Table 1 REP-EQUITY toolkit checklist

From: A toolkit for capturing a representative and equitable sample in health research

Section

REP-EQUITY question

Explanation

How this has been considered and addressed by the research team

Participant and site sampling

1. What are the relevant underserved groups?

Identify relevant groups and/or characteristics using available data33,34 and additional expertise28,32, depending on sites of interest or availability of sites27,32. Use this to inform and justify the choice of personal data to be collected from participants.

 

Objectives

2. What is the aim in relation to representativeness and equity?

Define the aim in terms of whether it is to test hypotheses about possible differences by underserved characteristic(s), generate hypotheses about possible differences by underserved characteristic(s), or ensure a just and equitable distribution of the risks and benefits of participation in research31.

 

Participant and site sampling

3. How will the sample proportion of individuals with underserved characteristics be defined?

Justify the chosen proportion in terms of comparability across studies, generalizability to population(s) of interest, distribution and equity impact of the risks and benefits of research participation, and feasibility of approach30.

 

Participant and site sampling

4. What are the recruitment goals?

Define recruitment goals in terms of requirements for statistical power calculations, exploratory analyses, generalizability30,31 and how they might be practically and ethically realized30.

 

Participant and site sampling

5. How will external factors be managed?

Formulate strategies to mediate external factors that may influence whether efforts to capture an equitable and representative sample can be realized30.

 

Analyses

6. How will representation be evaluated?

State the means for evaluation (for example, match with a priori recruitment goal30,31 or available data, compare to available data to establish the impact on equity in terms of burdens and benefits of research participation30,31).

 

Impact and dissemination

7. What will be the legacy?

Plan for lasting outputs (for example, advisory groups32, participant registries33, relationships with communities28,32); transparently report the use of the toolkit and data and/or findings relating to underserved groups.