MedPath

Promoting Informed Choice for Breast Cancer Screening

Active, not recruiting
Conditions
Breast Cancer
Interventions
Behavioral: Decision aid
Registration Number
NCT05376241
Lead Sponsor
University of Colorado, Denver
Brief Summary

Identify the prevalence and predictors of reactance, self-exemption, disbelief, source derogation in reaction to evidence about mammography benefits and harms, and consequences for decision-making and trust.

Detailed Description

In this study, the goal is to identify the prevalence and predictors of reactance, self-exemption, disbelief, and source derogation in reaction to evidence about mammography benefits and harms, and consequences for decision-making and trust. Research has not yet systematically identified the proportion of women who respond negatively (vs. positively) to evidence about the benefits and harms of mammography screening, or attempted to explain these responses by examining theory-driven predictors. The Investigator will develop and conduct a probability-based nationally representative survey in which mammography evidence is communicated using current best practices in risk communication. The Investigators will identify theory-driven predictors of negative and positive responses to that evidence, and identify consequences of these responses for screening decision-making and trust.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
Female
Target Recruitment
498
Inclusion Criteria
  • Female
  • Between 39-49 years of age
  • No history of breast cancer
  • No known BRCA 1/2 mutation
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Exclusion Criteria
  • Non-English or Spanish Speaking
  • Persons unable to provide informed consent (e.g. sever dementia or cognitive disability or illiterate
  • History of breast cancer
  • Known BRCA 1/2 mutation
Read More

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Women age 39-49 in the United StatesDecision aidThe group is women age 39-49 in the United States who receive a decision aid intervention. The intervention is a breast cancer screening decision aid with information about screening guidelines, breast cancer mortality reduction, false positives, overdiagnosis, and a personal breast cancer risk estimate.
Primary Outcome Measures
NameTimeMethod
Source derogation24 hours

In response to mammography evidence, feeling that the source of the evidence is not trustworthy or competent. 4 questions total, each on a 7 point Likert scale, with mean scores that range from 1 to 7. Higher mean score reflects more source derogation.

Reactance24 hours

In response to mammography evidence, feeling that the information is manipulative or biased. 4 questions total, each on a 7 point Likert scale, with mean scores that range from 1 to 7. Higher mean scores reflect greater reactance.

Disbelief24 hours

In response to mammography evidence, feeling that the evidence is not accurate or believable. 4 questions total, each on a 7 point Likert scale, with mean scores that range from 1 to 7. Higher mean score reflects more disbelief in the information.

Self exemption24 hours

Feeling that mammography evidence is not relevant to oneself.34 questions total, each on a 7 point Likert scale, with mean scores that range from 1 to 7. Higher mean scores indicate greater belief that the information is not self relevant.

Screening Intentions24 hours

Intentions to engage in mammography screening. Options will include: 1. I am planning to start/continue having regular mammograms this year. 2. I am planning to wait until I'm older but before age 50 to have my first/next mammogram. 3. I am planning to wait until I am 50 to have my first/next mammogram. 4. I am not planning to have a mammogram in the future at any age

Secondary Outcome Measures
NameTimeMethod
Mammography screening knowledge (adapted from Hersch et al., 2015)24 hours

10 items that assess knowledge about mammography benefits and harms such as overdiagnosis; calculated as proportion out of 10 correct. Higher scores reflect greater knowledge; assessed both pre vs. post receipt of screening decision aid

Medical mistrust scale (Eaton et al., 2015)24 hours

6 question scale that assesses mistrust in healthcare providers. Calculated as mean trust (range 1-low trust to 5-high trust). Assessed both pre and post receipt of screening decision aid to evaluate change

Trial Locations

Locations (1)

University of Colorado Hospital

🇺🇸

Aurora, Colorado, United States

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