Research Area Pathways

Decision pathways for each of the five research areas in the Navigator. After choosing jurisdiction and research area, these questions narrow toward a committee outcome.


Medicine and Health Sciences

The most detailed pathway. Separates by patient contact, then by intervention.

Patient contact question

AnswerRoutes to
No - Retrospective/Data Analysis OnlyScientific Research Ethics Committee
Yes - Direct Patient ContactIntervention question
Animal Research OnlyIACUC

Retrospective branch (all route to Scientific Research Ethics Committee)

  • Retrospective Chart/Medical Record Review
  • Database or Registry Analysis
  • Retrospective Imaging or Laboratory Data Analysis
  • Secondary Analysis of Existing Research Data

Intervention question

"Does your research involve any medical intervention that could alter patient outcomes?"

AnswerRoutes to
No - Observational/Data Collection OnlyNon-Interventional Clinical Research Ethics Committee
Yes - Medical Intervention InvolvedClinical Research Ethics Committee (jurisdiction-resolved)

Non-interventional study types

All route to Non-Interventional Clinical Research Ethics Committee:

  • Prospective Cohort Study
  • Prospective Case-Control Study
  • Cross-Sectional Study with Patient Contact
  • Clinical Attachment/Observation Study
  • Natural History Study
  • Patient Survey or Interview Study

Interventional studies

All route to Clinical Research Ethics Committee, resolved by jurisdiction (FDA = IRB-FDA, EMA = IEC-EMA).


Science and Engineering

Research type question

AnswerRoutes to
Human subjectsHuman-interaction question
Environmental researchEnvironmental-impact question
Laboratory researchHazardous-materials question
Engineering researchEngineering outcome
Computational/Data scienceData-science outcome

Human-subjects branch

"What type of human interaction?"

  • Physical measurements or testing - IRB/REB Required
  • Cognitive or behavioural testing - IRB/REB Required
  • Biological sample collection - IRB/REB Required

Environmental branch

"Scope of environmental impact?"

AnswerOutcome
SignificantEnvironmental Permits Required
ModerateStandard Permits Required
MinimalBasic Oversight Required

Laboratory branch

Sub-branches by type (Chemical/Biological/Physical), then hazardous materials level:

  • High-risk: Safety Permits Required
  • Moderate-risk: Safety Protocols Required
  • Low-risk: Basic Oversight Required

Education and Social Sciences

Research type question

AnswerRoutes to
Interviews or focus groupsInterview-type question
Observational studiesObservation-type question
Educational researchEducational Ethics Committee
Psychological researchPsychology outcome
Anthropological researchAnthropology outcome

Interview branch

Types: Individual interviews, Focus groups, Expert interviews

Follow-up: "Will you be working with vulnerable participants?"

OutcomeReview
Expert InterviewIRB/REB Required
Vulnerable Participants InterviewIRB/REB Full Board Review
Standard InterviewIRB/REB Required

Observation branch

Types: Participatory, Non-participatory, Online observation - all IRB/REB.

Educational branch

Types: Educational intervention, Educational assessment - route to Educational Ethics Committee.


Arts

Arts research type question

AnswerRoutes to
Performance or interactive artParticipant-involvement question
Cultural or heritage researchCultural-sensitivity question
Digital or new media artDigital-art sub-type
Visual artsVisual-arts outcome
Music researchMusic outcome

Performance branch

"How will participants be involved?"

InvolvementReview
Observation onlyEthics Approval Generally Not Required
Active participationIRB/REB Required
Vulnerable participantsIRB/REB Full Board Review Required

Cultural-sensitivity branch

Material typeOutcome
Indigenous cultural materialsIRB/REB and Community Approval Required
Religious or sacred artifactsEthics Approval Generally Not Required
Historical cultural heritageEthics Approval Generally Not Required
Contemporary cultural practicesIRB/REB Approval May Be Required

Indigenous materials require community approval in addition to institutional ethics review.


Survey Studies

Shortest pathway, keyed on anonymity and sensitivity.

Anonymity question

"Will survey responses be completely anonymous?"

If Yes - sensitivity question:

Sensitive data?Outcome
NoEthics Approval May Not Be Required
YesIRB/REB Approval Required

If No - identifiable data question:

Data typeOutcome
Personal identifiersIRB/REB Approval Required
Demographic data onlyIRB/REB Approval Likely Required

Anonymity plus non-sensitive content is the lowest-risk combination.


How pathways relate to committees

PathwayCommittee
Retrospective/secondary data (medicine)Scientific Research Ethics Committee
Patient contact, no interventionNon-Interventional Clinical Research Ethics Committee
Medical interventionClinical Research Ethics Committee (jurisdiction-resolved)
Animal researchIACUC
Human subjects (science, social, arts, survey)IRB / REB
Educational researchEducational Ethics Committee
Environmental researchNo ethics committee; environmental assessment, permits, monitoring, or standard safety oversight as applicable
Published-data-only / theoreticalNone

The outcome title tells you both the study classification and the review requirement. The result then provides committee requirements, regulatory references, and next steps.