Testing a Mammography Decision Intervention in a Rural Setting

ConditionBreast Cancer
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age39-49
SponsorDartmouth-Hitchcock Medical Center

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 primary care providers (PCPs) practicing in rural settings. In consultation with patients, PCPs, and informatics experts, the study team will refine site selection, randomization, patient and PCP recruitment, and data collection protocols to meet the needs of the rural health care delivery system and participants. The result of this aim will be a modified protocol and intervention strategy that is acceptable to partners. (2) Adapt and test trial and intervention implementation features to achieve protocol acceptance and adherence. The investigators will pilot the adapted three-arm randomized trial protocol in rural primary care settings that compares the MyMammogram DA with or without a risk summary provided to the PCP pre-visit, relative to usual care. Implementing the trial in two phases (n=15 each) will systematically identify barriers and facilitators to trial participation to refine protocols. Participants will receive acceptability surveys and investigators will conduct qualitative interviews with patients and PCPs to understand experiences with trial implementation from multiple perspectives.

Eligibility criteria

Qualifiers

Females

Aged 39-49

Upcoming appointment with a participating primary care provider (within 4 weeks)

English or Spanish-speaking

Disqualifiers

Personal history of breast cancer (including lobular carcinoma in situ and ductal carcinoma in situ or atypical hyperplasia)

Mammogram in the prior 12 months

Trial design

Treatments tested in this trial

  • MyMammogram
  • Provider communication

Treatment groups

39 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Dartmouth-Hitchcock Medical Center

Lead sponsor

Trustees of Dartmouth College

Collaborator