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Listed below are the details for the data element.

1.7
Element Type
Common Data Element
Informed consent obtained indicator
InfConsntObtInd
Short Description
Indicator of whether informed consent was obtained for the participant/subject to participate in the clinical research study
Definition
Indicator of whether informed consent was obtained for the participant/subject to participate in the clinical research study.
 

Biomedical Terminologies and Standards

Notes
cdRNS|FITBIR|PDBP;
Creation Date
Historical Notes
Informed consent obtained indicator
References
No references available

Data Type
Alphanumeric
Input Restrictions
Single Pre-Defined Value Selected
Pre-Defined Values
Population
Adult and Pediatric
Guidelines/Instructions
GENERAL: Choose one. If YES, record date informed consent was obtained.
Preferred Question Text
Was informed consent obtained?
Category Groups and Classifications
DiseaseDomainSub-Domain
General (For all diseases) Protocol Experience Participant/Subject Identification, Eligibility, and Enrollment

Classification

General (For all diseases) :
Core
Keywords
Labels
NINDS_CDE
Effective Date
Until Date
Last Change Date
Wed Jan 10 14:44:24 EST 2024
See Also
Submitting Organization Name
NIH/NINDS
Submitting Contact Name
NINDSCDE
Submitting Contact Information
NINDSCDE@emmes.com
Steward Organization Name
NIH/NINDS
Steward Contact Name
NINDSCDE
Steward Contact Information
NINDSCDE@emmes.com
NINDS ID

Change History