ID

19203

Description

PCORnet Common Data Model (CDM) PCORNET Trial PCORnet Common Data Model (CDM) A patient-centered approach to building an agile research platform is at the heart of PCORnet, and data serves as the backbone. Considering the large number and diverse types of organizations that are part of PCORnet, we all benefit from having a streamlined, efficient way to use the data produced by these organizations. Enter the PCORnet Common Data Model. The Common Data Model (or CDM) is a way of organizing data into a standard structure. The approach PCORnet is using to do this mirrors the approaches used by other large national research consortia. Each PCORnet partner network maps data to the same consistent format (i.e., with the same variable name, attributes, and other metadata). By undertaking this step, we create a platform that enables much more rapid responses to research-related questions. Contrast this with having to transform and prepare data each time we want to ask a new research question, and the efficiencies become clear. The PCORnet CDM is based on the FDA Sentinel Initiative Common Data Model (www.sentinelsystem.org) and has been informed by other distributed initiatives such as the Health Care Systems Research Network, the Vaccine Safety Datalink, various AHRQ Distributed Research Network projects, and the ONC Standards & Interoperability Framework Query Health Initiative. The PCORnet CDM leverages standard terminologies and coding systems for healthcare (including ICD, SNOMED, CPT, HCPSC, and LOINC) to enable interoperability with and responsiveness to evolving data standards. The PCORnet CDM (like other parts of PCORnet) will grow and evolve. Version 1.0 focused on a set of data items that are frequently available. Subsequent versions build in additional data elements which are analytically important for patient-centered outcomes research and feasible to standardize across sites.

Lien

www.sentinelsystem.org

Mots-clés

  1. 12/12/2016 12/12/2016 -
  2. 01/07/2019 01/07/2019 -
  3. 30/03/2020 30/03/2020 -
Téléchargé le

12 décembre 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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PCORnet Common Data Model (CDM) PCORNET Trial

PCORnet Common Data Model (CDM) PCORNET Trial

PCORNET Trial
Description

PCORNET Trial

Alias
UMLS CUI-1
C0008976
Patient ID
Description

Arbitrary person-level identifier used to link across tables.

Type de données

integer

Alias
UMLS CUI [1]
C2348585
Trial ID
Description

Each TRIALID is assigned by the PCORnet trial’s coordinating center.

Type de données

integer

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C1300638
Participant ID
Description

Arbitrary person-level identifier used to uniquely identify a participant in a PCORnet trial. PARTICIPANTID is never repeated or reused for a specific clinical trial, and is generally assigned by trial-specific processes. It may be the same as a randomization ID.

Type de données

text

Alias
UMLS CUI [1,1]
C0679646
UMLS CUI [1,2]
C1300638
UMLS CUI [2]
C2348585
Trial Site ID
Description

Each TRIAL_SITEID is assigned by the PCORnet trial coordinating center.

Type de données

text

Alias
UMLS CUI [1,1]
C0450429
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C1300638
Trial Enroll Date
Description

Date on which the participant enrolled in the trial (generally coincides with trial consent process).

Type de données

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0679646
UMLS CUI [1,3]
C1516879
Trial End Date
Description

Date on which the participant completes participation in the trial.

Type de données

date

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C1272693
UMLS CUI [1,3]
C0011008
UMLS CUI [2,1]
C0008976
UMLS CUI [2,2]
C0806020
Trial Withdraw Date
Description

If applicable, date on which the participant withdraws consent from the trial.

Type de données

date

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C2349954
UMLS CUI [1,3]
C0011008
Trial Invite Code
Description

Textual strings used to uniquely identify invitations sent to potential participants, and allows acceptances to be associated back to the originating source. Where used, there should generally be a unique combination of PATID, TRIAL_NAME, and INVITE_CODE within each datamart. For example, this might include “co-enrollment ID strings” for e-mail invites or “verification codes” for letter invites.

Type de données

text

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C2826348
UMLS CUI [1,3]
C0805701

Similar models

PCORnet Common Data Model (CDM) PCORNET Trial

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
PCORNET Trial
C0008976 (UMLS CUI-1)
Patient ID
Item
Patient ID
integer
C2348585 (UMLS CUI [1])
Trial ID
Item
Trial ID
integer
C0008976 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
Participant ID
Item
Participant ID
text
C0679646 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
C2348585 (UMLS CUI [2])
Trial Site ID
Item
Trial Site ID
text
C0450429 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C1300638 (UMLS CUI [1,3])
Trial Enroll Date
Item
Trial Enroll Date
date
C0011008 (UMLS CUI [1,1])
C0679646 (UMLS CUI [1,2])
C1516879 (UMLS CUI [1,3])
Trial End Date
Item
Trial End Date
date
C0008976 (UMLS CUI [1,1])
C1272693 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0008976 (UMLS CUI [2,1])
C0806020 (UMLS CUI [2,2])
Trial Withdraw Date
Item
Trial Withdraw Date
date
C0008976 (UMLS CUI [1,1])
C2349954 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Trial Invite Code
Item
Trial Invite Code
text
C0008976 (UMLS CUI [1,1])
C2826348 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,3])

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