ID
44369
Beschrijving
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/ Notice: This work was conducted using resources from ICHOM, the International Consortium for Health Outcomes Measurement (www.ICHOM.org). The content is solely the responsibility of the authors and does not necessarily represent the official views of ICHOM. For Depression and Anxiety, the following conditions and treatment approaches (or interventions) are covered by our Standard Set. This document contains the Baseline - Patient-reported Form. It has to be filled in at Baseline(Treatment begin). 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. (and all other GAD or PHQ screeners); 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 This Standard set of ICHOM was supported by the Douglas mental health university institute, Charité Universitätsmedizin Berlin, Stichting benchmark GGC. Publication: Obbarius A, van Maasakkers L, Baer L, et al. Standardization of health outcomes assessment for depression and anxiety: recommendations from the ICHOM Depression and Anxiety Working Group. Qual Life Res. 2017;26(12):3211–3225. doi:10.1007/s11136-017-1659-5 For this version of the standard set, semantic annotation with UMLS CUIs has been added.
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Trefwoorden
Versies (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 -
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ICHOM
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ICHOM Depression and Anxiety
Baseline - Patient-reported Form
- StudyEvent: ODM
Beschrijving
Demographic factors
Alias
- UMLS CUI-1
- C1704791
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Date by DD/MM/YYYY Response Options: DD/MM/YYYY
Datatype
date
Maateenheden
- DD/MM/YYYY
Alias
- UMLS CUI [1]
- C0001779
- UMLS CUI [2]
- C0421451
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0079399
Beschrijving
Supporting Definition: The level of schooling is defined in each country as per ISCED [International Standard Classification] Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0013658
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C2184149
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0014003
- UMLS CUI [1,2]
- C0449438
Beschrijving
As Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3829137
- UMLS CUI [2]
- C3827363
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3829137
- UMLS CUI [2]
- C3827984
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3829137
- UMLS CUI [2]
- C4034911
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3829137
- UMLS CUI [2,1]
- C0027361
- UMLS CUI [2,2]
- C0024028
Beschrijving
Health status
Alias
- UMLS CUI-1
- C0018759
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1547647
- UMLS CUI [1,2]
- C0679138
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2,1]
- C1298908
- UMLS CUI [2,2]
- C2359476
Beschrijving
Supporting Definition: Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0018799
- UMLS CUI [3]
- C0018801
- UMLS CUI [4]
- C0002962
- UMLS CUI [5]
- C0027051
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0020538
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C1306889
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0024115
- UMLS CUI [3]
- C0004096
- UMLS CUI [4]
- C0008677
- UMLS CUI [5]
- C0034067
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0011849
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0022658
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0023895
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2,1]
- C0038454
- UMLS CUI [2,2]
- C0678227
- UMLS CUI [2,3]
- C1546466
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0027765
- UMLS CUI [3]
- C0030567
- UMLS CUI [4]
- C0026769
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0006826
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0011581
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0003864
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0038586
- UMLS CUI [3]
- C0013146
- UMLS CUI [4]
- C0001975
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2,1]
- C0037650
- UMLS CUI [2,2]
- C3839861
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0031212
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C1298685
Beschrijving
Supporting Definition: Based upon the Self‐administered Comorbidity Questionnaire (Sangha et al, 2003) Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Multiple answer Separate multiple entries with ";"
Datatype
boolean
Alias
- UMLS CUI [1]
- C0009488
- UMLS CUI [2]
- C0036341
Beschrijving
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: Baseline Reporting Source: Patient-reported Type: Numerical value Response Options: Numerical value of number of months
Datatype
integer
Alias
- UMLS CUI [1]
- C0436359
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0332189
- UMLS CUI [1,2]
- C0011581
- UMLS CUI [1,3]
- C0332152
Beschrijving
Prior Treatment
Alias
- UMLS CUI-1
- C1514463
Beschrijving
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: Baseline, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1514463
- UMLS CUI [1,2]
- C0013227
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1514463
- UMLS CUI [1,2]
- C0033968
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1514463
- UMLS CUI [1,2]
- C0205394
Beschrijving
Inclusion Criteria: All patients If answered 'yes' to taking medication (TXMED) Timing: Baseline Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1321605
- UMLS CUI [1,2]
- C0013216
Beschrijving
Symptom Burden
Alias
- UMLS CUI-1
- C1457887
- UMLS CUI-2
- C2828008
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
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
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C2924103
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0150079
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0849970
- UMLS CUI [3]
- C0015672
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0003621
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0854366
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0424099
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0424114
- UMLS CUI [3]
- C0237280
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2]
- C0178360
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Ongoing, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C4083201
- UMLS CUI [2,1]
- C0001288
- UMLS CUI [2,2]
- C0033213
Beschrijving
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C0849963
- UMLS CUI [3]
- C0003467
Beschrijving
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2,1]
- C1298908
- UMLS CUI [2,2]
- C0243148
- UMLS CUI [2,3]
- C0233481
Beschrijving
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C0233481
Beschrijving
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3827766
Beschrijving
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3887611
Beschrijving
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3831378
Beschrijving
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2]
- C3830159
Beschrijving
Inclusion Criteria: Patients with generalized anxiety disorder Timing: Baseline, Ongoing, Annually Reporting Source: Patient‐reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C3641330
- UMLS CUI [2,1]
- C0001288
- UMLS CUI [2,2]
- C0033213
Beschrijving
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
Datatype
integer
Alias
- UMLS CUI [1,1]
- C2919383
- UMLS CUI [1,2]
- C2964552
Beschrijving
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
Datatype
integer
Alias
- UMLS CUI [1,1]
- C3472508
- UMLS CUI [1,2]
- C2964552
Beschrijving
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
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0034394
- UMLS CUI [1,2]
- C0038436
- UMLS CUI [1,3]
- C2964552
Beschrijving
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
Datatype
integer
Alias
- UMLS CUI [1]
- C3472191
Beschrijving
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
Datatype
integer
Alias
- UMLS CUI [1]
- C3472189
Beschrijving
Functioning
Beschrijving
As license is needed for use of this questionnaire, the actual 12 questions of the WHODAS 2.0 questionnaire are not included in this version of the standard set. The ICHOM ID's are WHODAS_Q01 to WHODAS_Q12 Inclusion criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1,1]
- C4321496
- UMLS CUI [1,2]
- C2964552
Beschrijving
Recovery Speed and Health Sustainability
Alias
- UMLS CUI-1
- C2004454
- UMLS CUI-2
- C0018759
Beschrijving
Inclusion Criteria: All patients Timing: Baseline, Annually Reporting Source: Patient-reported Type: Numerical value Response Options: Numerical value of number of days
Datatype
integer
Maateenheden
- days
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0000849
Beschrijving
Other
Alias
- UMLS CUI-1
- C0205394
Beschrijving
Inclusion Criteria: All patients Timing: Baseline Reporting Source: Patient-reported Type: Single answer
Datatype
integer
Alias
- UMLS CUI [1]
- C0392325
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01) Timing: Baseline 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 ‘;’
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0043094
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01) Timing: Baseline 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 ‘;’
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0549622
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01) Timing: Baseline 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 ‘;’
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0037317
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01) Timing: Baseline 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 ‘;’
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0043352
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01) Timing: Baseline 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 ‘;’
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0013144
- UMLS CUI [3]
- C3179159
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01) Timing: Baseline 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 ‘;’
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0007226
- UMLS CUI [3]
- C0030252
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01) Timing: Baseline 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 ‘;’
Datatype
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
Beschrijving
Inclusion Criteria: All patients If answered 'yes' on medication side-effects (MEDSE_Q01) Timing: Baseline 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 ‘;’
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0332307
- UMLS CUI [1,2]
- C0392325
- UMLS CUI [2]
- C0205394
Beschrijving
Inclusion Criteria: All patients If answered 'Other' on type of medication side-effects (MEDSE_Q02_888) Timing: Baseline Reporting Source: Patient‐reported Type: Free text Response Options: Medication side-effect
Datatype
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0392325
Similar models
Baseline - Patient-reported Form
- StudyEvent: ODM
C0421451 (UMLS CUI [2])
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C0508431 (UMLS CUI-2)
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C0033145 (UMLS CUI-2)
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C2184147 (UMLS CUI-2)
C0557130 (UMLS CUI-3)
C0557128 (UMLS CUI-4)
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C0557218 (UMLS CUI-2)
C3640869 (UMLS CUI-3)
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C0449438 (UMLS CUI [1,2])
C0332300 (UMLS CUI-2)
C0003467 (UMLS CUI-3)
C0011581 (UMLS CUI-4)
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C0003467 (UMLS CUI-2)
C0011581 (UMLS CUI-3)
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C0041674 (UMLS CUI-2)
C0038492 (UMLS CUI-3)
C0035345 (UMLS CUI-4)
C0555052 (UMLS CUI-5)
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C2984044 (UMLS CUI-2)
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C3827363 (UMLS CUI [2])
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C3827984 (UMLS CUI [2])
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C4034911 (UMLS CUI [2])
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C0027361 (UMLS CUI [2,1])
C0024028 (UMLS CUI [2,2])
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C0679138 (UMLS CUI [1,2])
C1272703 (UMLS CUI-2)
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C1272703 (UMLS CUI-2)
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C1272703 (UMLS CUI-2)
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C1272703 (UMLS CUI-2)
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C1298908 (UMLS CUI [2,1])
C2359476 (UMLS CUI [2,2])
C0018799 (UMLS CUI [2])
C0018801 (UMLS CUI [3])
C0002962 (UMLS CUI [4])
C0027051 (UMLS CUI [5])
C0020538 (UMLS CUI [2])
C1306889 (UMLS CUI [2])
C0024115 (UMLS CUI [2])
C0004096 (UMLS CUI [3])
C0008677 (UMLS CUI [4])
C0034067 (UMLS CUI [5])
C0011849 (UMLS CUI [2])
C0022658 (UMLS CUI [2])
C0023895 (UMLS CUI [2])
C0038454 (UMLS CUI [2,1])
C0678227 (UMLS CUI [2,2])
C1546466 (UMLS CUI [2,3])
C0027765 (UMLS CUI [2])
C0030567 (UMLS CUI [3])
C0026769 (UMLS CUI [4])
C0006826 (UMLS CUI [2])
C0011581 (UMLS CUI [2])
C0003864 (UMLS CUI [2])
C0038586 (UMLS CUI [2])
C0013146 (UMLS CUI [3])
C0001975 (UMLS CUI [4])
C0037650 (UMLS CUI [2,1])
C3839861 (UMLS CUI [2,2])
C0031212 (UMLS CUI [2])
C1298685 (UMLS CUI [2])
C0036341 (UMLS CUI [2])
C0011581 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
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C0205163 (UMLS CUI-2)
C0332189 (UMLS CUI-3)
C0011581 (UMLS CUI-4)
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C0205163 (UMLS CUI-2)
C0332189 (UMLS CUI-3)
C0011581 (UMLS CUI-4)
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C2745955 (UMLS CUI-2)
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C0013227 (UMLS CUI [1,2])
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C0205447 (UMLS CUI-2)
C0439231 (UMLS CUI-3)
C0439092 (UMLS CUI-4)
C0205449 (UMLS CUI-5)
C0439231 (UMLS CUI-6)
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C0205449 (UMLS CUI-2)
C0439231 (UMLS CUI-3)
C0439092 (UMLS CUI-4)
C0205452 (UMLS CUI-5)
C0439231 (UMLS CUI-6)
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C0205452 (UMLS CUI-2)
C0439231 (UMLS CUI-3)
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C0033968 (UMLS CUI [1,2])
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C0205447 (UMLS CUI-2)
C0439231 (UMLS CUI-3)
C0439092 (UMLS CUI-4)
C0205449 (UMLS CUI-5)
C0439231 (UMLS CUI-6)
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C0205449 (UMLS CUI-2)
C0439231 (UMLS CUI-3)
C0439092 (UMLS CUI-4)
C0205452 (UMLS CUI-5)
C0439231 (UMLS CUI-6)
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C0205452 (UMLS CUI-2)
C0439231 (UMLS CUI-3)
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C0205447 (UMLS CUI-2)
C0439231 (UMLS CUI-3)
C0439092 (UMLS CUI-4)
C0205449 (UMLS CUI-5)
C0439231 (UMLS CUI-6)
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C0205449 (UMLS CUI-2)
C0439231 (UMLS CUI-3)
C0439092 (UMLS CUI-4)
C0205452 (UMLS CUI-5)
C0439231 (UMLS CUI-6)
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C0205452 (UMLS CUI-2)
C0439231 (UMLS CUI-3)
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C0013216 (UMLS CUI [1,2])
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C2984078 (UMLS CUI [2,1])
C0543488 (UMLS CUI [2,2])
C0679105 (UMLS CUI [3,1])
C3668946 (UMLS CUI [3,2])
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C2924103 (UMLS CUI [2])
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C0150079 (UMLS CUI [2])
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C0849970 (UMLS CUI [2])
C0015672 (UMLS CUI [3])
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C0003621 (UMLS CUI [2])
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C0854366 (UMLS CUI [2])
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C0424099 (UMLS CUI [2])
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C0424114 (UMLS CUI [2])
C0237280 (UMLS CUI [3])
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C0178360 (UMLS CUI [2])
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C0001288 (UMLS CUI [2,1])
C0033213 (UMLS CUI [2,2])
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])
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C0233481 (UMLS CUI [2])
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C3887611 (UMLS CUI [2])
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C3831378 (UMLS CUI [2])
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C3830159 (UMLS CUI [2])
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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])
C2964552 (UMLS CUI [1,2])
C0018759 (UMLS CUI-2)
C0000849 (UMLS CUI [1,2])
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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])