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NCT07071415

Overdiagnosis and Breast Cancer Screening Decisions

Completed NA Last updated 29 October 2025
What this trial tests

NA trial testing Breast cancer screening decision aid -- low risk in Mammography Screening in 311 participants. Completed in 20 October 2025.

Timeline
19 August 2025
Primary endpoint
20 October 2025
20 October 2025

Quick facts

Lead sponsorYale University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposehealth services research
Enrollment311
Start date19 August 2025
Primary completion20 October 2025
Estimated completion20 October 2025
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Yale University

Who can join

70 and older, female only, with Mammography Screening or Geriatrics. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a survey-based study using an online panel. The goal of the study is to understand whether information about overdiagnosis influences breast cancer screening intention among older women. Participants are first asked a series of questions about breast cancer screening including their intention to continue screening, knowledge of screening, and beliefs about screening. They are then shown one of three videos about breast cancer screening that contain information about overdiagnosis or a fourth control video that is identical but contains no information about overdiagnosis. Participants are then again asked about screening intention, along with knowledge of screening, overdiagnosis, and questions around trust.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07071415.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing