Understanding how temperature affects health behaviors in Washington, DC
UrbanHEAT: Pilot of Prospective Observational Study of Health Behaviors, Outcomes, and Disparities in Individually Experienced Temperature Across an Urban Community
This study looks at how different temperatures affect the health habits and outcomes of people living in Washington, DC, by having them wear monitoring devices and answer surveys over two weeks.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 115 Years |
| Sex | All |
| Sponsor | National Institutes of Health Clinical Center (CC) NIH |
| Locations | 1 site (Bethesda, Maryland) |
| Trial ID | NCT06778252 on ClinicalTrials.gov |
What this trial studies
This observational study aims to explore the relationship between individually experienced temperature and various cardiometabolic risk behaviors and outcomes among residents of Washington, DC. Participants will engage in two remote visits to complete surveys and wear monitoring devices for two weeks to collect data on their physical activity, sleep, and stress levels. The study will also investigate disparities in temperature experiences based on demographic factors and assess the influence of environmental contexts on these experiences.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older living in Washington, DC, who can read and write in English and have access to a smartphone.
Not a fit: Patients who require hospitalization at enrollment or are unable to consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide insights into how temperature impacts health behaviors, potentially leading to targeted interventions for improving health outcomes in urban populations.
How similar studies have performed: While this study explores a novel approach to understanding temperature's impact on health behaviors, similar studies have shown success in linking environmental factors to health outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
* INCLUSION CRITERIA: In order to be eligible to participate in this study, an individual must meet all of the following criteria: * Stated willingness to comply with all study procedures and availability for the duration of the study. * Ability of subject to understand and the willingness to sign a written informed consent document. * Aged at least 18 years. * Ability to read and write in English. This is justified by the novelty of the survey instruments (e.g., momentary thermal comfort conducted in an ecological momentary assessment context). * Home address in Washington, DC * Availability of a smart phone on which Metricwire Ecological Momentary Assessment software can be downloaded and used during the 14-day data collection period. EXCLUSION CRITERIA: An individual who meets any of the following criteria will be excluded from participation in this study: * Requirement of hospitalization at enrollment. * Inability to consent. * Unwillingness to comply with study procedures.
Where this trial is running
Bethesda, Maryland
- National Institute on Minority Health and Health Disparities — Bethesda, Maryland, United States (Recruiting)
Study contacts
- Principal investigator: Kelly Jones — National Institute on Minority Health and Health Disparities (NIMHD)
- Study coordinator: Kelly Jones
- Email: kelly.jones2@nih.gov
- Phone: (240) 255-8340
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.