Informações:
Falhas:
ID
35654
Descrição
Omega-3 for Depression and Other Cardiac Risk Factors - 2; ODM derived from: https://clinicaltrials.gov/show/NCT02021669
Link
https://clinicaltrials.gov/show/NCT02021669
Palavras-chave
Versões (1)
- 14/03/2019 14/03/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
14 de março de 2019
DOI
Para um pedido faça login.
Licença
Creative Commons BY 4.0
Comentários do modelo :
Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.
Comentários do grupo de itens para :
Comentários do item para :
Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.
Eligibility Depression NCT02021669
Eligibility Depression NCT02021669
- StudyEvent: Eligibility
Similar models
Eligibility Depression NCT02021669
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Coronary heart disease
Item
documented coronary heart disease
boolean
C0010068 (UMLS CUI [1])
Major Depressive Disorder
Item
diagnosis of major depression based on structured interview
boolean
C1269683 (UMLS CUI [1])
Moderate cognitive impairment | Severe cognitive impairment
Item
moderate to severe cognitive impairment
boolean
C3839816 (UMLS CUI [1])
C3554639 (UMLS CUI [2])
C3554639 (UMLS CUI [2])
Depressive disorder Due to Medical condition General | Depressive disorder Due to Pharmaceutical Preparations
Item
meets dsm-5 criteria for depressive disorder due to a general medical condition or medication
boolean
C0011581 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C3843040 (UMLS CUI [1,3])
C0205246 (UMLS CUI [1,4])
C0011581 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0013227 (UMLS CUI [2,3])
C0678226 (UMLS CUI [1,2])
C3843040 (UMLS CUI [1,3])
C0205246 (UMLS CUI [1,4])
C0011581 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0013227 (UMLS CUI [2,3])
Axis I diagnosis Major | Exception Unipolar Depression | Anxiety Disorders | High suicide risk | Substance Use Disorders | Exception Tobacco Use Disorder
Item
major axis i psychiatric disorder other than unipolar depression or an anxiety disorder, a high risk of suicide, or current substance abuse other than tobacco;
boolean
C0270287 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0041696 (UMLS CUI [2,2])
C0003469 (UMLS CUI [3])
C1271074 (UMLS CUI [4])
C0038586 (UMLS CUI [5])
C1705847 (UMLS CUI [6,1])
C0040336 (UMLS CUI [6,2])
C0205164 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0041696 (UMLS CUI [2,2])
C0003469 (UMLS CUI [3])
C1271074 (UMLS CUI [4])
C0038586 (UMLS CUI [5])
C1705847 (UMLS CUI [6,1])
C0040336 (UMLS CUI [6,2])
Life Expectancy | Intolerance Study Protocol
Item
not expected to survive one year or physically unable to tolerate the study protocol
boolean
C0023671 (UMLS CUI [1])
C0231199 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
C0231199 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
Sertraline allergy | Hypersensitivity Omega-3 Fatty Acids | Fish oils allergy | Shellfish allergy
Item
known sensitivity to sertraline or omega-3, or an allergy to fish oil or shellfish
boolean
C0570766 (UMLS CUI [1])
C0020517 (UMLS CUI [2,1])
C0015689 (UMLS CUI [2,2])
C0571871 (UMLS CUI [3])
C0577625 (UMLS CUI [4])
C0020517 (UMLS CUI [2,1])
C0015689 (UMLS CUI [2,2])
C0571871 (UMLS CUI [3])
C0577625 (UMLS CUI [4])
Antidepressive Agents | Omega-3 Fatty Acids Supplement
Item
taking an antidepressant or an omega-3 supplement at baseline
boolean
C0003289 (UMLS CUI [1])
C0015689 (UMLS CUI [2,1])
C0242295 (UMLS CUI [2,2])
C0015689 (UMLS CUI [2,1])
C0242295 (UMLS CUI [2,2])
Exemption Cardiologist | Exemption Primary Care Physician
Item
exempted by their cardiologist or primary care physician
boolean
C2348482 (UMLS CUI [1,1])
C0175906 (UMLS CUI [1,2])
C2348482 (UMLS CUI [2,1])
C0033131 (UMLS CUI [2,2])
C0175906 (UMLS CUI [1,2])
C2348482 (UMLS CUI [2,1])
C0033131 (UMLS CUI [2,2])
Informed Consent Refused
Item
refuses to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
C1705116 (UMLS CUI [1,2])
Study Subject Participation Status
Item
participating in a competing protocol or trial
boolean
C2348568 (UMLS CUI [1])