133

Lien

https://clinicaltrials.gov/show/NCT00094133

Mots-clés

  1. 09/01/2017 09/01/2017 -
  2. 20/09/2021 20/09/2021 -
Téléchargé le

20 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Breast Cancer NCT00094133

Eligibility Breast Cancer NCT00094133

Criteria
Description

Criteria

history of primary breast cancer
Description

Primary malignant neoplasm of breast

Type de données

boolean

Alias
UMLS CUI [1]
C1299258
no evidence of detectable disease
Description

Disease Detectable Evidence

Type de données

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C3830527
UMLS CUI [1,3]
C3887511
at least 14 hot flashes per week for ≥ 1 month by self-reporting
Description

Hot flashes Quantity Weekly

Type de données

boolean

Alias
UMLS CUI [1,1]
C0600142
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0332174
hormone receptor status not specified
Description

Hormone Receptor Status Unspecified

Type de données

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
UMLS CUI [1,3]
C0205370
patient characteristics:
Description

Client Characteristics

Type de données

boolean

Alias
UMLS CUI [1]
C0815172
female
Description

Gender

Type de données

boolean

Alias
UMLS CUI [1]
C0079399
life expectancy > 6 months
Description

Life Expectancy

Type de données

boolean

Alias
UMLS CUI [1]
C0023671
menopausal status not specified
Description

Menopausal Status Unspecified

Type de données

boolean

Alias
UMLS CUI [1,1]
C3829127
UMLS CUI [1,2]
C0205370
outpatient status
Description

Outpatient

Type de données

boolean

Alias
UMLS CUI [1]
C0029921
no medical or psychiatric condition that would preclude study participation
Description

Medical condition Study Subject Participation Status Exclusion | Mental disorder Study Subject Participation Status Exclusion

Type de données

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C2828389
UMLS CUI [2,1]
C0004936
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C2828389
prior concurrent therapy:
Description

Therapeutic procedure

Type de données

boolean

Alias
UMLS CUI [1]
C0087111
concurrent antihormonal agents for breast cancer (e.g., tamoxifen or raloxifene) allowed provided the patient has been on them for ≥ 1 month
Description

Hormone Antagonists Breast Carcinoma | Tamoxifen | Raloxifene

Type de données

boolean

Alias
UMLS CUI [1,1]
C0019927
UMLS CUI [1,2]
C0678222
UMLS CUI [2]
C0039286
UMLS CUI [3]
C0244404
no other concurrent hormonal therapy
Description

Hormone Therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0279025
no other putative therapies for hot flashes ≥ 1 month prior to study entry
Description

Therapeutic procedure Suspected Hot flashes

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0750491
UMLS CUI [1,3]
C0600142
concurrent vitamin e allowed
Description

Vitamin E

Type de données

boolean

Alias
UMLS CUI [1]
C0042874
no other concurrent treatment for hot flashes
Description

Therapeutic procedure Hot flashes

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0600142
no concurrent cytotoxic chemotherapy
Description

Cytotoxic Chemotherapy

Type de données

boolean

Alias
UMLS CUI [1]
C0677881
not concurrently using hypnosis for any reason
Description

Hypnosis reason for

Type de données

boolean

Alias
UMLS CUI [1,1]
C3888013
UMLS CUI [1,2]
C0392360

Similar models

Eligibility Breast Cancer NCT00094133

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
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])
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])
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])
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
C3829127 (UMLS CUI [1,1])
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])
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])
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])
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])
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])

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial