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 1001 - 1025 of 1122

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
F2620-C55775	C55775	Imaging ictal pain intensity value	The value related to the intensity of the subject's pain if the timing is ictal	Supplemental	Quantitative Sensory Testing (QST)	False	Headache	Headache
F2620-C15911	C15911	Quantitative sensory testing outcome type	Type of QST outcome being measured	Supplemental	Quantitative Sensory Testing (QST)	False	Headache	Headache
F2620-C15921	C15921	Quantitative sensory testing maximum stimulation intensity value	Measure of the maximum level of stimulation used during the testing	Supplemental	Quantitative Sensory Testing (QST)	False	Headache	Headache
F2620-C15929	C15929	Quantitative sensory testing stimulus duration	Duration of stimulus used during testing	Supplemental	Quantitative Sensory Testing (QST)	False	Headache	Headache
F2620-C18022	C18022	Data point exceed safety parameter description text	Description specifying how the data points that exceeded the safety parameters were handled statistically	Supplemental	Quantitative Sensory Testing (QST)	False	Headache	Headache
F2620-C55776	C55776	Imaging ictal headache since onset duration	The duration of time since the onset of the subject's headache if it was ictal	Supplemental	Quantitative Sensory Testing (QST)	False	Headache	Headache
F2620-C15912	C15912	Quantitative sensory testing outcome text	Definition of the QST outcome(s) chosen	Supplemental	Quantitative Sensory Testing (QST)	False	Headache	Headache
F2620-C15922	C15922	Quantitative sensory testing maximum stimulus duration	Maximum duration of stimuli used during the testing	Supplemental	Quantitative Sensory Testing (QST)	False	Headache	Headache
F2620-C15930	C15930	Quantitative sensory testing stimulus duration unit of measure	The units used to measure duration of stimuli	Supplemental	Quantitative Sensory Testing (QST)	False	Headache	Headache
F2620-C18023	C18023	Pain intensity stimulation result	Scale of 0-10 used to measure the intensity of the pain resulting from stimulation	Supplemental	Quantitative Sensory Testing (QST)	False	Headache	Headache
F2620-C55777	C55777	Imaging inter peri ictal headache since end duration	The duration of time since the end of the subject's last inter-ictal or peri-ictal headahe	Supplemental	Quantitative Sensory Testing (QST)	False	Headache	Headache
F2618-C18737	C18737	Medication prior or concomitant route type other text	The free-text field related to 'Medication prior or concomitant route type', specifying other text. Type of access route for the administration of the prior/concomitant medication	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C02013	C02013	Medication prior or concomitant dose unit of measure UCUM code	Code that represents the dosage unit of measure of the prior or concomitant medication administered. Unified Code for Units of Measure (UCUM)	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C22804	C22804	Pain present eleven point intensity scale	Scale for the participant's current pain intensity based on an a scale of 0-10	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C02014	C02014	Medication prior or concomitant name	Name of the prior/concomitant agent or drug administered	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C56039	C56039	Headache migraine rescue device used name	The name of the rescue device used in the treatment of headache or migraine	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C02015	C02015	Medication prior or concomitant route type	Type of access route for the administration of the prior/concomitant medication	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C56040	C56040	Headache migraine rescue device used start date	The start date on which the rescue device was used in the treatment of headache or migraine	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C02016	C02016	Medication prior or concomitant start date and time	The date (and time, if applicable and known) on which the prior/concomitant medication usage began	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C56041	C56041	Headache migraine rescue device used end date	The end date on which the rescue device was used in the treatment of headache or migraine	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C02025	C02025	Medication prior or concomitant RXNorm code	Code for name of the prior/concomitant agent or drug administered	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C05122	C05122	Study therapy administered date and time	Date (and time, if applicable and known) the study therapy was administered to the participant/subject	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C56042	C56042	Headache severity scale	The scale of the amount of headache the participant/subject is experiencing	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C16211	C16211	Headache pain medication after study drug indicator	Indicator whether the subject has received any additional pain or headache medications after the study drug was administered	Supplemental	Rescue Treatments	False	Headache	Headache
F2618-C18736	C18736	Medication prior or concomitant dose unit of measure other text	The free-text field related to 'Medication prior or concomitant dose unit of measure', specifying other text. Dosage unit of measure of the prior or concomitant medication administered	Supplemental	Rescue Treatments	False	Headache	Headache

Displaying 1001 - 1025 of 1122

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.