Table 2.
Terms and definitions.
| Term | Definition |
|---|---|
| Digital literacy | The ability to find, use, and compose information through digital platforms |
| Social justice | Fairness, especially in how people are treated, what opportunities they have, and how decisions are made |
| Digital health social justice | The equitable opportunity for everyone to access, use, and benefit from digital health, to achieve their greatest standard of health and wellbeing. |
| Digital health | The use of apps, text-messaging and online interventions for health |
| Equity | A situation in which resources are distributed and tailored to the needs of the recipients. |
| Equality | A situation in which everyone has the same resources available to them. |
| Community-based participatory research (CBPR) | A research approach that involves partnerships between academic institutions, community-based organizations and community participants (10). |
| Digital intervention | A strategy to decrease delay in receiving help and advice as well as to improve treatment strategies to be evidence-based. |
| Social justice point of view | Utilizing social justice as the primary lens and objective to analyze the scenario, case, project, or research at hand |
| Community | A group of individuals that share some commonalities. This can be based on common characteristics (such as place of living, affinity, affiliation, demographics) or by the sheer bond between the individuals. |
| Social justice framework | A perspective that enables evaluation of a scenario to limit inequity and empowering those who are involved. |
| Human centered design | An approach consisting of one-on-one interviews, brainstorming sessions, and prototype testing with community members. |
| Social determinants of health | An individuals' social and/or structural environment, including education, employment and poverty |
| Open source | Software that is made available to the greater public, usually under a license, that gives anyone the freedom to use, change, and study it. |
| De-identification of Data | The removal of identifiable information to mitigate privacy breaches. |
| Algorithm | A process that is usually on the computer that calculates |
| Informed consent | An agreement with open communication between patient and practitioner for the patient to undergo a medical procedure or participate in a study. |
| Representation | A study has ample ”representation” in its study participant pool if individuals of different characteristics are sufficiently present in the pool. |
| Data return | Returning data taken of participants of a study or project to those individuals to benefit and empower them. |
| Unintended consequences | The materialization of consequences that were not foreseen by researchers or project teams. |