Can a digital guide empower women in polluted communities to make informed mammogram choices?
NCT ID NCT06098118
First seen Aug 18, 2026 · Last updated Aug 19, 2026 · Updated 1 time
Summary
This study tests an adapted online decision aid, called MyMammogram, designed to help women aged 39-49 who live in communities with PFAS contamination make informed choices about breast cancer screening. The tool provides personalized risk assessment, information on mammography benefits and risks, and helps clarify personal values. The goal is to see if the aid is acceptable and improves knowledge and decision-making about screening in a population with heightened environmental concerns.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- MyMammogram decision aid (an online breast cancer screening decision aid)
- What this could lead to
- If successful, this could provide a tailored tool to help women in PFAS-contaminated communities make informed breast cancer screening decisions, potentially reducing anxiety and improving decision quality.
- What could go wrong
- This is a small, early-stage study focused on decision-making, not on health outcomes. The decision aid may not change actual screening behavior or may not be generalizable to other communities.
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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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100 people
The number who actually took part.
- Started
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May 2024
- Finished
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Dec 2024
- 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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39 to 49 years
- Sex
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Female participants only
- 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: * Females aged 39-49 * No personal history of breast cancer, * No mammogram in the prior 12 months * Resident of Merrimack, Hillsborough, Rockingham or Bennington counties Exclusion Criteria: * History of breast cancer, ductal carcinoma in situ, lobular carcinoma in situ * Cognitive impairment impeding the ability to provide informed consent
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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.
Contacts and locations
Locations
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Dartmouth College
Hanover, New Hampshire, 03755, United States
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Other studies related to the condition(s) this trial covers.
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