ID
40526
Descripción
LOCALIZED PROSTATE CANCER DATA COLLECTION Version 2.0.5 Revised: April 7th , 2017 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. Conditions: Localized prostate cancer Treatment Approaches: Active Surveillance | Watchful Waiting | Radical Prostatectomy* | External Beam Radiation Therapy* | Androgen Deprivation Therapy (ADT)* | Focal Therapy* | Other* * These should also be collected as salvage treatments where necessary This ODM-file contains Baseline Patient-reported Form. To be used at baseline, i.e., post-diagnosis, pre-treatment. Excluding the Patient Reported Outcome questionnaires (separate form, as asked at multiple timepoints). Please timestamp all variables. Some Standard Set variables are collected at multiple timepoints, and we will ask you to submit these variables in a concatenated VARIABLEID_TIMESTAMP form for future analyses. TEST StudyFor example, VARIABLEID_BASE (baseline); VARIABLEID_6MO (6 month follow-up); VARIABLEID_1YR (1 year follow-up), etc. Survey used: Expanded Prostate Cancer Index Composite (EPIC-26): The EPIC-26 is free for all health care organizations, and a license is not needed. The scoring guide may be found at http://www.med.umich.edu/urology/research/EPIC/EPIC-26-Scoring-1.2007.pdf ; Wei J, Dunn R, Litwin M, Sandler H, and Sanda M. "Development and Validation of the Expanded Prostate Cancer Index Composite (EPIC) for Comprehensive Assessment of Health-Related Quality of Life in Men with Prostate Cancer", Urology. 56: 899-905, 2000. For registries choosing to implement the EPIC-CP rather than the EPIC-26, we recommend using the same variable IDs as the corresponding EPIC-26 questions. This means that only questions 2, 3, 4a, 4b, 4d, 4e, 5, 6e, 6b, 7, 8b, 9, 12, 13a, 13c, and 13d of the EPIC-26 are administered. Utilization of Sexual Medications/Devices: The Utilization of Sexual Medications/Devices is free for all health care organizations, and a license is not needed. Refer to http://dx.doi.org/10.1016/j.urology.2006.01.077 for more information European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ- PR25): The EORTC QLQ-PR25 is free for all health care organizations, but a license is needed for use. Therefore it will not be integrated in this Version of the questionnaire. For more information, please visit http://groups.eortc.be/qol/eortc-qlq-c30 . ICHOM was supported for the Localized Prostate Cancer Standard Set by the Movember Foundation. Publication: Martin NE, Massey L, Stowell C, et al. Defining a standard set of patient-centered outcomes for men with localized prostate cancer. Eur Urol. 2015;67(3):460‐467. doi:10.1016/j.eururo.2014.08.075 For this version of the standard set, semantic annotation with UMLS CUIs has been added.
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Versiones (2)
- 21/8/18 21/8/18 - Sarah Riepenhausen
- 30/4/20 30/4/20 - Sarah Riepenhausen
Titular de derechos de autor
ICHOM
Subido en
30 de abril de 2020
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Licencia
Creative Commons BY-NC 4.0
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ICHOM Localized Prostate Cancer
Baseline Patient-reported Form
- StudyEvent: ODM
Descripción
Patient Factors
Alias
- UMLS CUI-1
- C1955348
Descripción
INCLUSION CRITERIA: All patients TIMING: Before treatment REPORTING SOURCE: Clinical or patient-reported TYPE: Date by DD/MM/YYYY RESPONSE OPTIONS: DD/MM/YYYY
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0001779
- UMLS CUI [2]
- C0421451
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C1298908
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0018799
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0020538
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C1306889
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0024115
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0011849
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0022658
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0023895
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0038454
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0027765
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C1707251
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0011581
Descripción
INCLUSION CRITERIA: All patients Based upon the Self-administered Comorbidity Questionnaire (Sangha et al, 2003) TIMING: Before treatment REPORTING SOURCE: patient-reported TYPE: Multiple Answer
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0003864
Similar models
Baseline Patient-reported Form
- StudyEvent: ODM
C0421451 (UMLS CUI [2])
C1298908 (UMLS CUI [1,2])
C0018799 (UMLS CUI [1,2])
C0020538 (UMLS CUI [1,2])
C1306889 (UMLS CUI [1,2])
C0024115 (UMLS CUI [1,2])
C0011849 (UMLS CUI [1,2])
C0022658 (UMLS CUI [1,2])
C0023895 (UMLS CUI [1,2])
C0038454 (UMLS CUI [1,2])
C0027765 (UMLS CUI [1,2])
C1707251 (UMLS CUI [1,2])
C0011581 (UMLS CUI [1,2])
C0003864 (UMLS CUI [1,2])