Associations Between Household Mold Levels and Physical and Mental Health: A Mold and Mycotoxin Testing Research Registry
1 other identifier
observational
2,500
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2026
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 27, 2026
CompletedFirst Submitted
Initial submission to the registry
May 18, 2026
CompletedFirst Posted
Study publicly available on registry
May 22, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2029
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2029
May 22, 2026
May 1, 2026
2.9 years
May 18, 2026
May 18, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
PROMIS - Global Health
Ten questions assessing physical and mental health. Higher scores indicate superior physical and mental health.
Assessed at the time that the mold test is collected (cross-sectional)
Secondary Outcomes (2)
Mold-related symptoms
Assessed at the time that the mold test is collected (cross-sectional)
Mycotoxin levels
Assessed at the time that the mold test is collected (cross-sectional)
Interventions
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.
Eligibility 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.
You may qualify if:
- 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.
You may not qualify if:
- Dust Test users who do not provide informed consent for deidentified analysis and peer-reviewed publication of their data.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- OvationLablead
Study Sites (1)
OvationLab
Richmond, Virginia, 23220, United States
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 5 Years
- Sponsor Type
- NETWORK
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 18, 2026
First Posted
May 22, 2026
Study Start
April 27, 2026
Primary Completion (Estimated)
April 1, 2029
Study Completion (Estimated)
April 1, 2029
Last Updated
May 22, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will share
Mold results and participant-reported outcomes