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

# Question Options
1 What 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
2 Does the study use randomization? Individual, Cluster, Stepped-wedge, No randomization, Not applicable
3 What type of intervention or exposure? Therapeutic, Diagnostic, Medical device, Behavioral/lifestyle, Genetic/genomic, Educational/simulation, Digital therapeutics/mHealth, None (observational), Multiple/mixed
4 What is the temporal design? Prospective, Retrospective, Cross-sectional, Mixed
5 Is there a control or comparison group? Concurrent control, Historical controls, Self-controlled, No control
6 What best describes the participants? Human patients, Healthy volunteers, Students/trainees, Animals, Population-level data, Registry-based, Case report(s), Cells/tissues, Not applicable
7 What 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

Conditions Study type Confidence
Individual randomization + therapeutic intervention Randomized Controlled Trial (RCT) 95
Individual randomization + behavioral intervention Pragmatic Trial 85
Individual randomization (other) Randomized Controlled Trial (RCT) 90
Cluster randomization Cluster Randomized Trial 95
Stepped-wedge Stepped Wedge Trial 95
No randomization Quasi-Experimental Study 85
Self-controlled N-of-1 Trial 90
Animal subjects Animal Experiment 95
Cells/tissues In-Vitro / Translational Research 90
Registry participants Registry-Based Study 85

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


Determination logic: Observational approach

Conditions Study type Confidence
Comparative-effectiveness analysis Observational CER 95 (97 with comparison groups)
Registry participants Registry-Based Study 90
Prospective timing Cohort Study 90
Retrospective + control group Case-Control Study 90
Retrospective, no control Retrospective Cohort Study 85
Cross-sectional timing Cross-Sectional Study 95
Case report(s) + no control Case Report 90
Case report(s) + control Case Series 90
Population-level data Ecological Study 90
Diagnostic intervention Diagnostic Accuracy Study 90
Cells/tissues In-Vitro / Translational Research 90

Determination logic: Other approaches

Approach (+ refinements) Study type Confidence
Review Systematic Review & Meta-Analysis 95
Review + economic analysis Health Technology Assessment 85
Safety monitoring Pharmacovigilance / Adverse Event Reporting 95
Qualitative Qualitative Study 95
Qualitative + mixed analysis Mixed Methods Study 90
Modeling Modeling and Simulation Studies 85
Modeling + economic Economic Evaluation Study 90
Educational Simulation-Based Clinical Education 95 (98 with students)
AI/ML AI / Machine Learning Study 98 (99 with AI/ML analysis)
Wearable monitoring Real-Time Monitoring / Wearable Device Study 98 (99 with device)
PMS Post-Market Surveillance Study 98 (99 with device)
Big data Big Data / Secondary Data Analysis 98 (99 if retrospective)
Precision medicine Precision Medicine / Omics Integration 98 (99 with genomic analysis)

Cross-cutting override rules

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

Conditions Override study type Confidence
Device + prospective + observational Post-Market Clinical Follow-Up (PMCF) 85
Device + observational + human patients Real World Evidence Study 80
Economic analysis (not modeling) Economic Evaluation Study 85
Individual randomization + mixed analysis Adaptive Trial 75
Genomic analysis OR genetic intervention Genomic / Genetic Research 90
Educational + student/trainee participants Simulation-Based Clinical Education 95
AI/ML analysis AI / Machine Learning Study 95
Digital intervention Digital Therapeutics / mHealth Study 95 (97 if experimental)
Comparative-effectiveness + observational Observational CER 96

Default fallback

If no rule matches decisively:

Fallback Confidence Reasoning
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:

Field Contents
studyType The determined study type (selects the checklist)
confidence 0-100 value reflecting decisiveness
reasoning List 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.