The Manuscript Survey & Checklist Determination

When you choose the guided-survey route, the module asks seven questions about your study and runs a rule-based determination to infer the study type and reporting checklist.

The logic is deterministic and rule-based (not a statistical model): each rule inspects your answers and, when its conditions match, sets the study type, a confidence value, and a reason. Later rules can override earlier ones, so order matters.


The seven survey questions

#QuestionOptions
1What is the primary study approach?Experimental, Observational, Systematic Review/Meta-Analysis, Qualitative, Modeling/Simulation, Safety Monitoring/Pharmacovigilance, Educational/Training, AI/Machine Learning, Real-Time Monitoring/Wearable, Post-Market Surveillance, Big Data/Secondary Data, Precision Medicine/Omics
2Does the study use randomization?Individual, Cluster, Stepped-wedge, No randomization, Not applicable
3What type of intervention or exposure?Therapeutic, Diagnostic, Medical device, Behavioral/lifestyle, Genetic/genomic, Educational/simulation, Digital therapeutics/mHealth, None (observational), Multiple/mixed
4What is the temporal design?Prospective, Retrospective, Cross-sectional, Mixed
5Is there a control or comparison group?Concurrent control, Historical controls, Self-controlled, No control
6What best describes the participants?Human patients, Healthy volunteers, Students/trainees, Animals, Population-level data, Registry-based, Case report(s), Cells/tissues, Not applicable
7What is the primary analysis approach?Quantitative, Qualitative thematic, Meta-analysis, Economic/cost-effectiveness, Genomic/bioinformatics, AI/ML, Comparative effectiveness, Mixed methods, Descriptive only

You answer in sequence and can step back to change an earlier answer.


Determination logic: Experimental approach

ConditionsStudy typeConfidence
Individual randomization + therapeutic interventionRandomized Controlled Trial (RCT)95
Individual randomization + behavioral interventionPragmatic Trial85
Individual randomization (other)Randomized Controlled Trial (RCT)90
Cluster randomizationCluster Randomized Trial95
Stepped-wedgeStepped Wedge Trial95
No randomizationQuasi-Experimental Study85
Self-controlledN-of-1 Trial90
Animal subjectsAnimal Experiment95
Cells/tissuesIn-Vitro / Translational Research90
Registry participantsRegistry-Based Study85

Participant-based rules (animals, cells/tissues, registry) override randomization rules.


Determination logic: Observational approach

ConditionsStudy typeConfidence
Comparative-effectiveness analysisObservational CER95 (97 with comparison groups)
Registry participantsRegistry-Based Study90
Prospective timingCohort Study90
Retrospective + control groupCase-Control Study90
Retrospective, no controlRetrospective Cohort Study85
Cross-sectional timingCross-Sectional Study95
Case report(s) + no controlCase Report90
Case report(s) + controlCase Series90
Population-level dataEcological Study90
Diagnostic interventionDiagnostic Accuracy Study90
Cells/tissuesIn-Vitro / Translational Research90

Determination logic: Other approaches

Approach (+ refinements)Study typeConfidence
ReviewSystematic Review & Meta-Analysis95
Review + economic analysisHealth Technology Assessment85
Safety monitoringPharmacovigilance / Adverse Event Reporting95
QualitativeQualitative Study95
Qualitative + mixed analysisMixed Methods Study90
ModelingModeling and Simulation Studies85
Modeling + economicEconomic Evaluation Study90
EducationalSimulation-Based Clinical Education95 (98 with students)
AI/MLAI / Machine Learning Study98 (99 with AI/ML analysis)
Wearable monitoringReal-Time Monitoring / Wearable Device Study98 (99 with device)
PMSPost-Market Surveillance Study98 (99 with device)
Big dataBig Data / Secondary Data Analysis98 (99 if retrospective)
Precision medicinePrecision Medicine / Omics Integration98 (99 with genomic analysis)

Cross-cutting override rules

After approach-based branches, cross-cutting rules can override regardless of approach chosen:

ConditionsOverride study typeConfidence
Device + prospective + observationalPost-Market Clinical Follow-Up (PMCF)85
Device + observational + human patientsReal World Evidence Study80
Economic analysis (not modeling)Economic Evaluation Study85
Individual randomization + mixed analysisAdaptive Trial75
Genomic analysis OR genetic interventionGenomic / Genetic Research90
Educational + student/trainee participantsSimulation-Based Clinical Education95
AI/ML analysisAI / Machine Learning Study95
Digital interventionDigital Therapeutics / mHealth Study95 (97 if experimental)
Comparative-effectiveness + observationalObservational CER96

Default fallback

If no rule matches decisively:

FallbackConfidenceReasoning
Randomized Controlled Trial (RCT)50"Default to RCT for unclear study design"

A confidence of 50 signals uncertainty -- consider using manual selection instead.


The recommendation output

The determination produces:

FieldContents
studyTypeThe determined study type (selects the checklist)
confidence0-100 value reflecting decisiveness
reasoningList of human-readable reasons showing the classification chain

The reasoning list accumulates from every rule that fired, showing not just the final classification but the characteristics that led to it. This lets you sanity-check the result and override with manual selection if needed.