RecruitingNot ApplicableNCT06522568

Testing a Mammography Decision Intervention in a Rural Setting

Toward Optimization of a Mammography Decision Aid and Clinician Communication Intervention Trial for Rural Settings


Sponsor

Dartmouth-Hitchcock Medical Center

Enrollment

39 participants

Start Date

Sep 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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

Sex: FEMALEMin Age: 39 YearsMax Age: 49 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a decision-support tool to help women in rural areas make informed choices about whether to have mammogram screening for breast cancer, particularly for women in the 40–49 age group where guidelines differ. **You may be eligible if...** - You are female, aged 39–49 - You have an upcoming appointment with a primary care provider at a participating clinic (within 4 weeks) - You speak English or Spanish **You may NOT be eligible if...** - You have a personal history of breast cancer (including lobular or ductal carcinoma in situ, or atypical hyperplasia) - You had a mammogram in the past 12 months Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALMyMammogram

An online breast cancer screening decision aid

OTHERProvider communication

Provider will be provided with information from MyMammogram that includes patient's breast cancer risk and preferences for mammograms prior to the appointment


Locations(1)

Cheshire Medical Center

Keene, New Hampshire, United States

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NCT06522568


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