ID
36886
Descripción
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.
Link
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Versiones (4)
- 17/6/19 17/6/19 -
- 18/6/19 18/6/19 - Sarah Riepenhausen
- 30/4/20 30/4/20 - Sarah Riepenhausen
- 20/9/21 20/9/21 -
Titular de derechos de autor
ICHOM
Subido en
18 de junio de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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ICHOM Depression and Anxiety
Ongoing - Patient-Reported Form
- StudyEvent: ODM
Descripción
Prior Treatment
Alias
- UMLS CUI-1
- C1514463
Descripción
Inclusion Criteria: All patients If answered 'yes' to taking medication (TXMED) Timing: Ongoing Reporting Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0013216
Descripción
Treatment Variables
Alias
- UMLS CUI-1
- C0087111
Descripción
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 de datos
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0013227
Descripción
Inclusion criteria: All patients Timing: Ongoing Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0033968
Descripción
Inclusion criteria: All patients Timing: Ongoing Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0087111
- UMLS CUI [1,2]
- C0205394
Descripción
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 de datos
integer
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0013216
Descripción
Symptom Burden
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C2828008
Descripción
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo de datos
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
Descripción
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C2924103
Descripción
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0150079
Descripción
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0557875
- UMLS CUI [3]
- C0015672
Descripción
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0003621
Descripción
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0854366
Descripción
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0424099
Descripción
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0424114
- UMLS CUI [3]
- C0237280
Descripción
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0178360
Descripción
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2,1]
- C0001288
- UMLS CUI [2,2]
- C0033213
Descripción
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C0849963
- UMLS CUI [3]
- C0003467
Descripción
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2,1]
- C1298908
- UMLS CUI [2,2]
- C0243148
- UMLS CUI [2,3]
- C0233481
Descripción
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C0233481
Descripción
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3827766
Descripción
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3887611
Descripción
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3831378
Descripción
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3830159
Descripción
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2,1]
- C0001288
- UMLS CUI [2,2]
- C0033213
Descripción
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 de datos
integer
Alias
- UMLS CUI [1,1]
- C2919383
- UMLS CUI [1,2]
- C2964552
Descripción
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 de datos
integer
Alias
- UMLS CUI [1,1]
- C3472508
- UMLS CUI [1,2]
- C2964552
Descripción
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 de datos
integer
Alias
- UMLS CUI [1,1]
- C0034394
- UMLS CUI [1,2]
- C0038436
- UMLS CUI [1,3]
- C2964552
Descripción
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 de datos
integer
Alias
- UMLS CUI [1]
- C3472191
Descripción
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 de datos
integer
Alias
- UMLS CUI [1]
- C3472189
Descripción
Other
Alias
- UMLS CUI-1
- C0205394
Descripción
Inclusion Criteria: All patients Timing: Ongoing Reporting Source: Patient-reported Type: Single answer
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0392325
Descripción
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 de datos
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0043094
Descripción
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 de datos
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0549622
Descripción
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 de datos
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0037317
Descripción
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 de datos
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0043352
Descripción
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 de datos
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0013144
- UMLS CUI [3]
- C3179159
Descripción
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 de datos
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0007226
- UMLS CUI [3]
- C0030252
Descripción
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 de datos
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
Descripción
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 de datos
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0205394
Descripción
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 de datos
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0392325
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- StudyEvent: ODM
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