Natural History of the Human Biological Response to Environmental Exposure and Injury

Launched by NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES (NIEHS) · May 14, 2021

Keywords

ClinConnect Summary

This clinical trial is studying how different environmental factors, like pollution, diet, and stress, can cause or worsen diseases in people. The goal is to understand the biological response to these exposures and how they lead to inflammation and other health issues. Researchers will collect various samples from participants, such as blood, saliva, and even household dust, to analyze these factors. This information will help improve future studies on how the environment affects our health.

To be eligible for this study, you need to be at least 18 years old, healthy, and willing to participate in the procedures, which include answering health questions and providing samples. The study is open to everyone, regardless of gender. Participants can expect to take part in one or more visits where they may give samples and complete surveys about their health and lifestyle. It's important to know that if you are currently pregnant or breastfeeding, or if you have certain health conditions, you won't be able to participate.

Gender

ALL

Eligibility criteria

• * INCLUSION CRITERIA:
• In order to be eligible to participate in this study, an individual must meet all of the following criteria:
• • 1. Stated willingness to comply with all study procedures and availability for the duration of the study.
• • 2. Ability to provide informed consent.
• • 3. Able to read and speak English.
• • 4. Male or female, aged greater than or equal to 18.
• • 5. Able to travel to the NIEHS CRU for study visits.
• EXCLUSION CRITERIA:
• An individual who meets any of the following criteria will be excluded from participation in this study:
• • 1. Not willing to have samples stored for future use.
• • 2. Current pregnancy or lactation, by participant verbal confirmation.
• • 3. Any condition that, in the investigator s opinion, places the participant at undue risk for complications associated with required study procedures.