Centering equity through in-person data collection: short report.

Background During the COVID-19 pandemic, data collection activities largely became tele-remote, excluding those who did not have the required technology or digital literacy. Methods Between June and September 2020, we collected data in-person from people who use opioids in New York City. Participant...

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Bibliographic Details
Published in:Journal of Public Health Vol. 47; no. 2; pp. 375 - 380
Main Authors: Zaidi, Izza, Gomez, Leonardo Dominguez, Jordan, Ashly E, Jessell, Lauren, Harocopos, Alex
Format: research tables/charts Journal Article
Published: Oxford University Press / USA Jun2025
Online Access:View this record in EBSCOhost
Description
Summary:Background During the COVID-19 pandemic, data collection activities largely became tele-remote, excluding those who did not have the required technology or digital literacy. Methods Between June and September 2020, we collected data in-person from people who use opioids in New York City. Participants were recruited via street intercept and outside four syringe service programs in the city. Surveys were conducted outdoors, with researchers and participants wearing masks and maintaining physical distance. Results A total of 329 people participated in the survey. Participants reported an average age of 45.8 years, 69.6% identified as male, 32.6% identified as Hispanic/Latino/a and 22.3% identified as Black. Many experienced unstable housing/street homelessness (65.9%) and half did not have regular smartphone access (51.1%). Conclusion Many participants were struggling to meet their basic needs and did not have the resources to participate in tele-remote research or surveillance. In-person engagement may help researchers build trust, explain data security measures, and decrease technology and comprehension barriers. As data inform policies and programs, researchers must center equity by including under-engaged groups in data collection activities.