CDE Catalog | NINDS Common Data Elements

***Please contact the NINDS CDE Team (NINDSCDE@emmes.com) if you encounter any search difficulties.***

The CDE Catalog is a directory of the available NINDS CDEs. Users can search the Catalog to isolate a subset of the CDEs (e.g., all stroke-specific CDEs, etc.), and to view and download details about the CDEs.

Select any filter below to search the CDE Catalog.

For best results, clear form between searches. In addition, when specifying NeuroRehab, Sport-Related Concussion (SRC) or Traumatic Brain Injury (TBI) as the Disease, please select a Subdisease as well.

NeuroRehab Comprehensive includes all NeuroRehab CDE recommendations. NeuroRehab General includes all NeuroRehab CDE recommendations that are not disease specific. All other NeuroRehab Subdiseases include recommendations specific to existing NINDS CDE project disorders.

Choose your Time Frame for your SRC study (Acute (time of injury until 72 hours), Subacute (after 72 hours to 3 months), and Persistent/Chronic (3 months and greater post-concussion) or Comprehensive if your study falls across the study time frames.

Choose your type of TBI study (Acute Hospitalized, Concussion/Mild TBI, Moderate/Severe TBI: Rehabilitation, or Epidemiology) or Comprehensive if your study falls outside of the study types or incorporates aspects of more than one type of study.

Search Form

CRF Name

Displaying 101 - 125 of 883

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Operations

Selected 25 rows in this page.

The search results below can be downloaded by clicking the checkboxes on the far left side of the table. Select the header checkbox to select all CDEs listed on the first page. Then choose CDE Detailed Report from the Choose an operation dropdown menu.
Select all	CDE ID	CDE Name	Definition	Classification	CRF Name	Copyrighted or trademarked	Disease Name	Subdisease Name
F1807-C00322	C00322	Medical history condition text	Verbatim text for the medical condition/disease reported by the participant/subject or documented in the medical record as part of medical history	Core	General Core	False	Epilepsy	Epilepsy
F1105-C00312	C00312	Body system category	Category or grouping used in the comprehensive assessment of a participant/subject, which includes a subjective history taking component as well as an objective based structured interview and physical examination of all the body systems	Supplemental	Physical Exam	False	Epilepsy	Epilepsy
F1807-C00007	C00007	Birth date	Date (and time, if applicable and known) the participant/subject was born	Core	General Core	False	Epilepsy	Epilepsy
F1106-C18504	C18504	Cranial nerves abnormality present text	The free-text field to explain the abnormality of the cranial nerve identified	Supplemental	Neurological Exam	False	Epilepsy	Epilepsy
F1122-C18571	C18571	Device implanted nerve stimulator new component model number	The model number of the new implanted nerve stimulator (INS) component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1120-C18558	C18558	Device implanted other adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to other Adverse Event (AE), specification	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1106-C18513	C18513	Sensory system abnormality dermatome present text	The free-text field to describe the dermatome sensory abnormality, the area of skin supplied with afferent nerve fibers by a single posterior spinal root	Supplemental	Neurological Exam	False	Epilepsy	Epilepsy
F1122-C18580	C18580	Device implanted right lead revision component type	The modification of the right lead component including explant, replacement, and repositioning	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1115-C18533	C18533	Electroencephalography ictal onset periodic discharge pattern type	The periodic discharge wave pattern of the brain on electroencephalogram (EEG) during onset of ictal discharge	Supplemental	Scalp Electroencephalography (EEG)	False	Epilepsy	Epilepsy
F1121-C18556	C18556	Device implanted intolerable stimulation adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to intolerable stimulation related Adverse Event (AE), specification	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1122-C18556	C18556	Device implanted intolerable stimulation adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to intolerable stimulation related Adverse Event (AE), specification	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1102-C58607	C58607	Seizure epilepsy generalized subtype status	The element related to the degree to which a generalized seizure is present	Supplemental	Classification of Seizures	False	Epilepsy	Epilepsy
F1111-C18523	C18523	Imaging magnetoencephalography evoked field acquisition sampling frequency	The number of samples per second (or per other unit) taken from a continuous signal to make a discrete signal using evoked field acquisition	Supplemental	Magnetoencephalography (MEG) Acquisition	False	Epilepsy	Epilepsy
F1109-C18518	C18518	Brain laterality type	Brain laterality of interest	Supplemental	Functional Magnetic Resonance Imaging (fMRI)	False	Epilepsy	Epilepsy
F1102-C58589	C58589	Seizure focal impaired awareness motor present status	The status indicating the degree to which a motor/observable focal impaired awareness seizure is present	Supplemental	Classification of Seizures	False	Epilepsy	Epilepsy
F1102-C58597	C58597	Seizure focal onset atonic present status	The status indicating the degree to which a focal onset atonic seizure is present	Supplemental	Classification of Seizures	False	Epilepsy	Epilepsy
F1106-C18506	C18506	Muscle weakness myopathic weakness present text	The free-text field to describethe myopathic weakness present resultling in muscle weakness	Supplemental	Neurological Exam	False	Epilepsy	Epilepsy
F1122-C18572	C18572	Device implanted nerve stimulator new component registration number	The registration number of the new implanted nerve stimulator (INS) component	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1120-C18559	C18559	Device implanted serious adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to serious device adverse effect(s) specification	Supplemental	Implanted Devices Log	False	Epilepsy	Epilepsy
F1106-C18514	C18514	Sensory system abnormality participant description text	The free-text field to capture the participant's description of the sensory abnormality	Supplemental	Neurological Exam	False	Epilepsy	Epilepsy
F1122-C18582	C18582	Device revision replacement log line number	The referenced line number of the entry on the device revision replacment log	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1115-C18534	C18534	Electroencephalography interictal epileptiform no localized onset description text	The free-text field to describe the nonlocalized onset of interictal epileptiform	Supplemental	Scalp Electroencephalography (EEG)	False	Epilepsy	Epilepsy
F1121-C18558	C18558	Device implanted other adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to other Adverse Event (AE), specification	Supplemental	Devices Log	False	Epilepsy	Epilepsy
F1122-C18558	C18558	Device implanted other adverse effect modification description text	The reason for modification of original parameters or original electrode configuration of implanted device due to other Adverse Event (AE), specification	Supplemental	Device Revision/Replacement Log	False	Epilepsy	Epilepsy
F1111-C18524	C18524	Imaging magnetoencephalography evoked field acquisition sedation type	Indicates type of sedative drugs were used to facilitate magnetoencephalography (MEG) acquisition	Supplemental	Magnetoencephalography (MEG) Acquisition	False	Epilepsy	Epilepsy

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The NINDS CDE Team does not post proprietary instruments/scales recommended by the CDE Working Groups on this website. This includes, but is not limited to, copyrighted or trademarked instruments/scales. Information about recommended instruments can be found in the Notice of Copyright (NOC) documents under ‘CRF Module/Guideline’ on each disorder’s data standards page. For any questions regarding these instruments/scales please contact the corresponding owner/author. The NINDS CDE Team is not responsible for the availability or content of these external sites, nor does the NINDS CDE Team endorse, warrant or guarantee the products, services or information described or offered at these other internet sites.