0 Bedömningar

ID

13688

Beskrivning

Halifax Treatment Refractory Depression Trial; ODM derived from: https://clinicaltrials.gov/show/NCT01141426

Länk

https://clinicaltrials.gov/show/NCT01141426

Nyckelord

  1. 2016-02-28 2016-02-28 -
Uppladdad den

28 februari 2016

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :


    Inga kommentarer

    Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

    Eligibility Depression NCT01141426

    Eligibility Depression NCT01141426

    1. StudyEvent: Eligibility
      1. Eligibility Depression NCT01141426
    Inclusion Criteria
    Beskrivning

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    patients aged 18 - 65 years.
    Beskrivning

    age

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    patients must identify depression as their primary problem (rather than being secondary to other mental health diagnosis).
    Beskrivning

    primary disorders depression

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0277554
    UMLS CUI [1,2]
    C0011581
    any dsm-iv diagnosis of major depression as assessed by the mini neuropsychiatric interview plus (m.i.n.i. plus) at time of research intake interview.
    Beskrivning

    dsm-iv; major depression

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0220952
    UMLS CUI [2]
    C1269683
    patients will have had at least one treatment trial of antidepressants at an acceptable therapeutic dose (length ≥ 6 weeks) for the current depressive episode without adequate response (score on the hamilton rating scale for depression ≥ 16 ) at time of screening interview.
    Beskrivning

    antidepressant; Hamilton rating scale for depression

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0003289
    UMLS CUI [2]
    C0451203
    patients will not have started new medications in the previous ≥ 6 weeks, or have received psychotherapy treatment in the 12 months prior to being invited to participate in the study.
    Beskrivning

    psychotherapy

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0033968
    participants will agree to video-taped sessions and will consent to the investigator accessing their information in clinical files and hospital database (e.g., medications, number of visits to health care professionals).
    Beskrivning

    informed consent

    Datatyp

    boolean

    Alias
    UMLS CUI [1]
    C0021430
    Exclusion Criteria
    Beskrivning

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    psychotic depression, bipolar depression, substance dependence, severe cluster a or b personality disorders, active suicidality, or cognitive impairment: such that patients require an intervention other than psychotherapy (as per the current protocol for the experimental treatment arm) or patients unable to give consent to treatment.
    Beskrivning

    Compliance behavior Limited Comorbidity

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C1321605
    UMLS CUI [1,2]
    C0439801
    UMLS CUI [1,3]
    C0009488
    patients with depression due to a general medical condition or secondary to a comorbid mental health or psychosocial condition will be excluded.
    Beskrivning

    Secondary disease depression

    Datatyp

    boolean

    Alias
    UMLS CUI [1,1]
    C0277555
    UMLS CUI [1,2]
    C0011581

    Similar models

    Eligibility Depression NCT01141426

    1. StudyEvent: Eligibility
      1. Eligibility Depression NCT01141426
    Name
    Typ
    Description | Question | Decode (Coded Value)
    Datatyp
    Alias
    Item Group
    C1512693 (UMLS CUI)
    age
    Item
    patients aged 18 - 65 years.
    boolean
    C0001779 (UMLS CUI [1])
    primary disorders depression
    Item
    patients must identify depression as their primary problem (rather than being secondary to other mental health diagnosis).
    boolean
    C0277554 (UMLS CUI [1,1])
    C0011581 (UMLS CUI [1,2])
    dsm-iv; major depression
    Item
    any dsm-iv diagnosis of major depression as assessed by the mini neuropsychiatric interview plus (m.i.n.i. plus) at time of research intake interview.
    boolean
    C0220952 (UMLS CUI [1])
    C1269683 (UMLS CUI [2])
    antidepressant; Hamilton rating scale for depression
    Item
    patients will have had at least one treatment trial of antidepressants at an acceptable therapeutic dose (length ≥ 6 weeks) for the current depressive episode without adequate response (score on the hamilton rating scale for depression ≥ 16 ) at time of screening interview.
    boolean
    C0003289 (UMLS CUI [1])
    C0451203 (UMLS CUI [2])
    psychotherapy
    Item
    patients will not have started new medications in the previous ≥ 6 weeks, or have received psychotherapy treatment in the 12 months prior to being invited to participate in the study.
    boolean
    C0033968 (UMLS CUI [1])
    informed consent
    Item
    participants will agree to video-taped sessions and will consent to the investigator accessing their information in clinical files and hospital database (e.g., medications, number of visits to health care professionals).
    boolean
    C0021430 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Compliance behavior Limited Comorbidity
    Item
    psychotic depression, bipolar depression, substance dependence, severe cluster a or b personality disorders, active suicidality, or cognitive impairment: such that patients require an intervention other than psychotherapy (as per the current protocol for the experimental treatment arm) or patients unable to give consent to treatment.
    boolean
    C1321605 (UMLS CUI [1,1])
    C0439801 (UMLS CUI [1,2])
    C0009488 (UMLS CUI [1,3])
    Secondary disease depression
    Item
    patients with depression due to a general medical condition or secondary to a comorbid mental health or psychosocial condition will be excluded.
    boolean
    C0277555 (UMLS CUI [1,1])
    C0011581 (UMLS CUI [1,2])

    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