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.
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