CompletedNot Applicable

Behavioral and Psychological Impact of Returning Breast Density Results to Latinas

United States1,386 participantsStarted 2016-10-27

Plain-language summary

This study will examine behavioral and psychological outcomes of breast density notification using a 3-group randomized design comparing usual written notification to two educationally enhanced approaches.

Who can participate

Age range40 Years – 74 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Female * Attending screening mammography at Mountain Park Health Center * Speak English or Spanish Exclusion Criteria: * Male * Current diagnosis of breast cancer

What they're measuring

Knowledge of Breast Density as a Masking Factor at First Follow-up

Timeframe: Baseline (T0) to first follow-up (T1, 2 weeks to 180 days from education end)

Anxiety Short Term (Baseline T0 to First Follow-up T1)

Timeframe: Change from baseline anxiety (T0) to T1: 2 weeks to 180 days after education end

BC Risk Assessment - Survey

Timeframe: T0 (baseline) to T1 (14 to 180 days after completion of education)

Trial details

NCT IDNCT02910986

SponsorMayo Clinic

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-11-15

Results submitted2023-11-16

View on ClinicalTrials.gov More Breast Cancer trials