R5StudyDesignForR4

Cross-version ValueSet R5.StudyDesign for use in FHIR R4

activeExtensions for Using Data Elements from FHIR R5 in FHIR R40.1.072 concepts72 expanded

This cross-version ValueSet represents content from `http://hl7.org/fhir/ValueSet/study-design|5.0.0` for use in FHIR R4.

Metadata

hl7.org/fhir
Canonical URL
http://hl7.org/fhir/uv/xver/ValueSet/R5-study-design-for-R4
ID
R5-study-design-for-R4
Name
R5StudyDesignForR4

http://hl7.org/fhir/study-design

5.0.072 codes
CodeDisplay
SEVCO:01001Interventional research
SEVCO:01002Observational research
SEVCO:01003randomized assignment
SEVCO:01004Quasi-Randomized assignment
SEVCO:01005Non-randomized assignment
SEVCO:01006simple randomization
SEVCO:01007stratified randomization
SEVCO:01008block randomization
SEVCO:01009adaptive randomization
SEVCO:01010Comparative study design
SEVCO:01011Parallel cohort design
SEVCO:01012Crossover cohort design
SEVCO:01013Case control design
SEVCO:01014Matching for comparison
SEVCO:01015Cluster as unit of allocation
SEVCO:01016Uncontrolled cohort design
SEVCO:01017Case report
SEVCO:01018Time series design
SEVCO:01019Before and after comparison
SEVCO:01020Family study design
SEVCO:01021Twin study design
SEVCO:01022Population-based design
SEVCO:01023Non-comparative study design
SEVCO:01024Controlled crossover cohort design
SEVCO:01025Single-arm crossover design
SEVCO:01026Real world data collection
SEVCO:01027Cross sectional data collection
SEVCO:01028Longitudinal data collection
SEVCO:01029Clinical trial
SEVCO:01030Phase 1 trial
SEVCO:01031Exploratory investigational new drug study
SEVCO:01032Phase 1/Phase 2 trial
SEVCO:01033Phase 2 trial
SEVCO:01034Phase 2/Phase 3 trial
SEVCO:01035Phase 3 Trial
SEVCO:01036Post-marketing study
SEVCO:01037Post-Marketing Surveillance study
SEVCO:01038Expanded Access study
SEVCO:01039Real world data collection from healthcare records
SEVCO:01040Real world data collection from healthcare financing records
SEVCO:01041Pragmatic clinical trial
SEVCO:01042Secondary data collection from a registry
SEVCO:01043Multicentric
SEVCO:01044Ecological design
SEVCO:01045Primary data collection
SEVCO:01046Real world data collection from monitoring procedures
SEVCO:01048Real world data collection from testing procedures
SEVCO:01049Secondary data collection from prior research
SEVCO:01050Real world data collection from personal health records
SEVCO:01051Multisite data collection
SEVCO:01052Includes patient-reported outcome
SEVCO:01053Includes patient-centered outcome
SEVCO:01054Includes disease-oriented outcome
SEVCO:01060Blinding of study participants
SEVCO:01061Blinding of intervention providers
SEVCO:01062Blinding of outcome assessors
SEVCO:01063Blinding of data analysts
SEVCO:01064Allocation concealment
SEVCO:01085Includes process measure
SEVCO:01086Quantitative analysis
SEVCO:01087Qualitative analysis
SEVCO:01088Comparison Goal
SEVCO:01089Study Goal
SEVCO:01090Comparative Efficacy Goal
SEVCO:01091Comparative Effectiveness Goal
SEVCO:01092Comparative Safety Goal
SEVCO:01093Equivalence Goal
SEVCO:01094Non-inferiority Goal
SEVCO:01095Superiority Goal
SEVCO:01096Evaluation Goal
SEVCO:01097Derivation Goal
SEVCO:01098Validation Goal