Major Depressive Disorder Primary
Item
primary dsm-iv diagnosis of major depressive disorder by clinical interview
boolean
C1269683 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
Hamilton rating scale for depression
Item
score of greater than 12 on ham-d
boolean
C0451203 (UMLS CUI [1])
Delivery
Item
delivery of an infant within the 12 months prior to study entry
boolean
C0005615 (UMLS CUI [1])
Able to speak English Language | Able to read English Language | Clinical Trial procedure Completion
Item
able to speak and read english sufficiently to complete the study procedures
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0586740 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0008976 (UMLS CUI [3,1])
C0184661 (UMLS CUI [3,2])
C0205197 (UMLS CUI [3,3])
Contraceptive methods Willing
Item
willing to use effective birth control methods throughout the study
boolean
C0700589 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
Gender | Infant Death
Item
woman whose infant has died prior to study entry
boolean
C0079399 (UMLS CUI [1])
C0549159 (UMLS CUI [2])
Bipolar Disorder | Schizophrenia | Psychotic Disorders
Item
current or past diagnosis of bipolar disorder, schizophrenia or other psychotic disorder;
boolean
C0005586 (UMLS CUI [1])
C0036341 (UMLS CUI [2])
C0033975 (UMLS CUI [3])
Substance Use Disorders | Substance Dependence | Exception Nicotine | Anorexia
Item
diagnosis of alcohol or drug abuse or dependence (except nicotine) or anorexia in the past year;
boolean
C0038586 (UMLS CUI [1])
C0038580 (UMLS CUI [2])
C1705847 (UMLS CUI [3,1])
C0028040 (UMLS CUI [3,2])
C0003123 (UMLS CUI [4])
Psychotic symptom
Item
psychotic symptoms;
boolean
C0871189 (UMLS CUI [1])
At risk for suicide | At risk Homicide
Item
acute suicidal or homicidal risks;
boolean
C0563664 (UMLS CUI [1])
C1444641 (UMLS CUI [2,1])
C0019872 (UMLS CUI [2,2])
Gender | Antidepressive Agents
Item
women who have been on an antidepressant for more than 14 days prior to consent, (if less than 14 days and willing to taper off, will be eligible to continue once tapered off);
boolean
C0079399 (UMLS CUI [1])
C0003289 (UMLS CUI [2])
Gender | Anti-Anxiety Agents | Benzodiazepines | Buspirone | Plant Preparations Psychoactive | Hypericum perforatum | Fish Oil
Item
women on daily anxiolytic medication (i.e. benzodiazepine, buspirone) or daily psychoactive herbal preparation (st. john's wort or fish oil) (if willing to discontinue these substances may be eligible once they have been tapered off);
boolean
C0079399 (UMLS CUI [1])
C0040616 (UMLS CUI [2])
C0005064 (UMLS CUI [3])
C0006462 (UMLS CUI [4])
C0949854 (UMLS CUI [5,1])
C0682880 (UMLS CUI [5,2])
C0936242 (UMLS CUI [6])
C0016157 (UMLS CUI [7])
Pharmaceutical Preparations Dosage Frequency | Lunesta | Eszopiclone | Ambien | Zolpidem | Ambien CR | Lorazepam | Benzodiazepine Dosage Equivalent | Sonata | Zaleplon | Rozerem | Ramelteon
Item
medications taken prn over the listed dose and frequency (women will still be eligible if they take: lunesta/eszopiclone 3 mg or less, up to 3 nights a week, ambien/zolpidem 5mg or less, ambien cr 6.25 mg or less, up to 3 nights a week, lorazepam or equivalent benzodiazepine dose: 0.5 mg up to 3 nights a week, sonata/zaleplon: 5 mg or less, up to 3 nights a week, rozerem/ramelteon: 8 mg or less, up to 3 nights a week);
boolean
C0013227 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C3476109 (UMLS CUI [1,3])
C1579761 (UMLS CUI [2])
C1436328 (UMLS CUI [3])
C0487782 (UMLS CUI [4])
C0078839 (UMLS CUI [5])
C1644791 (UMLS CUI [6])
C0024002 (UMLS CUI [7])
C4048284 (UMLS CUI [8,1])
C0178602 (UMLS CUI [8,2])
C0205163 (UMLS CUI [8,3])
C0876170 (UMLS CUI [9])
C0251504 (UMLS CUI [10])
C1621477 (UMLS CUI [11])
C1565316 (UMLS CUI [12])
Antidepressive Agents Sleeplessness | Desyrel | Trazodone | Elavil | Amitriptyline | Remeron | Mirtazapine
Item
if they take antidepressants prn for insomnia (eg: desyrel/trazodone, elavil/amitriptyline, remeron/mirtazapine;
boolean
C0003289 (UMLS CUI [1,1])
C0917801 (UMLS CUI [1,2])
C0701914 (UMLS CUI [2])
C0040805 (UMLS CUI [3])
C0087119 (UMLS CUI [4])
C0002600 (UMLS CUI [5])
C0525726 (UMLS CUI [6])
C0049506 (UMLS CUI [7])
Psychotherapy
Item
ongoing concurrent psychotherapeutic treatment or psychotherapeutic treatment within the last month;
boolean
C0033968 (UMLS CUI [1])
Psychiatric symptom Requirement Psychiatric therapeutic procedure Specialized
Item
psychiatric symptoms requiring specialized psychiatric treatment;
boolean
C0233401 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0204523 (UMLS CUI [1,3])
C1704211 (UMLS CUI [1,4])
Disease | Medical contraindication Sertraline
Item
significant medical disorder that would make sertraline treatment contra-indicated,
boolean
C0012634 (UMLS CUI [1])
C1301624 (UMLS CUI [2,1])
C0074393 (UMLS CUI [2,2])
Study Subject Participation Status | Interpersonal psychotherapy | Sertraline Dosage Frequency
Item
previous trial of ipt therapy with a certified ipt therapist or an adequate trial of sertraline (i.e. at least 8 weeks of at least 100 mg daily of sertraline).
boolean
C2348568 (UMLS CUI [1])
C0871787 (UMLS CUI [2])
C0074393 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
C0439603 (UMLS CUI [3,3])