Recruiting NCT07605078
Associations Between Household Mold Levels and Physical and Mental Health: A Mold and Mycotoxin Testing Research Registry
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Mold-specific quantitative PCR (MSQPCR) testing.
- Who it may be relevant to
- Registry conditions: Mold Illness, Mold or Dust Allergy. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
The primary purpose of this study is to evaluate cross-sectional associations between mold exposures identified with The Dust Test and self-reported physical health, emotional health, and medical diagnoses. In addition, associations between mold exposures and mycotoxin levels among users who have done mycotoxin lab testing will also be evaluated.
Interventions
- Other Mold-specific quantitative PCR (MSQPCR) testing
The Dust Test is mold-specific quantitative PCR (MSQPCR) analysis that is being utilized to evaluate the associations between household mold organisms and a variety of human health outcomes.
Primary outcome measures
- PROMIS - Global Health [Time frame: Assessed at the time that the mold test is collected (cross-sectional)]
Secondary outcome measures (2)
- Mold-related symptoms [Time frame: Assessed at the time that the mold test is collected (cross-sectional)]
- Mycotoxin levels [Time frame: Assessed at the time that the mold test is collected (cross-sectional)]
Eligibility criteria
Inclusion criteria
- All Dust Test users who provide informed consent for deidentified analysis and peer-reviewed publication of their data will be eligible to participate in the research registry.
Exclusion criteria
- Dust Test users who do not provide informed consent for deidentified analysis and peer-reviewed publication of their data.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
United States · 1 center
- OvationLab — Richmond
Identifiers
NCT: NCT07605078 · TDT - 001