Can we talk about epigenetics without causing confusion or harm?
NCT ID NCT07713667
First seen Jul 20, 2026 · Last updated Jul 21, 2026 · Updated 1 time
Summary
This study explores how to communicate about epigenetics — the process by which environment and lifestyle can turn genes on or off — in a way that is understandable and does not create ethical or social problems. Researchers will show different videos about epigenetics to 1,000 healthy adults from diverse backgrounds and measure their understanding and reactions. The goal is to find communication strategies that inform without misleading or stigmatizing.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this work could help scientists and doctors communicate about epigenetics in a way that is clear, accurate, and does not cause unnecessary worry or stigma.
- What could go wrong
- This is a behavioral study, not a medical treatment. The findings may not apply to all communities or real-world settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 1,000 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * English language speaker, Identify as one of five racial/ethnic groups: 1. Non-Hispanic White 2. Non-Hispanic Black, 3. Non-Hispanic Asian 4. Non-Hispanic Indigenous (i.e., Alaska Native/Native Hawaiians/American Indian/Other Pacific Islander) 5. Hispanic (all races) Exclusion Criteria: * Self-identify as a genetics expert
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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