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ID
20794
Beschrijving
Depression in Older Adults; ODM derived from: https://clinicaltrials.gov/show/NCT00643162
Link
https://clinicaltrials.gov/show/NCT00643162
Trefwoorden
Versies (1)
- 18-03-17 18-03-17 -
Geüploaded op
18 maart 2017
DOI
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Creative Commons BY 4.0
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Eligibility Depression NCT00643162
Eligibility Depression NCT00643162
- StudyEvent: Eligibility
Similar models
Eligibility Depression NCT00643162
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
1. > 60 years of age
boolean
C0001779 (UMLS CUI [1])
Unipolar major depression
Item
2. unipolar major depression as defined by structured clinical interaction dsm-iv (scid)
boolean
C1269683 (UMLS CUI [1])
Hamilton Rating Scale
Item
3. ham-d score of > 17 (21-item scale)]]
boolean
C0451203 (UMLS CUI [1])
Antidepressive Therapy
Item
4. not taking antidepressants for at least two weeks, 2 months for fluoxetine and maois]]
boolean
C0003289 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
Informed Consent
Item
5. capable of giving informed consent.
boolean
C0021430 (UMLS CUI [1])
Unable to give informed consent
Item
1. unable to provide informed consent (e.g. severe cognitive impairment)
boolean
C1299582 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
Medical condition requiring medical treatment
Item
2. acute medical condition or exacerbation of chronic medical condition associated with significant distress (pain, protracted fevers, etc.) and requiring active medical treatment.
boolean
C0012634 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,2])
High risk of suicide
Item
3. high risk of suicide or violence as assessed by the investigator
boolean
C1271074 (UMLS CUI [1])
Psychosis or bipolar disorder
Item
4. current or past history of psychosis or bipolar disorder
boolean
C0033975 (UMLS CUI [1])
C0005586 (UMLS CUI [2])
C0005586 (UMLS CUI [2])
Psychotropic medication and/or psychotherapy
Item
5. use of psychotropic medication and/or psychotherapy outside of the study
boolean
C0033978 (UMLS CUI [1])
C0033968 (UMLS CUI [2])
C0033968 (UMLS CUI [2])
Pharmacotherapy
Item
6. (exposure to treatment of fluoxetine or maois in the previous two months; chronic use of benzodiazepine and non-benzodiazepine sedatives, antipsychotics, psychostimulants, mood stabilizing agents, codeine, steroids, anti-inflammatory agents.
boolean
C0013216 (UMLS CUI [1])
Alternative medicine
Item
7. alternative medicine use in the preceding 30 days (e.g. acupuncture, herbs, etc.)
boolean
C0002346 (UMLS CUI [1])
Contraindication to massage
Item
8. history of intolerance to massage or contraindication to massage (e.g. skin lesions that prevent direct contact by the therapist)
boolean
C0024875 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C1301624 (UMLS CUI [1,2])
Mental disorder
Item
9. diagnosis of schizophrenia, schizophreniform disorder, schizoaffective disorder, schizotypal disorder, psychotic depression or bipolar disorders;
boolean
C0004936 (UMLS CUI [1])
MMSE
Item
10. mmse less than 22
boolean
C0451306 (UMLS CUI [1])
Alzheimer's disease assessment
Item
11. alzheimer's disease assessment scale-cognitive subscale ³ greater than 12
boolean
C0002395 (UMLS CUI [1])
Substance Use Disorder
Item
12. current drug or alcohol abuse or dependence or history of drug or alcohol abuse or dependence within the past 6 months
boolean
C0038586 (UMLS CUI [1])
Unstable status
Item
13. unstable medical or neurological conditions that are likely to interfere with the treatment of depression
boolean
C0443343 (UMLS CUI [1])
Psychotropic pharmacotherapy
Item
14. currently on psychotropic medications including antidepressants or neuroleptics
boolean
C0033978 (UMLS CUI [1])
Safety issue
Item
15. active suicidal ideation or other safety issues determined by the clinician to not be suitable for inclusion in the study
boolean
C2911688 (UMLS CUI [1])