ID
36886
Descrizione
ICHOM Depression and Anxiety data collection Version 2.3.2 Revised: August 10th, 2018 International Consortium for Health Outcomes Measurement (ICHOM), Source: http://www.ichom.org/ For Depression and Anxiety, the following conditions and treatment approaches (or interventions) are covered by our Standard Set. This document contains the Ongoing - Patient-Reported Form. It has to be filled in between Baseline and Annually form. The ongoing periode includes e.g.: Active treatment stage; Measure essential PROs ongoing with treatment (potentially at every visit) Condition: Depression: Major Depressive Disorder | Dysthymia | Depressive Adaptive/Adjustment Disorder | Depressive Disorder - NOS Anxiety: Generalized Anxiety Disorder | Phobic Disorder | Agoraphobia | Post-Traumatic Stress Disorder | Panic Disorder | Obsessive-Compulsive Disorder Treatment Approaches : Psychopharmacotherapy | Psychotherapy | Lifestyle Interventions | Self-Guided Help | Other Forms of Therapy Collecting Clinician and Patient-Reported Outcome Measures: PHQ-9 (Patient Health Questionnaire). https://www.phqscreeners.com/ Pfizer: All PHQ, GAD-7 screeners and translations are downloadable from this website and no permission is required to reproduce, translate, display or distribute them. GAD-7 (Generalized Anxiety Disorder). https://www.phqscreeners.com/ Pfizer: All PHQ, GAD-7 screeners and translations are downloadable from this website and no permission is required to reproduce, translate, display or distribute them. Pfizer owner, authors: Drs. Spitzer, Williams and Kroenke SPIN (Social Phobia Inventory ), MIA (Mobility Inventory for Agoraphobia), IES-R (Impact of Event Scale - Revised for Post-traumatic Stress Disorder), PDSS-SR (Panic Disorder Severity Scale), OCI-R (Obsessive-Compulsive Inventory). As permission for use has to be obtained for all of these questionnaires from the copyright holder, only the total score will be included in this version of the standard set. WHODAS 2.0 (World Health Organization Disability Assessment Schedule 2.0). As there is a license needed for use of this questionnaire, only the total score will be included in this version oft he standard set. MOS-SSS (Medical Outcomes Study: Social Support Survey). There is no license or permission needed for use. https://www.rand.org/health-care/surveys_tools/mos/social-support.html ICHOM's Standard set was supported by the Douglas Institut universitaire en santé mentale and mental health university institute, Charité Universitätsmedizin Berlin, Stichting benchmark GGC.
collegamento
Keywords
versioni (4)
- 17/06/19 17/06/19 -
- 18/06/19 18/06/19 - Sarah Riepenhausen
- 30/04/20 30/04/20 - Sarah Riepenhausen
- 20/09/21 20/09/21 -
Titolare del copyright
ICHOM
Caricato su
18 giugno 2019
DOI
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Licenza
Creative Commons BY-NC 3.0
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ICHOM Depression and Anxiety
Ongoing - Patient-Reported Form
- StudyEvent: ODM
Descrizione
Prior Treatment
Alias
- UMLS CUI-1
- C1514463
Descrizione
Inclusion Criteria: All patients If answered 'yes' to taking medication (TXMED) Timing: Ongoing Reporting Source: Patient‐reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0013216
Descrizione
Treatment Variables
Alias
- UMLS CUI-1
- C0087111
Descrizione
Supporting Definition: Specific conditions include: Depression Generalized anxiety disorder Social phobia Agoraphobia Post-traumatic stress disorder Panic disorder Obsessive-compulsive disorder Inclusion criteria: All patients Timing: Ongoing Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0013227
Descrizione
Inclusion criteria: All patients Timing: Ongoing Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0033968
Descrizione
Inclusion criteria: All patients Timing: Ongoing Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0205394
Descrizione
Supporting definition: Specific conditions include: Depression Generalized anxiety disorder Social phobia Agoraphobia Post-traumatic stress disorder Panic disorder Obsessive-compulsive disorder Inclusion criteria: All patients If answered 'yes' to taking medication (DEPTXMEDON) Timing: Ongoing Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0013216
Descrizione
Symptom Burden
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C2828008
Descrizione
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2,1]
- C2984078
- UMLS CUI [2,2]
- C0543488
- UMLS CUI [3,1]
- C0679105
- UMLS CUI [3,2]
- C3668946
Descrizione
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C2924103
Descrizione
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0150079
Descrizione
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0557875
- UMLS CUI [3]
- C0015672
Descrizione
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0003621
Descrizione
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0854366
Descrizione
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0424099
Descrizione
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0424114
- UMLS CUI [3]
- C0237280
Descrizione
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0178360
Descrizione
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2,1]
- C0001288
- UMLS CUI [2,2]
- C0033213
Descrizione
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C0849963
- UMLS CUI [3]
- C0003467
Descrizione
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2,1]
- C1298908
- UMLS CUI [2,2]
- C0243148
- UMLS CUI [2,3]
- C0233481
Descrizione
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C0233481
Descrizione
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3827766
Descrizione
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3887611
Descrizione
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3831378
Descrizione
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3830159
Descrizione
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2,1]
- C0001288
- UMLS CUI [2,2]
- C0033213
Descrizione
As permission has to be obtained, the actual 17 questions of the SPIN questionnaire are not included in this version of the standard set. The ICHOM ID's are SPIN_Q01 to SPIN_Q17 Inclusion Criteria: Patients with social phobia Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C2919383
- UMLS CUI [1,2]
- C2964552
Descrizione
As permission has to be obtained, the actual 4 questions of the MI questionnaire are not included in this version of the standard set. The ICHOM ID's are MI_Q01, MI_Q01HIGH, MI_Q01OTHER, MI_Q02, MI_Q03a, MI_Q03b, MI_Q04a, MI_Q04b Supporting Definition: Each item corresponds to a separate VaraibleID. Inclusion Criteria: Patients with agoraphobia Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C3472508
- UMLS CUI [1,2]
- C2964552
Descrizione
As permission has to be obtained, the actual 22 questions of the IESR questionnaire are not included in this version of the standard set. The ICHOM ID's are IESR_Q01 to IESR_Q22 Inclusion Criteria: Patients with post-traumatic stress disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0034394
- UMLS CUI [1,2]
- C0038436
- UMLS CUI [1,3]
- C2964552
Descrizione
As permission has to be obtained, the actual 7 questions of the PDSSSR questionnaire are not included in this version of the standard set. The ICHOM ID's are PDSSSR_Q01 to PDSSSR_Q07 Inclusion Criteria: Patients with panic disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3472191
Descrizione
As permission has to be obtained, the actual 42 questions of the OCI questionnaire are not included in this version of the standard set. The ICHOM ID's are OCI_Q01 to OCI_Q42 Inclusion Criteria: Patients with obsessive-compulsive disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C3472189
Descrizione
Other
Alias
- UMLS CUI-1
- C0205394
Descrizione
Inclusion Criteria: All patients Timing: Ongoing Reporting Source: Patient-reported Type: Single answer
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0392325
Descrizione
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01ON) Timing: Ongoing Reporting Source: Patient-reported Type: Multiple answer Select all that apply In the case that more than one side‐effect is selected, split each response with a ‘;’
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0043094
Descrizione
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01ON) Timing: Ongoing Reporting Source: Patient-reported Type: Multiple answer Select all that apply In the case that more than one side‐effect is selected, split each response with a ‘;’
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0549622
Descrizione
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01ON) Timing: Ongoing Reporting Source: Patient-reported Type: Multiple answer Select all that apply In the case that more than one side‐effect is selected, split each response with a ‘;’
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0037317
Descrizione
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01ON) Timing: Ongoing Reporting Source: Patient-reported Type: Multiple answer Select all that apply In the case that more than one side‐effect is selected, split each response with a ‘;’
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0043352
Descrizione
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01ON) Timing: Ongoing Reporting Source: Patient-reported Type: Multiple answer Select all that apply In the case that more than one side‐effect is selected, split each response with a ‘;’
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0013144
- UMLS CUI [3]
- C3179159
Descrizione
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01ON) Timing: Ongoing Reporting Source: Patient-reported Type: Multiple answer Select all that apply In the case that more than one side‐effect is selected, split each response with a ‘;’
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0007226
- UMLS CUI [3]
- C0030252
Descrizione
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01ON) Timing: Ongoing Reporting Source: Patient-reported Type: Multiple answer Select all that apply In the case that more than one side‐effect is selected, split each response with a ‘;’
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0012240
- UMLS CUI [3]
- C0011991
- UMLS CUI [4]
- C0027497
- UMLS CUI [5]
- C0042963
Descrizione
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01ON) Timing: Ongoing Reporting Source: Patient-reported Type: Multiple answer Select all that apply In the case that more than one side‐effect is selected, split each response with a ‘;’
Tipo di dati
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0205394
Descrizione
Inclusion Criteria: All patients If answered 'Other' on type of medication side-effects (MEDSE_Q02ON888) Timing: Ongoing Reporting Source: Patient‐reported Type: Free text Response Options: Medication side-effect
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0392325
Similar models
Ongoing - Patient-Reported Form
- StudyEvent: ODM
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C0013227 (UMLS CUI [1,2])
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C0424099 (UMLS CUI [2])
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C0424114 (UMLS CUI [2])
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C0178360 (UMLS CUI [2])
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C0001288 (UMLS CUI [2,1])
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C0332218 (UMLS CUI-2)
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C0849963 (UMLS CUI [2])
C0003467 (UMLS CUI [3])
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C1298908 (UMLS CUI [2,1])
C0243148 (UMLS CUI [2,2])
C0233481 (UMLS CUI [2,3])
(Comment:en)
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C0233481 (UMLS CUI [2])
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C3887611 (UMLS CUI [2])
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C3831378 (UMLS CUI [2])
(Comment:en)
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C3830159 (UMLS CUI [2])
(Comment:en)
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C0001288 (UMLS CUI [2,1])
C0033213 (UMLS CUI [2,2])
C0332218 (UMLS CUI-2)
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C2964552 (UMLS CUI [1,2])
C2964552 (UMLS CUI [1,2])
C0038436 (UMLS CUI [1,2])
C2964552 (UMLS CUI [1,3])
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C0392325 (UMLS CUI [1,2])
C0043094 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C0549622 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C0037317 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C0043352 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])
C0013144 (UMLS CUI [2])
C3179159 (UMLS CUI [3])
C0392325 (UMLS CUI [1,2])
C0007226 (UMLS CUI [2])
C0030252 (UMLS CUI [3])
C0392325 (UMLS CUI [1,2])
C0012240 (UMLS CUI [2])
C0011991 (UMLS CUI [3])
C0027497 (UMLS CUI [4])
C0042963 (UMLS CUI [5])
C0392325 (UMLS CUI [1,2])
C0205394 (UMLS CUI [2])
C0392325 (UMLS CUI [1,2])