The CONSORT Plus reporting requirements are organized into the above major groups. Listed in the tables below are the items that constitute the proposed Minimal Data Set. All RCT Bank entries must contain at least these items. The full CONSORT Plus guideline is available here.

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Click on Descriptor Name for an example of the item.


Administration

Heading

Required Items

Study Names

Study name

Investigators

Principal investigator name and institution

Ethics

 

Contact Person

Name of contact person

Funding

Funder names

Oversight Committees

 

Study Sites

Brief description of study sites

Stage of Trial

 

Study Design

Heading

Required Items

Objectives

Primary objective

Power/Sample Size Calculation

 

Statistical Analysis

 

Hypotheses

Primary hypothesis

A Priori Subgroups

Subgroup names and definitions

Post hoc Subgroups

Subgroup names and definitions

Study Monitoring

 

Protocol Changes

 

Why Study Stopped

Reason study stopped

Participants and Recruitment

Heading

Required Items

Inclusion Criteria

Inclusion criteria

Exclusion Criteria

Exclusion criteria

Recruitment

Source of participants

Participant Characteristics

Participant characteristics by intervention group

Treatment Assignment

Heading

Required Items

Randomization

 

Allocation Concealment

 

Assignment

 

Randomization Efficacy

Number of participants in each intervention group

Efficacy of Assignment Blinding

 

Interventions

Heading

Required Items

Experimental Intervention(s)

Drug Interventions

Procedures, Devices, or Behavorial Therapy

  • Name of procedure, device, or behavorial therapy[1]
  • If a device, manufacturer, make and model[1]
  • Description of intervention and its administration[1]

Organizational and Other Interventions (e.g., guidelines, education)

  • Description of intervention and its administration[1]

Comparison Intervention

Details of comparison intervention (as above)

Intervention Blinding

 

Efficacy of Intervention Blinding

 

Compliance

 

Crossovers

 

Treatment Completion

 

Cointerventions

 

Outcomes and Analysis

Heading

Required Items

Primary Outcome(s)

Name(s) and definition(s)

Secondary Outcome(s)

Name(s) and definition(s)

Baseline Characteristics

 

Side Effects

 

Outcome Assessment

Heading

Required Items

Outcome Assessment, Main Study Outcomes

 

Outcome Assessment, Side Effects

 

Schedule of Assessments

 

Followup

Heading

Required Items

Overall Followup

Number of participants having primary outcome(s) assessed at longest time point for each intervention group

Subgroup Followup

 

Results

Heading

Required Items

Main Outcome Results

Subgroup Results

 

Side Effects

 

Conclusions

 

Publications

Heading

Required Items

Trial Publications

Title, authors, and citation to main results paper

Publications Citing Trial

 

[1]Contact us, if you have an example of reporting this element.