The goal of the study is to compare a mind body intervention against usual care in patients with fatigue with mold illness. Our research questions include: * Is the mind body intervention additive to usual care in mold illness * Can the mind body intervention change self-reported overall wellness, and wearable device metrics such as heart rate variability
Age range
18 Years – 80 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Mold IQ Questionnaire
Timeframe: Baseline (Week 0) to post-intervention (Week 12)
Heart Rate Variability
Timeframe: Baseline (Week 0) to post-intervention (Week 12)