All participants will read a decision aid (DA) communicating evidence about mammography screening benefits and harms. Participants' evaluations of that evidence will be assessed, along with their screening intentions and receipt of screening. Participants will be sent 3 surveys via email and a final brief survey conducted by email or phone. The four surveys will be collected 1) upon enrollment and prior to the primary care appointment; 2) following the primary care appointment; 3) 3 months after enrollment; 4) 1 year after enrollment. The final 2 surveys will offer an increased incentive to increase retention rates.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
REDS (Reactance, self-Exemption, Disbelief and Source derogation) reactions to mammography benefits
Timeframe: 12 months
REDS (Reactance, self-Exemption, Disbelief and Source derogation) reactions to mammography harms
Timeframe: 12 months
Screening intentions question
Timeframe: 12 months
Number of participants who receive screening in the study period
Timeframe: 12 months