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Testing a Mammography Decision Intervention in a Rural Setting

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 4 months later across 2 updates Sep 15, 2026 → Jan 20, 2027
See other at-risk trials from Dartmouth-Hitchcock Medical Center

Record History

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  1. Minor Eligibility criteria revised
  2. Minor Primary completion pushed from Nov 15, 2026 to Jan 20, 2027
    • Study completion pushed from Dec 15, 2026 to Jan 20, 2027
    • Eligibility criteria expanded, about 6 words
  3. Minor Primary completion pushed from Sep 15, 2026 to Nov 15, 2026
    • Study completion pushed from Sep 15, 2026 to Dec 15, 2026
    v7
  4. Minor Study sites: 1 to 3v6
  5. Minor Primary and study completion dates: May 1, 2026 to Sep 15, 2026v5
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  1. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Primary and study completion dates: Apr 1, 2026 to May 1, 2026
    v4
  2. Notable Start date: May 1, 2025 to Sep 1, 2025
    • Primary and study completion dates: Dec 1, 2025 to Apr 1, 2026
    v3
  3. Notable Primary endpoint revisedv2 Show 5 more changesShow less
    • Primary and study completion dates: Dec 2025 to Dec 1, 2025
    • Start date: May 2025 to May 1, 2025
    • Eligibility criteria expanded, about 22 words
    • Study description expanded, about 226 words
    • Secondary endpoints expanded, about 4 words
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT06522568
Lead Sponsor Dartmouth-Hitchcock Medical Center
Collaborators: Trustees of Dartmouth College
Conditions
(from sponsor)
Breast Cancer
Related terms Breast Neoplasms
Enrollment 39 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov