Testing a Mammography Decision Intervention in a Rural Setting

Recruiting N/A Interventional Study
Breast Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
39 – 49
Sex
Female
Study type
Interventional
Purpose
Prevention
Participants needed
39 (estimated)
Sponsor
Dartmouth-Hitchcock Medical Center · Other
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About This Trial
The overall objective of this COBRE pilot project is to enhance the design of a 3-arm cluster randomized trial that will test the efficacy and mechanism of effect of the MyMammogram DA with or without a provider communication intervention. This will be accomplished through two aims: (1) Refine, with community partner input, a clinical trial protocol to optimize engagement among patients and primar…
Trial Locations
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Eligibility Criteria
Patient Inclusion Criteria: * Females * Aged 39-49 * Upcoming appointment with a participating primary care provider (within 4 weeks) * English or Spanish-speaking Patient Exclusion Criteria: * Personal history of breast cancer (including lobular carcinoma in situ and ductal carcinoma in situ or …
Contacts

Christine M Gunn, PhD

603-646-5430

Christine.M.Gunn@dartmouth.edu

CONTACT